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760 results for “Species occurrences”
Fig. 2 in Notes on the occurrence of Acetropis Fieber, 1858 (Hemiptera: Heteroptera: Miridae) in Poland, with a key to Polish species
Fig. 2. Distribution of A. carinata in western Palaearctic (orig.)
Data from: The relationship between native species richness and exotic species richness or occurrence will always be negative when the total number of species is accounted for in statistical models: A response to Beaury et al.
Beaury et al. (2020) attempt to address the scale dependence of evidence for biotic resistance by including environmental covariates that can account for total species richness. However, this approach will incorrectly estimate relationships, driven by the accuracy of the covariates rather than the true relationship between native and non-native species.
Supplementary material 1 from: Seebens H, Kaplan E (2022) DASCO: A workflow to downscale alien species checklists using occurrence records and to re-allocate species distributions across realms. NeoBiota 74: 75-91. https://doi.org/10.3897/neobiota.74.81082
Manual of DASCO
Environmental variables and occurrence of 13 fish species
<p>Species-environment relationships were studied between the occurrence of 13 fish and lamprey species and 9 mainly map-based environmental variables of Finnish boreal small streams. A self-organizing map (SOM) analysis showed strong relationships between the fish species and environmental variables in a single model (explained variance 55.9%). Besides basic environmental variables such as altitude, catchment size, and mean temperature, landcover variables were also explored. A logistic regression analysis indicated that the occurrence probability of brown trout, <i>Salmo trutta</i> L., decreased with an increasing percentage of peatland ditch drainage in the upper catchment. Ninespine stickleback, <i>Pungitius pungitius </i>(L.), and three-spined stickleback, <i>Gasterosteus aculeatus </i>L., seemed to benefit from urban areas in the upper catchment. Discovered relationships between fish species occurrence and land-use attributes are encouraging for the development of fish-based bioassessment for small streams. The presented ordination of the fish species in the mean temperature gradient will help in predicting fish community responses to climate change.</p>
Figure 2 from: Guillaumot C, Martin A, Fabri-Ruiz S, Eléaume M, Saucède T (2016) Echinoids of the Kerguelen Plateau – occurrence data and environmental setting for past, present, and future species distribution modelling. ZooKeys 630: 1-17. https://doi.org/10.3897/zookeys.630.9856
Figure 2 - Distribution of the 12 echinoid species based on the specimens collected since 1872 on the Kerguelen Plateau.
Figure 1 from: Guillaumot C, Martin A, Fabri-Ruiz S, Eléaume M, Saucède T (2016) Echinoids of the Kerguelen Plateau – occurrence data and environmental setting for past, present, and future species distribution modelling. ZooKeys 630: 1-17. https://doi.org/10.3897/zookeys.630.9856
Figure 1 - Sampling effort. Red dots depict echinoid occurrences. Black squares correspond to visited sites at which no echinoid was sampled.
Figures 9–15 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 9–15: Parabuthus eritreaensis, female. Figure 9. Carapace and tergites I–IV. Figures 10–11. Sternopectinal area and sternites.. Figures 12–15. Right legs I–IV, retrolateral aspect.
Figures 36–48 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 36–48: Parabuthus dorisae sp. n., male holotype. Figures 36–46. Right pedipalp, chela in dorsal (36), external (37), and ventral (38) views, patella in dorsal (39), external (40), and ventral (41) views, femur and trochanter in internal (42), dorsal (43), and ventral (44) views. Dentate margins of movable (45) and fixed (46) fingers. Trichobothrial pattern indicated in Figures 37– 40 and 42–43 by white circles. Figure 47. Carapace and tergites I–V. Figures 48. Sternopectinal area and sternites.
Figures 94–95 in Scorpions of the Horn of Africa (Arachnida: Scorpiones). Part XXX. Parabuthus (Buthidae) (Part III), with description of three new species from Somaliland and occurrence of Parabuthus eritreaensis Kovařík, 2003
Figures 94–95: Parabuthus quincyae sp. n., male holotype. Figure 94. Male holotype in vivo habitus. Figure 95. Locality, Somaliland, vicinity of Huluul.
FIGURE 11 in On the Albian occurrence of Armigatus (Teleostei, Clupeomorpha) in America, a new species from the Tlayúa Lagerstätte, Mexico
FIGURE 11. Phylogenetic hypotheses of Ellimmichthyiformes that show the different positions of Armigatus (dark lines) and members of this order (dark circle) and Clupeiformes (white square).
FIGURE 1. Specimen IGM 11532 in On the Albian occurrence of Armigatus (Teleostei, Clupeomorpha) in America, a new species from the Tlayúa Lagerstätte, Mexico
FIGURE 1. Specimen IGM 11532, Armigatus brevissimus from the Cenomanian shallow marine deposits of Hekel, Lebanon, coated with magnesium smoke.
FIGURE 4 in On the Albian occurrence of Armigatus (Teleostei, Clupeomorpha) in America, a new species from the Tlayúa Lagerstätte, Mexico
FIGURE 4. Paratypes of Armigatus carrenoae sp. nov. from Albian deposits of Tlayúa lagerstätte, near Tepexi de Rodríguez, Puebla, Mexico, photographed under UV light. A, IGM 11537. B, IGM 11538. C, IGM 11540.
