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390 results for “Commensals”
Fig. 3 in Commensalism in the fossil record: Eunicid polychaete bioerosion on Pliocene solitary corals
Fig. 3. Polychaete trace fossil Sulcichnus maeandriformis on Flabellum sp. from different Lower Pliocene sites. Pairs of pictures correspond to both sides of a single corallite and show the specular symmetry of the boring. A. Paratype, MMPE/Ic001.003.001, Bizcornil, Estepona. B. Paratype, MMPE/Ic001. 002.001, Velerín, Estepona. C. Holotype, MMPE/Ic001.001.001, Velerín, Estepona. D. Paratype, MMPE/Ic001.004.001, Velerín, Estepona. E. Paratype, MMPE/Ic001.005.001, Velerín, Estepona. F. Paratype, JMC−UB/I−0087, Vila−robau, Alt Empordà. G. JMC−UB/I−0130, Rio Torsero, Liguria. H. JMC−UB/I−0089, Vila−robau, Alt Empordà. I. UG−N−P−0117, Almería−Níjar. Scale bars 10 mm.
Fig. 4 in Commensalism in the fossil record: Eunicid polychaete bioerosion on Pliocene solitary corals
Fig. 4. Examples of the three Sulcichnus ichnospecies. Sulcichnus sigillum on Trochocyathus sp. Pairs of pictures correspond to both sides of a single corallite, showing the specular symmetry of the groove. A. Paratype, MMPE/Ic003.002.001, Arroyo Vaquero, Estepona. B. Paratype, MMPE/Ic003.003.001, Velerín, Estepona. C. Holotype, MMPE/Ic003.001.001, Parque Antena, Estepona. S. helicoidalis on Trochocyathus sp. D. Paratype, MMPE/Ic002.002.001, La Lobilla, Estepona. S. helicoidalis on Flabellum sp. E. Holotype, MMPE/Ic002.001.001, Velerín, Estepona. F. Paratype, JMC−UB/I−0086, Vila−robau, Alt Empordà. G. MGSC−3523, Baix Llobregat. H. MGSC−3524, Baix Llobregat. S. maeandriformis on Ceratotrochus sp., Rio Torsero, Liguria. I. MGPUT−I−001. J. MGPUT−I−002. K. MGPUT−I−003. L. MGPUT−I−004. Scale bars 10 mm.
Fig. 2 in Commensalism in the fossil record: Eunicid polychaete bioerosion on Pliocene solitary corals
Fig. 2. Idealized models of Sulcichnus maeandriformis (A), Sulcichnus helicoidalis (B), and Sulcichnus sigillum (C).
FIG. 5. — Leptalpheus felderi n in Description of a new species of commensal alpheid shrimp (Crustacea, Decapoda) from the southern Caribbean Sea
FIG. 5. — Leptalpheus felderi n. sp.: A, B, young ♀ from Colombia (USNM 1022183); A, right major cheliped, distal merus, carpus and chela, mesial view; B, same, fingers slightly opened; C, ♂ paratype from Venezuela (MNHN-Na 13679), telson and uropods, dorsal view. Scale bars: 1 mm.
FIG. 6. — Leptalpheus felderi n in Description of a new species of commensal alpheid shrimp (Crustacea, Decapoda) from the southern Caribbean Sea
FIG. 6. — Leptalpheus felderi n. sp. (A, B) and host Upogebia omissa Gomes Corrêa, 1968 (C), habitus and colour patterns in life: A, ♂ paratype (IVIC 1128), dorsal view; B, ♀ paratype (MNHN-Na 13679), lateral view; C, U. omissa, lateral view.
FIG. 3. — Leptalpheus felderi n in Description of a new species of commensal alpheid shrimp (Crustacea, Decapoda) from the southern Caribbean Sea
FIG. 3. — Leptalpheus felderi n. sp., ♂ paratype (MNHN-Na 13621), right major cheliped (A, B) and left minor cheliped (C-E): A, general view, lateral view; B, fingers of chela opened, mesial view; C, general aspect, lateral view; D, same, ventral view; E, fingers of chela. Scale bars: 1 mm.
FIG. 4. — Leptalpheus felderi n in Description of a new species of commensal alpheid shrimp (Crustacea, Decapoda) from the southern Caribbean Sea
FIG. 4. — Leptalpheus felderi n. sp., ♂ paratype (MNHN-Na 13621): A, third maxilliped, lateral view; B, second pereiopod, lateral view; C, same, distal segment of carpus and chela; D, third pereiopod, lateral view; E, fourth pereiopod, lateral view; F, fifth pereiopod,
FIG. 2. — Leptalpheus felderi n in Description of a new species of commensal alpheid shrimp (Crustacea, Decapoda) from the southern Caribbean Sea
FIG. 2. — Leptalpheus felderi n. sp., ♂ paratype (MNHN-Na 13621), right major cheliped: A, general aspect, ventromesial view; B, chela, mesial view; C, same, ventral view; D, same, lateral view; E, fingers of chela, dorsal view; F, ischium, ventrolateral view; G, distal merus
FIG. 1. — Leptalpheus felderi n in Description of a new species of commensal alpheid shrimp (Crustacea, Decapoda) from the southern Caribbean Sea
FIG. 1. — Leptalpheus felderi n. sp., ♂ paratype (MNHN-Na 13621): A, frontal region, dorsal view; B, same, lateral view; C, carapace, lateral view; D, posterior abdominal segments and tail fan, lateral view; E, antennule, lateral view; F, mandible, incisor process; G, second pleopod. Scale bars: 1 mm.
