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9,937 results for “Endemicity”
Figure 3. Cotylopus rubripinnis n in The genus Cotylopus (Teleostei: Gobioidei) endemic to the rivers of islands of the Indian Ocean with description of a new species from Mayotte (Comoros)
Figure 3. Cotylopus rubripinnis n. sp., MNHN 2004-0561 (live specimen), Koualé river, Mayotte, 3 November 2003, G. Marquet, P. Valade, E. Feunteun, P. Bosc, and T. Hoareau coll. (photograph: P. Bosc).
Figure 2 in The genus Cotylopus (Teleostei: Gobioidei) endemic to the rivers of islands of the Indian Ocean with description of a new species from Mayotte (Comoros)
Figure 2. Diagrammatic illustration of urogenital papilla in Cotylopus rubripinnis. (a) Male; (b) female. 1, Anus; 2, urogenital papilla; 3, anal fin.
Figure 1 in The genus Cotylopus (Teleostei: Gobioidei) endemic to the rivers of islands of the Indian Ocean with description of a new species from Mayotte (Comoros)
Figure 1. Diagrammatic illustration of head in Cotylopus rubripinnis. (a) Dorsal view; (b) lateral view; (c) ventral view.
Figure 4 in Revision of the southern South American endemic genus Anomiopsoides Blackwelder, 1944 (Coleoptera: Scarabaeidae: Scarabaeinae: Eucraniini) and description of its food relocation behavior
Figure 4. Distributional map of Anomiopsoides aurita (Burmeister), A. biloba (Burmeister), and A. catamarcae Martínez.
Figure 3 in Revision of the southern South American endemic genus Anomiopsoides Blackwelder, 1944 (Coleoptera: Scarabaeidae: Scarabaeinae: Eucraniini) and description of its food relocation behavior
Figure 3. Mesotibial apex and external tibial spur of: (a) Anomiopsoides biloba (Burmeister); (b) A. catamarcae Martínez.
Figure 2 in Revision of the southern South American endemic genus Anomiopsoides Blackwelder, 1944 (Coleoptera: Scarabaeidae: Scarabaeinae: Eucraniini) and description of its food relocation behavior
Figure 2. Dorsal view of the head of: (a) Anomiopsoides aurita (Burmeister); (b) A. catamarcae Martínez; (c, d) A. cavifrons (Burmeister), male and female, respectively; (e) A. biloba (Burmeister); (f, g) A. heteroclyta (Bermeister), male and female, respectively.
Figure 4 in Ecologically-sustainable tree monocultures contribute to conservation of an Araucaria Forest endemic frog
Figure 4. Mean (¡SE) number of food items per stomach in each habitat. FO, Araucaria Forest; PA, Araucaria angustifolia plantation; PP, Pinus plantation; PE, Eucalyptus plantation.
Figure 5 in Ecologically-sustainable tree monocultures contribute to conservation of an Araucaria Forest endemic frog
Figure 5. Rarefaction curves of Physalaemus lisei diet, relating taxonomic richness to the number of individuals in each habitat. FO, Araucaria Forest; PA, Araucaria angustifolia plantation; PP, Pinus plantation; PE, Eucalyptus plantation. The vertical lines comprise the 95% confidence intervals.
Figure 3 in Ecologically-sustainable tree monocultures contribute to conservation of an Araucaria Forest endemic frog
Figure 3. Diet composition of Physalaemus lisei (black bars) in relation to the taxonomic composition of pitfall traps (white bars). Dotted line delimits the feeding niche of P. lisei.
Figure 2 in Ecologically-sustainable tree monocultures contribute to conservation of an Araucaria Forest endemic frog
Figure 2. Body mass (g) distribution of Physalaemus lisei captured in the São Francisco de Paula National Forest, southern Brazil. (A) Temporal variation in body mass (g) distribution between October 2003 and April 2005; (B) among-habitat variation in body mass distribution. Horizontal line represents the median; the box delimits the first and third quartile; the vertical lines delimit the maximum and minimum values, except for the outliers that are represented by asterisks. FO, Araucaria Forest; PA, Araucaria angustifolia plantation; PP, Pinus plantation; PE, Eucalyptus plantation.
