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9,937 results for “Endemicity”
Fig 3. A-H in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus
Fig 3. A-H. Trichobothria of left basitibia IV and distitibia IV. A. Charinus brescoviti sp. n. (female holotype, IBSP 149); B. Charinus ricardoi sp. n. (female holotype, MZSP 22036); C. Charinus bonaldoi sp. n. (female paratype, MPEG 0061); D. Charinus guto sp. n. (female holotype, MZSP 48146); E. Charinus carajas sp. n. (female holotype, MZSP 29136); F. Charinus orientalis sp. n. (female paratype, MZSP 29118); G. Charinus ferreus sp. n. (female holotype, MZSP 29104); H. Charinus bichuetteae sp. n. (male paratype, MNRJ 09173). Acronyms: bt, basotibial; bf, basofrontal; bc, basocaudal; sbf, sub-basofrontal; sc, caudal series; sf, frontal series;. Scale bars: 1mm. doi:10.1371/journal.pone.0148277.g003
Fig 2. A-H in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus
Fig 2. A-H. Mesal view of the right chelicerae of all new species here described. A. Charinus brescoviti sp. n. (female paratype, IBSP 149); B. Charinus ricardoi sp. n. (female paratype, MZSP 22036); C. Charinus bonaldoi sp. n. (female paratype, MPEG 0061); D. Charinus guto sp. n. (female paratype, MZSP 41460); E. Charinus carajas sp. n. (male paratype, MZSP 28291); F. Charinus orientalis sp. n. (female paratype, MZSP 29118); G. Charinus ferreus sp. n. (female paratype, MZSP 29106); H. Charinus bichuetteae sp. n. (male paratype, MNRJ 9173). Scale bars: 1mm. doi:10.1371/journal.pone.0148277.g002
Fig 1. A-E in Eight New Species of Charinus Simon, 1892 (Arαchnidα: Amblypygi: Chαrinidαe) Endemic for the Brαziliαn Amαzon, with Notes on Their Conservαtionαl Stαtus
Fig 1. A-E. Habitus and details of the sternum and pedipalp of Charinus brescoviti sp. n. (female, MNRJ 9186). A. Dorsal habitus; B. Sternum; C. Frontal view of left the pedipalp basitiba, distitiba and claw; D. Dorsal view of the right pedipalp; E. Ventral view of the left pedipalp. Scale bars: 1mm. doi:10.1371/journal.pone.0148277.g001
Fig 3 in Ptilagrostis contracta (Stipeae, Poaceae), a New Species Endemic to Qinghai-Tibet Plateau
Fig 3. Illustration of Ptilagrostis contracta. A. habit; B. glume; C. floret; D. palea; E. callus F. outer surface of ligule; G. inner surface of ligule. Scale bar in B, C, F, G represent 5 mm; in D represent 2 mm; in E represent 0.5 mm (Drawn by Z. S. Zhang). doi:10.1371/journal.pone.0166603.g003
Fig. 6 in Ecophysiological responses to the effect of annual management on an endemic viviparous fish in central plateau of México
Fig. 6. Bimonthly structure of the population of G. multiradiatus in San Martin. Shows the curves of growth with the von Bertalanffy model for highly seasonal cycles. Upon reaching the asymptotic curve determines the final class of each age cohort.
Fig. 5 in Ecophysiological responses to the effect of annual management on an endemic viviparous fish in central plateau of México
Fig. 5. General structure of the population of San Martín mexcalpique. The numbers in parentheses indicate the percentage of each size class of the total population.
Fig. 8 in Ecophysiological responses to the effect of annual management on an endemic viviparous fish in central plateau of México
Fig. 8. Percentages of each food components found in the digestive tract of G. multiradiatus during a hydrological cycle in san Martín dam.
Fig. 4 in Ecophysiological responses to the effect of annual management on an endemic viviparous fish in central plateau of México
Fig. 4. Number of individuals (bars) and mean biomass of the population (line curve) of mexcalpiques during a hydrological cycle.
Fig. 2 in Ecophysiological responses to the effect of annual management on an endemic viviparous fish in central plateau of México
Fig. 2. Ombrothermic diagram for San Martin dam, Amealco, Qro. It shows hydrological periods of importance to the life cycle of mexcalpique.
Figure 1 in New records and updated distribution of the endemic Balkan rock lizards Dinarolacerta spp. in Montenegro
Figure 1. Updated distribution of D. mosorensis (circles) and D. montenegrina (triangles) in Montenegro (locality numbers explained in Appendix I). Solid symbols – new records; open symbols - literature data.
Figure 6 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.
Figure 6. – Dorsal fin on a live paratype of Thymallus ligericus n. sp. MNHN 2018-0726, 290 mm SL ♀, Lignon River at Boën-surLignon, 29 May 2015, Persat, Juglaret and Buttazzoni coll.