FIGURE 5 in On the Albian occurrence of Armigatus (Teleostei, Clupeomorpha) in America, a new species from the Tlayúa Lagerstätte, Mexico
FIGURE 5. Head of Armigatus carrenoae sp. nov. from the Albian deposits of Tlayúa lagerstätte, near Tepexi de Rodríguez, Puebla, Mexico. A, Closeup of IGM 11538, coated with magnesium smoke and photographed under white light. B, idealized and simplified drawing of A. Abbreviations: aa, anguloarticular; ao, antorbital; br, branchiostegal ray; cl, cleithrum; ddml depression for the dento-maxillar ligament; den, dentary; dsph, dermosphenotic; ect, ectopterygoid; ent, endopterygoid; epo, epioccipital; epn, epineurals; ext, extrascapular; fr, frontal; hm, hyomandibular; io, infraorbital; iop, interopercle; le, lateral ethmoid; mes, mesethmoid; mp, metapterygoid; mx, maxilla; na, nasal; naac, neural arches + spines of abdominal centrum; op, opercle; os, orbitosphenoid; os, orbitosphenoid; pa, parietal; pal, palatine; pcl, postcleithrum; pd, predorsal; pfr, pectoral fin ray; pop, preopercle; prvas, prepelvic abdominal scutes; psp, parasphenoid; pto, pterotic; pts, pterosphenoid; ptt, posttemporal; q, quadrate; r, rib; rar, retroarticular; sc, sclerotic; scl, supracleithrum; smx, supramaxilla; soc, supraoccipital; sop, subopercle; suo, supraorbital; dark arrow shows the basipterygoid process of the parasphenoid bone; (l) and (r) indicates the left and right side.
FIGURE 3. IGM 11536 in On the Albian occurrence of Armigatus (Teleostei, Clupeomorpha) in America, a new species from the Tlayúa Lagerstätte, Mexico
FIGURE 3. IGM 11536, holotype of Armigatus carrenoae sp. nov. from the Albian deposits of Tlayúa lagerstätte, near Tepexi de Rodríguez, Puebla, Mexico. A, photograph of the complete specimen under UV light. B, idealized drawing of the same specimen.
Occurrence data for 18 tree species used in a common garden experiment
<p>Occurance data for 18 tropical rainforest tree species from across their home range downloaded from gbif, processed and used in the determination of ecoclimatic niche maps as part of work examinnig variation in growth and survival when grown under contrasting common garden sites</p>
Figure 7 from: Liu W, Golovatch S (2018) Occurrence of the millipede genus Tonkinosoma Jeekel, 1953 in China, with the description of the first presumed troglobitic species of this genus (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 742: 23-34. https://doi.org/10.3897/zookeys.742.23471
Figure 7 Tonkinosoma tiani sp. n., ♂ paratype from Ganhan Cave. A–C left gonopod, mesal, anterior and lateral views, respectively. Abbreviations: fe = femorite; ll = lamella lateralis; lm = lamella medialis; pf = postfemur; s = sulcus; sg = seminal groove; sl = solenomere; sph = solenophore; t = tooth.
Figure 8 from: Liu W, Golovatch S (2018) Occurrence of the millipede genus Tonkinosoma Jeekel, 1953 in China, with the description of the first presumed troglobitic species of this genus (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 742: 23-34. https://doi.org/10.3897/zookeys.742.23471
Figure 8 Tonkinosoma tiani sp. n., ♂ paratype from Ganhan Cave. A, B left gonopod, submesal and lateral views, respectively. Abbreviations: s = sulcus; sl = solenomere; sph = solenophore; t = tooth.
Figure 5 from: Liu W, Golovatch S (2018) Occurrence of the millipede genus Tonkinosoma Jeekel, 1953 in China, with the description of the first presumed troglobitic species of this genus (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 742: 23-34. https://doi.org/10.3897/zookeys.742.23471
Figure 5 Tonkinosoma tiani sp. n., ♂ paratype from Ganhan Cave. A–C anterior part of body, dorsal, ventral and lateral views, respectively D–F midbody segments; dorsal, ventral and lateral views, respectively G–I posterior part of body, dorsal, ventral and lateral views, respectively. Scale bar: 0.2 mm.
Figure 3 from: Liu W, Golovatch S (2018) Occurrence of the millipede genus Tonkinosoma Jeekel, 1953 in China, with the description of the first presumed troglobitic species of this genus (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 742: 23-34. https://doi.org/10.3897/zookeys.742.23471
Figure 3 Tonkinosoma flexipes Jeekel, 1953, ♂. A, B right gonopod, lateral and mesal views, respectively. Abbreviations: fe = femorite; ll = lamella lateralis; lm = lamella medialis; pf = postfemur; sg = seminal groove; sl = solenomere.
Figure 6 from: Liu W, Golovatch S (2018) Occurrence of the millipede genus Tonkinosoma Jeekel, 1953 in China, with the description of the first presumed troglobitic species of this genus (Diplopoda, Polydesmida, Paradoxosomatidae). ZooKeys 742: 23-34. https://doi.org/10.3897/zookeys.742.23471
Figure 6 Tonkinosoma tiani sp. n., ♂ paratype from Ganhan Cave. A, B segments 6–8, dorsal and lateral views, respectively C sternite V, ventral view D gonopods in situ, ventral view E legs 4 and 9, anterior view. Abbreviations: b = tarsal brush; o = ozopore; pl = pleurosternal carina.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.