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143 results for “invasion success”
Fig. 10 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 10. Trends in the relative abundance of trophic guilds in Lake Fenéki (Piscivores: y = 0.06 + 0.003x; R2 = 0.757; P> 0.00001)
Fig. 9 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 9. Proportion of each species in the cumulative abundance of non-native fish species in Lake Fenéki
Fig. 7 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 7. PCA biplot of the arcsin-square root transformed relative abundance data of the whole sampling period (1992–2011) (Variables: Sampling years; Objects: Relative abundances) (abbreviations were constructed from the Latin names of the species, using the first 3 characters of genus and species
Fig. 5 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 5. Estimated number of species (SD's ignored in order to improve visibility) as a function of number of individuals collected in each sampling year
Fig. 8 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 8. PCA biplot of the arcsin-square root transformed relative abundance data of the period 1994–2011 (Variables: Sampling years; Objects: Relative abundances)
Fig. 4 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 4. Relationships between the age of Lake Fenéki and the Shannon–Weaver index (y = 0.414ln(x) + 0.852; R2 = 0.772; P <0.0001)
Fig. 3 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 3. Relationships between the age of Lake Fenéki and the number of fish species (y = 4.141ln(x) + 3.807; R2 = 0.759; P <0.0001)
Fig. 1 in Long-Term Development Of Fish Assemblage In Lake Fenéki (Kis-Balaton Water Protection System, Hungary): Succession, Invasion And Stabilization
Fig. 1. Overlooking map of the Balaton-catchment, with the sampling site (Dark rectangle marked by the arrow indicates the flooded area of Lake Fenéki)
SBF-SEM datasets related to the manuscript "Trans-cellular tunnels induced by the fungal pathogen Candida albicans facilitate invasion through successive epithelial cells without host damage" by Lachat et al, 2022.
<p>11 serial block face- scanning electron microscopy (SBF-SEM) datasets described in the manuscript "Trans-cellular tunnels induced by the fungal pathogen Candida albicans facilitate invasion through successive epithelial cells without host damage" by Lachat et al, 2022.</p> <p>Resolution: 10 nm x,y, 100 nm Z.</p> <p>Datasets description and quantification can be found in the Supplementary information.</p>
Figure 2 in Reduced genetic diversity and the success of the invasive peacock bass (Cichliformes: Cichlidae)
Figure 2. Gray-greenish and yellowish types of Cichla collected in the reservoirs of the submiddle stretch of São Francisco River.
Invasion success and tolerance to urbanization in birds
<p>Cities are considered hotspot of biological invasions, yet it remains unclear why non-indigenous species are so successful in environments that most local native species do not tolerate. Here, we explore the intriguing possibility that humans may be unintentionally introducing species preadapted to persist in such environments. Combining data on historical introductions with information of avian assemblages along urban-wildland gradients, we found that avian species that in their native range proliferate in human-altered environments have been more likely to be transported and introduced to new locations than species confined to the wildland. We also found that such urban dwellers had higher chances to become established because they already had adaptations to cope with novel environments. These findings suggest that the pathway of introduction selects for species preadapted to persist in novel environments, providing an explanation for why non-indigenous birds are so successful in cities. Because the tendency to introduce species associated with human-altered environments continues, there is an urgent need to develop new regulations to prevent future introductions.</p>
Figure 11 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 11. Hypothetical reconstruction of the jaw adductor musculature in Cymatosaurus sp. A–C, Successively deeper layers of dissection. Abbreviations: amem, m. adductor mandibulae externus medialis; amep, m. adductor mandibulae externus profundus; ames-1b, 1b-portion of m. adductor mandibulae externus superficialis; amp, m. adductor mandibulae posterior; bo.ap, bodenaponeurosis; dm, depressor mandibulae; m.ps, m. pseudotemporalis; m.pt, m. pterygoideus; V2, maxillary branch of trigeminal nerve; V3, mandibular branch of trigeminal nerve.
