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Plate 3. Figures 21-28. Chimarra spp. Male genitalia. 21-25. Chimarra biungulata. 21. Lateral view, 22 in Genus Chimarra Stephens, 1829 (Insecta: Trichoptera: Philopotamidae) from Suntalekhola Biodiversity Camp, Neora Valley, National Park, West Bengal
Plate 3. Figures 21-28. Chimarra spp. Male genitalia. 21-25. Chimarra biungulata. 21. Lateral view, 22. Dorsal view,
FIGURE 7 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids
FIGURE 7 | Type-locality of Moenkhausia cambacica, tributary of igarapé Ávila, upper rio Machado, rio Madeira basin, Vilhena, Rondônia, Brazil.
FIGURE 6 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids
FIGURE 6 | Distribution of Moenkhausia cambacica in the upper rio Machado, rio Madeira basin, Brazil. Black star (type-locality), blue star (other localities).
FIGURE 5 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids
FIGURE 5 | Paratypes of Moenkhausia cambacica, MZUSP 125793, freshly collected, showing other aspects of its live coloration, Brazil, Rondônia State, Municipality of Vilhena, rio Madeira basin, upper rio Machado drainage.
FIGURE 3 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids
FIGURE 3 | Schematic drawing of Moenkhausia cambacica showing A. lateral-line perforation pattern observed in most specimens. B. Morphology of the lateral-line scales above anal fin: I – scale lacking tube and pore; II – scale with poorly developed tube, with small tube walls; III – scale with poorly developed tube, walls larger but not enclosed; IV– scale with fully developed bony tube, tube walls enclosed, with a posterior pore.
FIGURE 4 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids
FIGURE 4 | Live coloration of Moenkhausia cambacica, paratype, MZUSP 125793, Brazil, Rondônia State, Municipality of Vilhena, rio Madeira basin, upper rio Machado drainage.
FIGURE 1 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids
FIGURE 1 | Holotype of Moenkhausia cambacica, MZUSP 125792, 34.8 mm SL, Brazil, Rondônia State, Municipality of Vilhena, rio Madeira basin, upper rio Machado drainage.
FIGURE 2 in A new species of Moenkhausia (Characiformes: Characidae) from the rio Madeira basin, Brazil, with comments on the evolution and development of the trunk lateral line system in characids
FIGURE 2 | Medial view of left side, premaxillary, maxillary, and dentary of Moenkhausia cambacica, MZUSP 125793, 27.1 mm SL, paratype. Scale bar: 1 mm.
Figures 113–118 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 113–118: SEM images of the marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (113, 114) Cocconeis orbicularis, external and internal faces of sternum valve. (115, 116) Fragilariopsis cylindrus, internal valve sides. (117) Entomoneis paludosa. (118) Nitzschia australis.
Figures 60–78 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 60–78: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (60, 61) Cocconeis antigua. (62) Diploneis smithii. (63) Diploneis weissflogii. (64) Diploneis sp. (65) Caloneis sp. (66, 67) Navicula cancellate. (68) Navicula directa. (69, 70) Navicula perminuta. (71) Navicula sp. (72, 73) Pseudogomphonema kamtchaticum. (74) Trachyneis aspera. (75, 76) Biremis ambigua. (77) Parlibellus crucicula. (78) Pinnularia quadratarea.
Figures 12–19 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 12–19: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (12) Coscinodiscus radiatus. (13–16) Stellarima microtrias, figures showing variable number of central rimoportulae. (17) Asteromphalus parvulus. (18) Paralia sulcata. (19) Podosira stelliger.
Figures 93–106 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 93–106: Marine benthic diatoms in Potter Cove, King George Island, Antarctica in summer 2015. (93) Nitzschia angularis. (94, 95) Nitzschia australis. (96) Nitzschia mitchelliana. (97) Nitzschia cf. gelida. (98) Nitzschia hybrida. (99) Nitzschia cf. obtusa. (100) Nitzschia sigma. (101) Nitzschia sp. (102) Entomoneis gigantea. (103) Entomoneis kjellmanii. (104) Entomoneis paludosa. (105) Surirella fastuosa. (106) Surirella sp.
Figures 39–59 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 39–59: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (39) Lyrella hennedyi. (40) Petroneis sp. (41) Petroneis plagiostoma. (42) Staurophora sp. (43–46) Achnanthes cf. groenlandica, (43, 44) raphe valve, (45) sternum valve, (46) two cells in girdle view. (47) Cocconeis californica. (48) Cocconeis californica var. kerguelensis. (49) Cocconeis costata var. hexagona. (50) Cocconeis dallmannii. (51) Cocconeis fasciolata. (52) Cocconeis imperatrix. (53) Cocconeis matsii. (54, 55) Cocconeis melchioroides. (56–59) Cocconeis orbicularis, (56, 59) sternum valve, (57, 58) raphe valve.
Figures 20–26 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 20–26: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (20, 21) Actinocyclus actinochilus. (22) Trigonium arcticum. (23) Triceratium favus. (24–26) Odontella litigiosa.
Figures 2–11 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 2–11: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (2–4) Porosira glacialis. (5) Thalassiosira eccentrica. (6) Thalassiosira gracilis. (7) Thalassiosira oliveriana. (8) Thalassiosira sp. (9, 10) Melosira sol, (10) showing chain of cells in girdle view. (11) Melosira cf. adeliae.
Figures 107–112 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 107–112: SEM images of the marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (107, 108) Porosira glacialis, internal valve view showing the single marginal labiate process. (109–111) Entopyla ocellata, (109, 110) external valve view showing the wide and superficial apical porefield which occupies large area of valve face, (111) internal valve structure showing the narrow and crescent-like rimoportula openings (white arrows). (112) Navicula sp. 2.
Figures 27–38 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 27–38: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (27) Corethron pennatum. (28) Fragilaria striatula. (29) Synedropsis sp. (30) Licmophora antarctica. (31–32) Licmophora belgicae. (33) Licmophora gracilis. (34) Licmophora luxuriosa. (35) Thalassionema nitzschioides. (36) Rhabdonema arcuatum. (37, 38) Entopyla ocellata.
Figures 79–92 in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
Figures 79–92: Marine benthic diatoms in Potter Cove, King George Island, Antarctica, summer 2015. (79) Gyrosigma arcuatum. (80) Gyrosigma fasciola. (81) Gyrosigma cf. obscurum. (82) Pleurosigma eudon var. kerguelensis. (83) Pleurosigm diversestriatum. (84) Pleurosigma strigosum. (85) Amphora gourdonii. (86) Amphora marina. (87, 88) Amphora sp. 1. (89) Amphora sp. 2. (90) Cylindrotheca closterium. (91, 92) Fragilariopsis cylindrus.
Lobelia appendiculata var. gattingeri (Campanulaceae) - inflorescence - lateral view of flower
Image of Lobelia appendiculata var. gattingeri (Campanulaceae) - inflorescence - lateral view of flower
Delphinium carolinianum ssp. calciphilum (Ranunculaceae) - inflorescence - lateral view of flower
Image of Delphinium carolinianum ssp. calciphilum (Ranunculaceae) - inflorescence - lateral view of flower
ScienceDex guides
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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.