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      Genomics overrules mitochondrial DNA, siding with morphology on a controversial case of species delimitation

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          Abstract

          Species delimitation is a major quest in biology and is essential for adequate management of the organismal diversity. A challenging example comprises the fish species of red snappers in the Western Atlantic. Red snappers have been traditionally recognized as two separate species based on morphology: Lutjanus campechanus (northern red snapper) and L. purpureus (southern red snapper). Recent genetic studies using mitochondrial markers, however, failed to delineate these nominal species, leading to the current lumping of the northern and southern populations into a single species ( L. campechanus ). This decision carries broad implications for conservation and management as red snappers have been commercially over-exploited across the Western Atlantic and are currently listed as vulnerable. To address this conflict, we examine genome-wide data collected throughout the range of the two species. Population genomics, phylogenetic and coalescent analyses favour the existence of two independent evolutionary lineages, a result that confirms the morphology-based delimitation scenario in agreement with conventional taxonomy. Despite finding evidence of introgression in geographically neighbouring populations in northern South America, our genomic analyses strongly support isolation and differentiation of these species, suggesting that the northern and southern red snappers should be treated as distinct taxonomic entities.

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          Cryptic species as a window on diversity and conservation.

          The taxonomic challenge posed by cryptic species (two or more distinct species classified as a single species) has been recognized for nearly 300 years, but the advent of relatively inexpensive and rapid DNA sequencing has given biologists a new tool for detecting and differentiating morphologically similar species. Here, we synthesize the literature on cryptic and sibling species and discuss trends in their discovery. However, a lack of systematic studies leaves many questions open, such as whether cryptic species are more common in particular habitats, latitudes or taxonomic groups. The discovery of cryptic species is likely to be non-random with regard to taxon and biome and, hence, could have profound implications for evolutionary theory, biogeography and conservation planning.
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            Restriction site-associated DNA sequencing, genotyping error estimation and de novo assembly optimization for population genetic inference.

            Restriction site-associated DNA sequencing (RADseq) provides researchers with the ability to record genetic polymorphism across thousands of loci for nonmodel organisms, potentially revolutionizing the field of molecular ecology. However, as with other genotyping methods, RADseq is prone to a number of sources of error that may have consequential effects for population genetic inferences, and these have received only limited attention in terms of the estimation and reporting of genotyping error rates. Here we use individual sample replicates, under the expectation of identical genotypes, to quantify genotyping error in the absence of a reference genome. We then use sample replicates to (i) optimize de novo assembly parameters within the program Stacks, by minimizing error and maximizing the retrieval of informative loci; and (ii) quantify error rates for loci, alleles and single-nucleotide polymorphisms. As an empirical example, we use a double-digest RAD data set of a nonmodel plant species, Berberis alpina, collected from high-altitude mountains in Mexico. © 2014 John Wiley & Sons Ltd.
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              TCS: estimating gene genealogies

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                Author and article information

                Journal
                Proceedings of the Royal Society B: Biological Sciences
                Proc. R. Soc. B
                The Royal Society
                0962-8452
                1471-2954
                April 03 2019
                April 10 2019
                April 03 2019
                April 10 2019
                : 286
                : 1900
                : 20182924
                Affiliations
                [1 ]Department of Biology, University of Puerto Rico, Río Piedras, PO Box 23360, San Juan, PR 00931, USA
                [2 ]Instituto de Estudos Costeiros, Laboratório de Genética Aplicada, Campus Bragança, Alameda Leandro Ribeiro, S/N, Aldeia, 68600-000 Bragança, Pará, Brazil
                [3 ]USFDA Center for Food Safety and Applied Nutrition, 5001 Campus Drive, College Park, MD 20740, USA
                [4 ]CONACYT Research Fellow – Comisión Nacional para el Conocimiento y Uso de la Biodiversidad, México, Liga Periférico – Insurgentes Sur, No. 4903, 14010, México, DF, México
                [5 ]Laboratorio de Biología Acuática, Facultad de Biología, Universidad Michoacana de San Nicolás de Hidalgo, Ciudad Universitaria, 58000, Morelia, Michoacán, México
                [6 ]North Carolina Wildlife Resources Commission, Raleigh, NC 27699-1700, USA
                [7 ]University of Florida, School of Forest Resources and Conservation, Program of Fisheries and Aquatic Sciences, Gainesville, FL 32653, USA
                [8 ]Florida Fish and Wildlife Research Institute, 100 8th Ave SE, St. Petersburg, FL 33701, USA
                [9 ]Florida Fish and Wildlife Conservation Commission, Farris Bryant Building, 620 S. Meridian St., Tallahassee, FL 32399-1600, USA
                [10 ]Computer Science Department, University of Puerto Rico, Río Piedras, PO Box 23360, San Juan, PR 00931, USA
                [11 ]Universidad del Magdalena, carrera 32 No. 22-08 Santa Marta, Magdalena, Colombia
                [12 ]Universidad Nacional de Colombia Sede Caribe Cecimar, El Rodadero, Santa Marta, Colombia
                [13 ]Instituto de Estudos Costeiros, Laboratório de Genética e Biologia Molecular, Universidade Federal do Pará, Campus Bragança, Alameda Leandro Ribeiro, S/N, Aldeia, 68600-000 Bragança, Pará, Brazil
                [14 ]Department of Biology, The University of Oklahoma, 730 Van Vleet Oval, Room 314, Norman, OK 73019, USA
                Article
                10.1098/rspb.2018.2924
                6501682
                30940064
                a252f81b-5620-404d-bb94-a1c1f90e0611
                © 2019
                History

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