Figure 4 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.
Figure 4. – Mouth in ventral view of Thymallus spp. A: Holotype of Thymallus ligericus n. sp. MNHN 2018-0722, 337 mm SL J, Alagnon River at La Chapelle d'Alagnon, 9 Sep. 2016, Persat and FDAAPPMA15 coll.; B: Thymallus thymallus UCBLZ 2012.9.1010, 376 mm TL, Rhône drainage, Ain River at Crotenay, 10 Jun. 2014, Persat and FDAAPPMA39 coll.
Figure 2 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.
Figure 2. – Specimens of Thymallus spp. in lateral view. Holotype of Thymallus ligericus n. sp. MNHN 2018- 0722, 337 mm SL J, Alagnon River at La Chapelle d'Alagnon, 9 Sep. 2016, Persat and FDAAPPMA 15 coll., in live (A) and after preservation (B); Paratype of Thymallus ligericus n. sp. MNHN 2019-0267 (C), 269 mm SL ♀, Loire River at Chadron, 22 Sep. 2016, Persat and ONEMA43 coll; UCBLZ – 2012.9.1011 (D), 292 mm TL, Rhône drainage, Ain River at Crotenay, 10 Jun. 2014, Persat and FDAAPPMA39 coll.
Figure 1 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.
Figure 1. – The three supplementary measurements made on the ventral side of the head, in addition to those of Surre et al. (1986): the mandible width, the chin length (from the basibranchial junction to the extremity of the mandible) and the ventral snout length (from the same point to the extremity of the snout).
Figure 3 in A third European species of grayling (Actinopterygii, Salmonidae), endemic to the Loire River basin (France), Thymallus ligericus n. sp.
Figure 3. – Head profiles of Thymallus spp. A: Paratype of Thymallus ligericus n. sp. MNHN 2018-0728, 300 mm SL J, Dore River at Vertolaye, 29 May 2015, Persat, Juglaret and Buttazzoni coll.; B: Thymallus thymallus UCBLZ – 2012.9.1010, 376 mm TL, Rhône drainage, Ain River at Crotenay, 10 Jun. 2014, Persat and FDAAPPMA39 coll.
FIGURE 2. 3D in The inner morphology of the petrosal bone of the endemic elephant of Tilos Island, Greece
FIGURE 2. 3D reconstruction of the petrosals, samples (A-C) T2406 along with transparent views locating the orientation of the labyrinth in the bone, (D-F) T2506 and (G-I) T137. A, D, G ventrolateral view; B, E, H dorsolateral view; C, F, I dorsomedial view. See text for abbreviations.
Figure 5 in Barbatula leoparda (Actinopterygii, Nemacheilidae), a new endemic species of stone loach of French Catalonia
Figure 5. – Distribution map of the three recognized Barbatula spp. in France and Spain adapted and modified from Kottelat and Freyhof (2007): Barbatula leoparda in yellow, Barbatula barbatula in blue and Barbatula quignardi in orange. Locations: Têt River at Nefiach (1), Tech River at Céret (2) and at Elne (3).
Figure 2 in Barbatula leoparda (Actinopterygii, Nemacheilidae), a new endemic species of stone loach of French Catalonia
Figure 2. – Specimens of Barbatula spp. in ventral view. A: Holotype of Barbatula leoparda MNHN 2018- 0228, 62.6 mm SL ♀, Têt River at Nefiach, 7 Sep. 2016, Denys and ONEMA coll.; B: Barbatula barbatula MNHN 2013-0826, 72.9 mm SL ♂, stream Clauge (Rhône drainage) at La Loye, 1 Jul. 2013, Denys and ONEMA coll.; C: Holotype of Barbatula quignardi MGAB77, 52 mm SL ♂, Lez River, Jul. 1962, Băcescu coll.
Fig. 1. Vriesea incurvata plantlets after 180 in In vitro propagation of Vriesea incurvata: conservation of a bromeliad endemic to the Atlantic Forest
Fig. 1. Vriesea incurvata plantlets after 180 days in MS medium with different macronutrient combinations (25N and 25M) and sucrose concentrations (10, 30 and 60 g L-1). 25M - 25% of the original concentrations of the macronutrients; 25N - 25% of the original concentrations of the nitrogenous salts. Scale bars = 1 cm.
Fig. 2. Area diagram depicting relationships among the 24 in Biogeography of freshwater fishes from the Northeastern Mata Atlântica freshwater ecoregion: distribution, endemism, and area relationships
Fig. 2. Area diagram depicting relationships among the 24 coastal drainages analyzed, obtained by parsimony analysis of endemicity based on freshwater fishes. The topology represents the strict consensus of five equally parsimonious trees obtained through a heuristic search (length= 71 steps, CI = 0.521, RI = 0.709).
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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.