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592 results for “forest distributions”
Fig. 2 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 2. Lateral view of head, left side, showing the snout profile of Scleromystax reisi, holotype, MCP 49070, 49.3 mm SL (a), and S. salmacis, holotype, MCP 38388, 36.7 mm SL (b; modified from Britto & Reis, 2005: fig. 1).
Fig. 6 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 6. Scleromystax reisi, paratype, female, UFRGS 19189, 46.1 mm SL, Estação Experimental Agronômica, Universidade Federal do Rio Grande do Sul, Eldorado do Sul, RS, Brazil.
Fig. 1 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 1. Scleromystax reisi, holotype, male, MCP 49070, 49.3 mm SL, arroio Demétrio, Morungava, Gravataí, RS, Brazil.
Fig. 5 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 5. Right pectoral spine of Scleromystax reisi, paratype, male, MNRJ 43857. Small, whiskerlike odontodes removed. Scale bar: 1.0 mm.
Fig. 8 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 8. Map of northern Rio Grande do Sul State and southern Santa Catarina State, Brazil, showing the distribution of Scleromystax reisi in the laguna dos Patos drainage (yellow symbols; star = type locality) and the distribution of S. salmacis (red symbols; triangle = first record to the rio Tramandaí drainage).
Fig. 4 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 4. Infraorbital series and adjacent cranial bones, lateral view, of: Scleromystax reisi, paratype, MNRJ 43857 (largest image, left side); a. S. salmacis, MCP 28729 (right side, flipped horizontally); b. S. macropterus, UFRJ 4442 (left side); c. S. prionotos, UFRJ 4428 (right side, flipped horizontally); d. S. barbatus, UFRJ 4440 (right side, flipped horizontally). Arrowheads showing ventral expansion of infraorbital 2. Solid lines detaching ventral margin of infraorbital 2 and bone sutures. Eye removed from specimens in a-d. Scale bar: 1.0 mm.
Fig. 3 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 3. Detail of dorsal view of cranium of Scleromystax reisi, paratype, female, MNRJ 43857 (top), and S. salmacis, male, MCP 28729 (bottom; flipped horizontally, left infraorbitals and suspensorium removed). Solid lines detaching limits of bone sutures. Scale bar: 1.0 mm.
Fig. 7 in New species of Scleromystax Günther, 1864 (Siluriformes: Callichthyidae) - extending the meridional distribution of genera endemic to the Atlantic Forest
Fig. 7. Scleromystax reisi, paratypes. Changes in the color pattern during early stages of the ontogenesis. MCP 48177, 13.5 mm SL (top); MCP 48178, 18.8 mm SL (middle); UFRGS 19191, 19.4 mm SL (bottom).
Figure 2 in Forest monkeys and Pleistocene refugia: a phylogeographic window onto the disjunct distribution of the Chlorocebus lhoesti species group
Figure 2. All possible patterns of relationships among the lhoesti group species. A, topology consistent with a vicariant scenario in which the distribution of a widespread common ancestor fragments into three segments – nearly simultaneously – as the result of habitat deterioration associated with a Pleistocene glacial cycle. B, topology consistent with an alternative vicariant scenario, in which ancestral populations of Chlorocebus preussi and Chlorocebus solatus remain in contact for a short time after the divergence of Chlorocebus lhoesti, because the former two stocks range within the same Pleistocene refuge. C, tree consistent with a dispersal hypothesis in which early C. preussi populations (following divergence from C. solatus) migrate along the northern rim of the Congo Basin, and found a new lineage (C. lhoesti) in the Albertine region (see Fig. 1). D, tree consistent with a dispersal hypothesis in which early C. solatus populations (following divergence from C. preussi) conduct a similar transcontinental migration, but along the southern rim of the Congo Basin (see Fig. 1).
Рис. 1. Карта района иссΛеΑований. 1 – граница зон раститеΛьности; 2 – граница поΑзон раститеΛьности; 3 – места сбора материаΛа; I – южная тайга; II – среΑняя тайга; III – северная тайга; IV – крайнесеверная тайга; V – ΛесотунΑра; VI – южная тунΑра; VII – северная тунΑра. Fig. 1. Map of the studied area. 1 – boundary of vegetation zones; 2 – boundary of vegetation subzones; 3 – collection points; I – southern taiga; II – middle taiga; III – northern taiga; IV – extremely northern taiga; V – forest tundra; VI – southern tundra; VII – northern tundra. in Fauna and landscape-zonal distribution of Orthoptera in the Komi Republic (Russia)
Рис. 1. Карта района иссΛеΑований. 1 – граница зон раститеΛьности; 2 – граница поΑзон раститеΛьности; 3 – места сбора материаΛа; I – южная тайга; II – среΑняя тайга; III – северная тайга; IV – крайнесеверная тайга; V – ΛесотунΑра; VI – южная тунΑра; VII – северная тунΑра. Fig. 1. Map of the studied area. 1 – boundary of vegetation zones; 2 – boundary of vegetation subzones; 3 – collection points; I – southern taiga; II – middle taiga; III – northern taiga; IV – extremely northern taiga; V – forest tundra; VI – southern tundra; VII – northern tundra.
Original data for the paper "Ericaceous dwarf shrubs in drained forested peatlands: distribution, dynamics and key factors in a restoration experiment"
Open the record for dataset details and reuse information.