Figure 5 in Expanding Population Edge Craniometrics and Genetics Provide Insights into Dispersal of Commensal Rats through Nusa Tenggara, Indonesia
Figure 5. Genetic clustering based on allele frequencies of 12 microsatellite loci genotyped for Rattus rattus Complex samples from MSEA and extralimital distribution in Indonesia (IDN). (A) PCoA, (B) STRUCTURE barplot.
Figure 4. Haplotype network for Rattus rattus Complex II in Expanding Population Edge Craniometrics and Genetics Provide Insights into Dispersal of Commensal Rats through Nusa Tenggara, Indonesia
Figure 4. Haplotype network for Rattus rattus Complex II. The Nusa Tenggara samples are illustrated on the right of the network.
Figure 1 in Expanding Population Edge Craniometrics and Genetics Provide Insights into Dispersal of Commensal Rats through Nusa Tenggara, Indonesia
Figure 1. Cranial measurements taken for each specimen: supraoccipital height (BH), basal length (BLL), basilar length (BRL), length of the bullae (BULL), condylobasal length (CBL), condylobasilar length (CBRL), minimum corpus length (CL), length of the diastema (DA), foramen magnum height (FMH), foramen magnum width (FMW), length of the incisive foramina (FOR), length of the face (GES), length of the braincase (HKL), thickness of the incisor (ID), interorbital breadth (IOB), mandibular diastema length (LAL), thickness lower incisor (LID), mandibular alveoli length (MAL), mandibular toothrow length (crown) (MCL),mandibular depth (MD), maximum mandibular height (MDL), mandibular depth at M1 (MID), mandibular length (ML), nasal length (NAS), nasal breadth (NASB), occipital breadth (OCB), occipital length (OCN), supraoccipital width at the occipital condyles (OCW), length of the upper molar row (alveoli) (OZRA), length of the upper molar row (crown) (OZRK), palatal length (PL), palatine breadth (PRL), rostral breadth (RB), rostral height (RH), breadth of braincase (SKB), height of braincase with bullae (SKH), zygomatic plate (ZP), zygomatic breadth (ZYG).
Figure 3. Haplotype networks for Rattus exulans, R in Expanding Population Edge Craniometrics and Genetics Provide Insights into Dispersal of Commensal Rats through Nusa Tenggara, Indonesia
Figure 3. Haplotype networks for Rattus exulans, R. argentiventer, and Rattus rattus Complex LIV. Sunda refers to the islands of Borneo, Java, and Sumatra; the Indonesian sample (brown) lacks further collection information.
Figure 6 in Expanding Population Edge Craniometrics and Genetics Provide Insights into Dispersal of Commensal Rats through Nusa Tenggara, Indonesia
Figure 6. Summary of likely movements of the three commensal rodents through the Nusa Tenggara island chain. Rat illustrations redrawn and adapted from R. Budden, location of RS3 Dong Song drums from Calo (2014).
Data from: Insights into the population genetics of an extreme habitat specialist, the wood ant commensal Formicoxenus nitidulus
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Commensal microbiome dysbiosis in keloid disease
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Urbanization alters the song propagation of two human-commensal songbird species: Active space, amplitude, and attenuation code
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Interspecific coprophagia by wild red foxes: DNA metabarcoding reveals a potentially widespread form of commensalism among animals
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Tissue-resident memory Th17 cells maintain stable fungal commensalism in the oral mucosa
<p>Raw data files linked to a manuscript published in Mucosal Immunology 2020 (accepted for publication on July 6th,.2020)</p>
Commensal bacteria maintain a Qa-1b-restricted unconventional CD8+ T population in gut epithelium
<p>Intestinal intraepithelial lymphocytes (IELs) are characterized by an unusual phenotype and developmental pathway, yet their specific ligands and functions remain largely unknown. Here by analysis of QFL T cells, a population of CD8+ T cells critical for monitoring the MHC I antigen processing pathway, we established that unconventional Qa-1b-restricted CD8+ T cells are abundant in intestinal epithelium. We found that QFL T cells showed a Qa-1b-dependent unconventional phenotype in the spleen and small intestine of naïve wild-type mice. The splenic QFL T cells showed innate-like functionality exemplified by rapid response to cytokines or antigens, while the gut population was refractory to stimuli. Microbiota was required for the maintenance, but not the initial gut homing of QFL T cells. Interestingly, monocolonization with <em>Pediococcus pentosaceus</em>, which expresses a peptide that cross-activated QFL T cells, was sufficient to maintain QFL T cells in the intestine. Thus, microbiota is critical for shaping the Qa-1b-restricted IEL landscape.</p>
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.