Figure 1 in Ecologically-sustainable tree monocultures contribute to conservation of an Araucaria Forest endemic frog
Figure 1. Number of individuals of Physalaemus lisei captured in the São Francisco de Paula National Forest, southern Brazil. (A) Temporal dynamic between October 2003 and April 2005; (B) among-habitat variation in the mean (¡SE) number of captures. FO, Araucaria Forest; PA, Araucaria angustifolia plantation; PP, Pinus plantation; PE, Eucalyptus plantation.
Figure 1 in Trichodina modesta Lom, 1970 (Ciliophora: Peritrichia) infestations of an endemic Toothcarp Aphanius danfordii Boulenger, 1890 (Pisces: Cyprinodontidae) in Sinop, Turkey
Figure 1. (A) Diagrammatic drawings of the denticles of Trichodina modesta; (B) a silver nitrate-stained specimen of T. modesta. Scale bar: 10 Mm.
Figure 49 in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 49. Shell size ranges of Amplirhagada species described herein. Box plot diagrams showing the median (line in box), the 25% (box) and 75% percentile (lines outside box) and extremes (asterisks) of shell height (above) and shell width (below) of species sorted by their height. Species numbers refer to the manuscript names of the described species as used by Solem (1991): 27, A. coffea. 29, A. lindsayae. 22, A. vialae. 26, A. inusitata. 19, A. alicunda. 31, A. bendraytoni. 28, A. gardneriana. 35, A. epiphallica. 21, A. davidsoniana. 24, A. discoidea. 17, A. atlantis. 33, A. angustocauda. 25, A. forrestiana. 20, A. moraniana. 36, A. carinata. 18, A. carsoniana.
Figure 48 in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 48. Penial anatomy of Amplirhagada carinata Solem, 1981. (A) Interior anatomy of the penial wall (WAM S34759). (B) Interior anatomy of the penial wall (WAM S34763). For labelling of structures see Fig. 4. Scale bars = 3 mm.
Figure 46. Amplirhagada carinata Solem, 1981 in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 46. Amplirhagada carinata Solem, 1981 SEM of shell, radula and jaw (WAM S34759). (A) Protoconch and first teleoconch whorls viewed from above. (B) Detail of first teleoconch whorls viewed from above. (C) Close-up of sculpture on last whorl, lateral view. (D) Jaw. (E) Central and inner lateral teeth viewed from above. (F) Marginal teeth viewed from above. Scale bars: A–C, 200 µm; D, 100 µm; E–F, 10 µm.
Figure 45 in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 45. Penial anatomy of Amplirhagada epiphallica n.sp. (WAM S34746). For labelling of structures see Fig. 4. (A) Interior anatomy of the penial wall. (B) Schematic view of the penis with the penial sheath being removed. Scale bars = 5 mm.
Figure 43. Amplirhagada epiphallica n in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 43. Amplirhagada epiphallica n.sp. SEM of shell, radula and jaw (WAM S34746). (A) Protoconch and first teleoconch whorls viewed from above. (B) Detail of first teleoconch whorls viewed from above. (C) Close-up of sculpture on last whorl, lateral view. (D) Jaw. (E) Central and inner lateral teeth viewed from above. (F) Marginal teeth viewed from above. Scale bars: A–C, 1 mm; D, 100 µm; E–F, 10 µm.
Figure 39 in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 39. Penial anatomy of Amplirhagada bendraytoni n.sp. (WAM S34741). For labelling of structures see Fig. 4. (A) Schematic view of the penis with the penial sheath being removed. Scale bar = 5 mm. (B) Interior anatomy of the penial wall. Scale bar = 5 mm. (C) Schematic cross-section of the main pilaster (not to scale).
Figure 41 in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 41. Genitalia of Amplirhagada angustocauda n.sp. (WAM S34743). For labelling of structures see Fig. 3. Scale bar = 5 mm.
Figure 38 in Descriptions of New Species of the Diverse and Endemic Land Snail Amplirhagada Iredale, 1933 from Rainforest Patches across the Kimberley, Western Australia (Pulmonata: Camaenidae)
Figure 38. Genitalia of Amplirhagada bendraytoni n.sp. (WAM S34741). For labelling of structures see Fig. 3. Scale bar = 5 mm.
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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.