scholarly journals Interspecific and Intraspecific Genetic Diversity of Thunnus Species

Author(s):  
Mei-Chen Tseng ◽  
Chuen-Tan Jean ◽  
Peter J. ◽  
Yin-Huei Hung
2019 ◽  
Author(s):  
Jiaqi Wu ◽  
Takahiro Yonezawa ◽  
Hirohisa Kishino

AbstractWhat determines genetic diversity and how it connects to the various biological traits is unknown. In this work, we offer answers to these questions. By comparing genetic variation of 14,671 mammalian gene trees with thousands of individual genomes of human, chimpanzee, gorilla, mouse and dog/wolf, we found that intraspecific genetic diversity is determined by long-term molecular evolutionary rates, rather than de novo mutation rates. This relationship was established during the early stage of mammalian evolution. Expanding this new finding, we developed a method to detect fluctuations of species-specific selection on genes as the deviations of intra-species genetic diversity predicted from long-term rates. We show that the evolution of epithelial cells, rather than of connective tissue, mainly contributes to morphological evolution of different species. For humans, evolution of the immune system and selective sweeps subjected by infectious diseases are most representative of adaptive evolution.


2018 ◽  
Author(s):  
Vasco Elbrecht ◽  
Ecaterina Edith Vamos ◽  
Dirk Steinke ◽  
Florian Leese

Background. DNA metabarcoding is used to generate species composition data for entire communities. However, sequencing errors in high throughput sequencing instruments are fairly common, usually requiring reads to be clustered into operational taxonomic units (OTU), losing information on intraspecific diversity in the process. While COI haplotype information is limited in resolution, it is nevertheless useful in a phylogeographic context, helping to formulate hypothesis on taxon dispersal. Methods. This study combines sequence denoising strategies, normally applied in microbial research, with additional abundance-based filtering to extract haplotypes from freshwater macroinvertebrate metabarcoding data sets. This novel approach was added to the R package "JAMP" and can be applied to Cytochrome c oxidase subunit I (COI) amplicon datasets. We tested our haplotyping method by sequencing i) a single-species mock community composed of 31 individuals with different haplotypes spanning three orders of magnitude in biomass and ii) 18 monitoring samples each amplified with four different primer sets and two PCR replicates. Results. We detected all 15 haplotypes of the single specimens in the mock community with relaxed filtering and denoising settings. However, up to 480 additional unexpected haplotypes remained in both replicates. Rigorous filtering removes most unexpected haplotypes, but also can discard expected haplotypes mainly from the small specimens. In the monitoring samples, the different primer sets detected 177 - 200 OTUs, each containing an average of 2.40 to 3.30 haplotypes per OTU. Population structures were consistent between replicates, and similar between primer pairs, depending on the primer length. A closer look at abundant taxa in the data set revealed various population genetic patterns, e.g. Taeniopteryx nebulosa and Hydropsyche pellucidula with a difference in north-south haplotype distribution, while Oulimnius tuberculatus and Asellus aquaticus display no clear population pattern but differ in genetic diversity. Discussion. We developed a strategy to infer intraspecific genetic diversity from bulk invertebrate monitoring samples using metabarcoding data. It needs to be stressed that at this point metabarcoding-informed haplotyping is not capable of capture the full diversity present in such samples, due to variation in specimen size, primer bias and loss of sequence variants with low abundance. Nevertheless, for a high number of species intraspecific diversity was recovered, identifying potentially isolated populations and potential taxa for further more detailed phylogeographic investigation. While we are currently lacking large-scale metabarcoding data sets to fully take advantage of our new approach, metabarcoding-informed haplotyping holds great promise for biomonitoring efforts that not only seek information about biological diversity but also underlying genetic diversity.


Author(s):  
Jérôme G. Prunier ◽  
Mathieu Chevalier ◽  
Allan Raffard ◽  
Géraldine Loot ◽  
Nicolas Poulet ◽  
...  

