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145 results for “cryptic lineage”
Figure 3 in Molecular data reveal cryptic lineages within the northeastern Atlantic and Mediterranean small mussel drills of the Ocinebrina edwardsii complex (Mollusca: Gastropoda: Muricidae)
Figure 3. Consensus tree of a final sample of 104 trees obtained by BEAST on the cytochrome oxidase subunit I (COI) alignment. The black bars on the right delimit the Molecular Operational Taxonolllmic Units (MOTUs) as defined by the three species delimitation methods employed [Automatic Barcode Gap Discovery (ABGD), Generalized Mixed Yule- Coalescent (GMYC) and TCS]. Posterior supports> 0.95 are reported, and only for the nodes subtending the MOTUs. Voucher shells for each MOTU are figured (shells not to scale). 3A, MOTUs A–C; 3B, MOTUs D1–H.
Figure 6. A–C, Potamonautes perlatus s.s in Disentangling the divergence and cladogenesis in the freshwater crab species (Potamonautidae: Potamonautes perlatus sensu lato) in the Cape Fold Mountains, South Africa, with the description of two novel cryptic lineages
Figure 6. A–C, Potamonautes perlatus s.s. male neotype (SAM A45755): A, left gonopod 1, anterior view; B, left gonopod 1 posterior view; C, left gonopod 2 posterior view. D–F, Potamonautes barbarai sp. nov. male holotype (SAM A41061): D, left gonopod 1, anterior view; E, left gonopod 1 posterior view; F, left gonopod 2 posterior view; and G–I, Potamonautes barnardi sp. nov. male holotype (SAM A41013): G, left gonopod 1, anterior view; H, left gonopod 1 posterior view; I, left gonopod 2 posterior view. Scale bars = 1.0 mm.
Figure 3. A in Disentangling the divergence and cladogenesis in the freshwater crab species (Potamonautidae: Potamonautes perlatus sensu lato) in the Cape Fold Mountains, South Africa, with the description of two novel cryptic lineages
Figure 3. A consensus Bayesian inference phylogram of Potamonautes perlatus s.l. from the combined nuDNA (28S rRNA) and mtDNA (cytochrome oxidase I and 16S rRNA) data sets as well as outgroups. Node support values are shown by maximum likelihood (ML) bootstrap values above and maximum parsimony (MP)/posterior probabilities of Bayesian inference (BI) below. Low bootstrap support (<75% for MP and ML) and posterior probability (<0.95 for BI) values are not shown. The * is indicative of nodes that are not statistically supported.
Figure 1. Sampling localities for Potamonautes perlatus s.l in Disentangling the divergence and cladogenesis in the freshwater crab species (Potamonautidae: Potamonautes perlatus sensu lato) in the Cape Fold Mountains, South Africa, with the description of two novel cryptic lineages
Figure 1. Sampling localities for Potamonautes perlatus s.l. along rivers occurring on the Cape Fold Mountains. The black circles with adjacent numbers represent localities (see Table 1 for names).
Figure 2. A in Disentangling the divergence and cladogenesis in the freshwater crab species (Potamonautidae: Potamonautes perlatus sensu lato) in the Cape Fold Mountains, South Africa, with the description of two novel cryptic lineages
Figure 2. A maximum likelihood (ML) phylogram of the combined mtDNA sequences for the phylogenetic reconstruction of Potamonautes perlatus s.l. The ML node support is shown by bootstrap values above each branch (only values above 75% are shown). The values below the branches are bootstrap values for maximum parsimony (MP)/posterior probabilities for Bayesian inference (BI; the * indicates no support). The numbers next to each taxon name represent the individual specimens; no numbering is given to taxa for which the entire population occurs on one branch.
Hyper-cryptic radiation of a tropical montane plant lineage
<p>Species are seen as the fundamental unit of biotic diversity, and thus their delimitation is crucial for defining measures for diversity assessments and studying evolution. Differences between species have traditionally been associated with variation in morphology. And yet, the discovery of cryptic diversity suggests that the evolution of distinct lineages does not necessarily involve trait differences. Here, we analyze 1,684,987 variant sites and over 4000 genes for more than 400 samples to show how a tropical montane plant lineage (<em>Geonoma</em> <em>undata</em> species complex) is composed of numerous unrecognized genetic groups that are not morphologically distinct. We find that 11 to 14 clades do not correspond to the three currently recognized species. Most clades are genetically independent and geographic distance and topography are the most important factors determining this genetic divergence. This lineage does not match the model of an adaptive radiation, but instead, constitutes the first example of a hyper-cryptic plant radiation in tropical mountains.</p>
Phylogeography of a widely distributed plant species reveals cryptic genetic lineages with parallel phenotypic responses to warming and drought conditions
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Data from: Asynchronous spawning in sympatric populations of a hard coral reveals cryptic species and ancient genetic lineages
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Data from: Genetics, morphology and ecology reveal a cryptic pika lineage in the Sikkim Himalaya
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Data from: Cryptic lineages in the Wolf Cardinalfish living in sympatry on remote coral atolls
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Data from: Strong selection against hybrids maintains a narrow contact zone between morphologically cryptic lineages in a rainforest lizard
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Luciferase readout: Raw neutralization results for neutralization assays from pseudoparticles containing the SARS-CoV-2 receptor binding domain from a cryptic lineage
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Data from: Cryptic divergent lineages of Pultenaea pauciflora M.B. Scott (Fabaceae, Mirbelieae) exhibit different evolutionary history
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Data from: Random interbreeding between cryptic lineages of the Common Raven: evidence for speciation in reverse
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Cryptic lineages respond differently to coral bleaching
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Data from: Separation in flowering time contributes to the maintenance of sympatric cryptic plant lineages
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Data from: Cryptic species diversity and reproductive isolation among sympatric lineages of Strongylocentrotus sea urchins in the northwest Atlantic
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Hyper-cryptic radiation of a tropical montane plant lineage
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Data from: Cryptic lineages of a common alpine mayfly show strong life-history divergence
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Data from: Parallel pattern of differentiation at a genomic island shared between clinal and mosaic hybrid zones in a complex of cryptic seahorse lineages
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