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1,104 results for “morphological variation”
Morphometric and phylogeny data for: Morphology, variation, and systematics of the late Cambrian Laurentian dikelocephalid trilobite Walcottaspis vanhornei
<p></p> <p><span>These pages provide details of the taxa, characters and character states used in the phylogenetic analyses of <em>Walcottaspis vanhornei </em></span><span>(Walcott, 1914)</span><span> </span><span>and relatives in the accompanying paper. <span> </span>Phylogenetic information included here provides details of characters and taxa used for both the parsimony-based and Bayesian analyses and documents levels of support of two types (Bremer and bootstrap) for the parsimony analysis. Also included here is the result of Bayesian maximum likelihood analysis that provides further support to the results of parsimony analysis. We include bivariate plots of the variance explained by each relative warp for the sclerites analyzed and morphometric measurement error analysis. </span></p>
Patterns of genetic variation and morphology support the recognition of five species in the Gaultheria leucocarpa Blume (Ericaceae) group from mainland China
<p><em>Gaultheria</em> <em>leucocarpa</em> and its varieties form a clade of aromatic shrubs that is widely distributed in subtropical and East Asian tropical regions. The group is taxonomically difficult and is in need of thorough taxonomic investigation. This study focused on taxonomic delimitation within the <em>G. leucocarpa </em>group from mainland China. Field surveys covering the distributional range of <em>G. leucocarpa</em> in mainland China were conducted, wherein four populations from Yunnan and one from Hunan were found bearing visibly morphological and habitat differences. A 63-species phylogenetic tree of <em>Gaultheria</em> based on one nuclear and three chloroplast markers that included samples from the <em>G. leucocarpa</em> group was reconstructed with maximum likelihood to clarify the monophyly of the <em>G. leucocarpa</em> group. Taxonomic relationships among populations of the <em>G. leucocarpa</em> group were investigated with morphology and population genetics, the latter by using two chloroplast genes and two low-copy nuclear genes. Based on the sum of morphological and genetic analyses, we described three species of <em>Gaultheria</em> as new to science, clarified the taxonomic status of <em>G. leucocarpa</em> var. <em>pingbienensis</em>, elevating it to the species level, and resurrected <em>G</em>. <em>crenulata</em> and treated the varieties <em>G. leucocarpa </em>var<em>. crenulata</em>, and <em>G. leucocarpa </em>var<em>. yunnanensis</em> as synonyms of this species. We provide a key to the five species now recognized, along with descriptions and photographs.</p>
Figure 7 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations
Figure 7. Phaea quadrimaculata Wappes & Santos-Silva, 2020. (A-E) Male from Mexico, Oaxaca: (A) Dorsal habitus; (B) Ventral habitus; (C) Abdominal ventrites; (D) Lateral habitus; (E) Head, frontal view. (F) Holotype female, abdominal ventrites.
Figure 1 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations
Figure 1. Xystochroma luteotarsis sp. nov. (A-E) Holotype male: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view; (E) Scape. (F-G) Paratype female: (F) Dorsal habitus; (G) Ventral habitus.
Figure 4 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations
Figure 4. Rosalba strandi (Breuning, 1943). (A-D) Male, specimen 1, from Paraguay: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view. (E) Male from Brazil (Minas Gerais, Serra do Caraça), dorsal habitus. (F-G) Female from Paraguay: (F) Dorsal habitus; (G) Ventral habitus. (H-J) Males from Paraguay, dorsal habitus: (H) specimen 2; (I) specimen 3; (J) specimen 4.
Figure 3 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations
Figure 3. Bisaltes (Bisaltes) lateralis sp. nov., holotype female: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view; (E) Scape.
Figure 2 in Expanding knowledge of American Cerambycidae (Coleoptera): new species, new records, and morphological variations
Figure 2. Psyrassa spp. (A-F) P. tysoni sp. nov., holotype female: (A) Dorsal habitus; (B) Ventral habitus; (C) Lateral habitus; (D) Head, frontal view; (E) Head, lateral view; (F) Procoxal cavities. (G-J) P. pertenuis (Casey, 1924), holotype: (G) Lateroventral view; (H) Dorsal habitus; (I) Head, frontal view; (J) Partial lateral habitus. Figures G, I, and J by Eugenio H. Nearns; figure H from Lingafelter et al. (2023).
Genetic and morphological data from two bird genera (Cranioleuca and Geospiza) showing continuous variation
<p class="MsoNormal">Extinction is a dominant force shaping patterns of biodiversity through time however its role as a catalyst of speciation has been overlooked. Here, we synthesize ideas alluded to by Darwin and others into the model of 'speciation-by-extinction' in which speciation results from the extinction of intermediate populations within a single geographically variable species. We explore the properties and distinguishing features of speciation-by-extinction with respect to other established speciation models. We demonstrate its plausibility by showing that the experimental extinction of populations within variable species can result in speciation. The prerequisites for speciation-by-extinction, geographically structured intraspecific variation and local extinction, are ubiquitous in nature, indicating that speciation-by-extinction may be a prevalent, but underappreciated, speciation mechanism.</p>
Intrasexual variations in arm morphology related to alternative reproductive tactics in Japanese spear squid
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Geometric morphometrics as a tool for evaluating Eublastoidea morphological variation
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Data from: Sugar-rich resources mediate geographic morphological variation in a dominant, neotropical savanna ant
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Data from: Seasonality and morphological variation shape intraspecific seed dispersal networks in gopher tortoises
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Genetic variation of morphological scaling in Drosophila
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A colonial epiphyte with a twist: Morphological variation and potential division of labour in the fern <em>Platycerium bifurcatum</em>
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Patterns of genetic variation and morphology support the recognition of five species in the Gaultheria leucocarpa Blume (Ericaceae) group from mainland China
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Variation in mouse pelvic morphology maps to locations enriched in Sox9 Class II and Pitx1 regulatory features
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Concordant patterns of morphological, stable isotope, and genetic variation in a recent ecological radiation (Salmonidae:Coregonus spp.)
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Ecologically-related variation of digit morphology in Cyrtodactylus (Gekkota, Squamata) reveals repeated origins of incipient adhesive toepads
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Ecological variation drives morphological differentiation in a highly social vertebrate
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Broad- and small-scale environmental gradients drive variation in chemical, but not morphological, leaf traits of vascular epiphytes
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Allen Brain Atlas
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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