AbstractTheory predicts that biodiversity is causally linked to key ecological functions such as biomass productivity, and that loss in functional traits both among- and within-species can reduce the efficiency of ecosystem functions. There has been ample empirical and experimental demonstration that species loss indeed reduces the efficiency of ecosystem functions, with tremendous impacts on services provided by biodiversity. Nonetheless, and despite the fact that within-species diversity is strongly altered by human activities, there have been little attempts to empirically test (i) whether intraspecific genetic diversity actually promotes productivity and stability in wild populations, and, (ii) if so, to quantify its relative importance compared to other determinants. Capitalizing on 20-year demographic surveys in wild fish populations, we show that genetic diversity does not increase mean biomass production in local populations, but strongly and consistently stabilizes biomass production over time. Genetic diversity accounts for about 20% of explained variance in biomass stability across species, an important contribution about half that of environment and demography (about 40% each). Populations having suffered from demographic bottlenecks in the recent past harbored lower levels of genetic diversity and showed less stability in biomass production over the last 20 years. Our study demonstrates that the loss of intraspecific genetic diversity can destabilize biomass productivity in natural vertebrate populations in just a few generations, strengthening the importance for human societies to adopt prominent environmental policies to favor all facets of biodiversity.


2018 ◽  
Author(s):  
Vasco Elbrecht ◽  
Ecaterina Edith Vamos ◽  
Dirk Steinke ◽  
Florian Leese

Background. DNA metabarcoding is used to generate species composition data for entire communities. However, sequencing errors in high throughput sequencing instruments are fairly common, usually requiring reads to be clustered into operational taxonomic units (OTU), losing information on intraspecific diversity in the process. While COI haplotype information is limited in resolution, it is nevertheless useful in a phylogeographic context, helping to formulate hypothesis on taxon dispersal. Methods. This study combines sequence denoising strategies, normally applied in microbial research, with additional abundance-based filtering to extract haplotypes from freshwater macroinvertebrate metabarcoding data sets. This novel approach was added to the R package "JAMP" and can be applied to Cytochrome c oxidase subunit I (COI) amplicon datasets. We tested our haplotyping method by sequencing i) a single-species mock community composed of 31 individuals with different haplotypes spanning three orders of magnitude in biomass and ii) 18 monitoring samples each amplified with four different primer sets and two PCR replicates. Results. We detected all 15 haplotypes of the single specimens in the mock community with relaxed filtering and denoising settings. However, up to 480 additional unexpected haplotypes remained in both replicates. Rigorous filtering removes most unexpected haplotypes, but also can discard expected haplotypes mainly from the small specimens. In the monitoring samples, the different primer sets detected 177 - 200 OTUs, each containing an average of 2.40 to 3.30 haplotypes per OTU. Population structures were consistent between replicates, and similar between primer pairs, depending on the primer length. A closer look at abundant taxa in the data set revealed various population genetic patterns, e.g. Taeniopteryx nebulosa and Hydropsyche pellucidula with a difference in north-south haplotype distribution, while Oulimnius tuberculatus and Asellus aquaticus display no clear population pattern but differ in genetic diversity. Discussion. We developed a strategy to infer intraspecific genetic diversity from bulk invertebrate monitoring samples using metabarcoding data. It needs to be stressed that at this point metabarcoding-informed haplotyping is not capable of capture the full diversity present in such samples, due to variation in specimen size, primer bias and loss of sequence variants with low abundance. Nevertheless, for a high number of species intraspecific diversity was recovered, identifying potentially isolated populations and potential taxa for further more detailed phylogeographic investigation. While we are currently lacking large-scale metabarcoding data sets to fully take advantage of our new approach, metabarcoding-informed haplotyping holds great promise for biomonitoring efforts that not only seek information about biological diversity but also underlying genetic diversity.


2014 ◽  
Vol 35 (2) ◽  
pp. 263-269 ◽  
Author(s):  
Evanthia Thanou ◽  
Sinos Giokas ◽  
Panagiotis Kornilios

Two slow worm species are distributed at the southernmost part of the Balkan Peninsula: Anguis cephallonica, an endemic of the Peloponnese and the islands Zakynthos, Ithaki and Kephallonia, and A. graeca. Here, we investigate the intraspecific genetic diversity of A. cephallonica from the Peloponnese and Kephallonia and analyse A. graeca, from the northern Peloponnese, where it is found in sympatry with A. cephallonica. MtDNA and nDNA phylogenetic analyses confirm the genetic similarity of Peloponnesian and Kephallonian populations of A. cephallonica and reveal significant mtDNA genetic variation within it, probably related to the occurrence of multiple subrefugia in the Peloponnese. Peloponnesian A. graeca populations are genetically similar to non-Peloponnesian conspecifics implying recent dispersal to the Peloponnese. In contrast to the genetic markers, morphological characteristics (such as the number of mid-body scale-rows) failed to distinguish between Peloponnesian A. cephallonica and A. graeca. Although the former species is believed to be well-differentiated from its congeneric taxa, a thorough morphological study is needed.


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