Text-fig. 1. Context and location of the Govone outcrop. a: Location of the Piedmont Basin at the northern margin of the Mediterranean Basin and distribution of Messinian evaporites. b: Simplified geological map of the Piedmont Basin showing the location of the Govone outcrop close to the town of Alba. in Remains Of A Subtropical Humid Forest In A Messinian Evaporitebearing Succession At Govone, Northwestern Italy - Preliminary Results
Text-fig. 1. Context and location of the Govone outcrop. a: Location of the Piedmont Basin at the northern margin of the Mediterranean Basin and distribution of Messinian evaporites. b: Simplified geological map of the Piedmont Basin showing the location of the Govone outcrop close to the town of Alba.
Figure 3 in Woody species distribution across a savanna-dry forest soil gradient in the Brazilian Cerrado
Figure 3. Proportional occurrence of 51 woody species across 30 plots ordinated by the soil gradient of aluminum saturation and base saturation (RDA axis 1, see Figure 1) in a savanna-dry forest transition. Grey and black bars correspond to cerrado stricto sensu and dry forest plots, respectively.
Figure 2 in Woody species distribution across a savanna-dry forest soil gradient in the Brazilian Cerrado
Figure 2. Topography and the gradients of aluminum saturation, base saturation, and phosphorus across 30 plots (rectangles, 10×40 m) in a 4.5 ha area of contact between the cerrado stricto sensu (SA) and dry forest (DF) physiognomies.
Figure 1 in Woody species distribution across a savanna-dry forest soil gradient in the Brazilian Cerrado
Figure 1. Biplot of tb-RDA for woody species composition, and relationships with edaphic (P = phosphorous; A = aluminum saturation; B = base saturation) and spatial (M1 and M2) variables, among plots in cerrado stricto sensu (gray) or dry forest (black) physiognomies.
Fig. 2 in Spatial Distribution Of Nematodes In The Forest Ecosystem Of The Mezin National Nature Park, Ukraine
Fig. 2. Abundance of nematodes belonging to different orders in the studied microhabitats of forest ecosystem.
Fig. 1 in Spatial Distribution Of Nematodes In The Forest Ecosystem Of The Mezin National Nature Park, Ukraine
Fig. 1. Species diversity of nematodes belonging to different orders in the studied microhabitats of forest ecosystem.
Fig. 3 in Spatial Distribution Of Nematodes In The Forest Ecosystem Of The Mezin National Nature Park, Ukraine
Fig. 3. Structure of nematode fauna of the studied microhabitats of forest ecosystem according to the dominance criterion: A — species diversity, %; B — abundance, %.
Fig.3 in Biodiversity survey, ecology and new distribution records of Marchantiophyta in a remnant of Brazilian Atlantic Forest
Fig.3. Graphical representation of substrates colonized by liverwort species in the fragment of dense montane ombrophilous forest studied in the National Park of Boa Nova, Bahia, Brazil.
gellum black. Femora all black or forefemur ferruginous in apicoventral half; foretibia brown or ferruginous, midtibia brown ferruginous, hindtibia brown; tarsi varying from brown to ferruginous. ♂.– Unknown. GEOGRAPHIC DISTRIBUTION.– Known only from higher elevations (1020-1130 m above sea level) of Ranomafana National Park, Madagascar. RECORDS (Fig. 29).— All specimens were collected in Ranomafana National Park, Fianarantsoa Province. Holotype: ♀, Belle Vue at Talatakely at 21º15.99'S 47º25.21'E, alt. 1020 m, 14-21 Jan 2002, M. Irwin and R. Harin 'Hala (CAS). Paratypes: Radio tower at forest edge at 21º15.05'S 47º24.43'E, alt. 1130 m, 23 Aug – 7 Sept 2006 and 1-11 Nov 2006, M. Irwin and R. Harin 'Hala (2 ♀, CAS); same data as holotype except 22-28 Nov 2001 and R. Harin 'Hala alone (1 ♀, CAS); Vohiparara at 21º13.57'S 47º22.19'E, alt. 1110 m, 22-28 Nov 2001, R. Harin 'Hala (1 ♀, CAS). FIGURE 29. Collecting localities of Tachytes melanogaster sp. nov. in A Review of the Wasp Genus Tachytes Panzer, 1806 of Madagascar (Hymenoptera: Crabronidae)
gellum black. Femora all black or forefemur ferruginous in apicoventral half; foretibia brown or ferruginous, midtibia brown ferruginous, hindtibia brown; tarsi varying from brown to ferruginous. ♂.– Unknown. GEOGRAPHIC DISTRIBUTION.– Known only from higher elevations (1020-1130 m above sea level) of Ranomafana National Park, Madagascar. RECORDS (Fig. 29).— All specimens were collected in Ranomafana National Park, Fianarantsoa Province. Holotype: ♀, Belle Vue at Talatakely at 21º15.99'S 47º25.21'E, alt. 1020 m, 14-21 Jan 2002, M. Irwin and R. Harin 'Hala (CAS). Paratypes: Radio tower at forest edge at 21º15.05'S 47º24.43'E, alt. 1130 m, 23 Aug – 7 Sept 2006 and 1-11 Nov 2006, M. Irwin and R. Harin 'Hala (2 ♀, CAS); same data as holotype except 22-28 Nov 2001 and R. Harin 'Hala alone (1 ♀, CAS); Vohiparara at 21º13.57'S 47º22.19'E, alt. 1110 m, 22-28 Nov 2001, R. Harin 'Hala (1 ♀, CAS). FIGURE 29. Collecting localities of Tachytes melanogaster sp. nov.
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Allen Brain Atlas
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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
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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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