Figure 4 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 4. Analysis of the jaw mechanics in Placodus on the basis of the model derived by Druzinsky & Greaves (1979). For further discussion see text. Abbreviations: A, B, location of the mandibular joints; E, location of the apex of the coronoid process; bp, bite point in the centre of the posterior dentary tooth plate; F1, f1, resultant vertical muscle force (F1, acting perpendicular to the plane of the drawing) and fulcrum (f1); F2, f2, adductive component of the resultant muscle force generated by posterodorsally inclined muscles (F2, acting perpendicular to the plane of the drawing), and fulcrum (f2)
Figure 3 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 3. Hypothetical reconstruction of the jaw adductor musculature in Placodus gigas. A–D, Successively deeper layers of dissection. Abbreviations: amem, m. adductor mandibulae externus medialis; amep, m. adductor mandibulae externus profundus; ames-1b, 1b-portion of m. adductor mandibulae externus superficialis; amp, m. adductor mandibulae posterior; bo.ap, bodenaponeurosis; dm, depressor mandibulae; m.ps, m. pseudotemporalis; m.pt, m. pterygoideus.
Figure 12 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 12. Hypothetical reconstruction of the jaw adductor musculature in Pistosaurus longaevus. A–C, Successively deeper layers of dissection. Abbreviations: amem, m. adductor mandibulae externus medialis; amep, m. adductor mandibulae externus profundus; ames-1b, 1b-portion of m. adductor mandibulae externus superficialis; amp, m. adductor mandibulae posterior; bo.ap, bodenaponeurosis; dm, depressor mandibulae; m.ps, m. pseudotemporalis; m.pt, m. pterygoideus; V2, maxillary branch of trigeminal nerve; V3, mandibular branch of trigeminal nerve.
Figure 2 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 2. Schematic representation of the trigeminal jaw adductor musculature in extant reptiles (Iguana). A–C, Successively deeper layers of dissection. D, Schematic representation of a horizontal section through the left jaw adductor musculature compelx at the level of the exit of the trigeminal nerve from the braincase. Abbreviations: ame, m. adductor mandibulae externus; amem, m. adductor mandibulae externus medialis; amep, m. adductor mandibulae externus profundus; ames, m. adductor mandibulae externus superficialis; ami, m. adductor mandibulae internus; amp, m. adductor mandibulae posterior; bo.ap, bodenaponeurosis; cid, constrictor internus dorsralis group; lbw, lateral braincase wall; m.ps, m. pseudotemporalis; m.pt, m. pterygoideus; qap, quadrate aponeurosis; uta, upper temporal arch; V1, profundus branch of trigeminal nerve; V2, maxillary branch of trigeminal nerve; V3, mandibular branch of trigeminal nerve.
Figure 9 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 9. Hypothetical reconstruction of the jaw adductor musculature in Nothosaurus mirabilis. A–D, Successively deeper layers of dissection. Abbreviations: amem, m. adductor mandibulae externus medialis; amep, m. adductor mandibulae externus profundus; ames-1b, 1b-portion of m. adductor mandibulae externus superficialis; amp, m. adductor mandibulae posterior; bo.ap, bodenaponeurosis; dm, depressor mandibulae; m.ps, m. pseudotemporalis; m.pt, m. pterygoideus; V2, maxillary branch of trigeminal nerve; V3, mandibular branch of trigeminal nerve.
Figure 10 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 10. Hypothetical reconstruction of the jaw adductor musculature in Corosauruus alcovensis (skull reconstruction after Storrs, 1991 fig. 8). Superficial view of jaw addductor musculature. Abbreviations: amem, m. adductor mandibulae externus medialis; amep, m. adductor mandibulae externus profundus; ames-1b, 1b-portion of m. adductor mandibulae externus superficialis.
Figure 1 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 1. The phylogenetic relationships of Triassic stem-group Sauropterygia (see text, and Rieppel, 2000a for further discussion).
Figure 8 in Feeding mechanics in Triassic stem-group sauropterygians: the anatomy of a successful invasion of Mesozoic seas
Figure 8. Hypothetical reconstruction of the jaw adductor musculature in Simosaurus gaillardoti. A–C, Successively deeper layers of dissection. Abbreviations: amem, m. adductor mandibulae externus medialis; amep, m. adductor mandibulae externus profundus; ames-1b, 1b-portion of m. adductor mandibulae externus superficialis; amp, m. adductor mandibulae posterior; bo.ap, bodenaponeurosis; dm, depressor mandibulae; m.ps, m. pseudotemporalis; m.pt, m. pterygoideus; V2, maxillary branch of trigeminal nerve; V3, mandibular branch of trigeminal nerve.
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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.