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zenodo28/100

Figures 5-8 from: Sharaf MR, Collingwood CA, Al Dhafer HM, Al mutairi MS, Aldawood AS (2015) New synonyms of two Arabian ants of the genus Monomorium Mayr, 1855 (Hymenoptera, Formicidae). ZooKeys 505: 51-58. https://doi.org/10.3897/zookeys.505.9441

Figures 5-8 - Monomorium subopacum (paralectotype worker), CASENT0010949. 5 Body in profile 6 Body in dorsal view 7 Head in full-face view 8 specimen label Photo April Nobile, http://antweb.org/

opencc-by-4.0May 2015View details →
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Figures 1-4 from: Sharaf MR, Collingwood CA, Al Dhafer HM, Al mutairi MS, Aldawood AS (2015) New synonyms of two Arabian ants of the genus Monomorium Mayr, 1855 (Hymenoptera, Formicidae). ZooKeys 505: 51-58. https://doi.org/10.3897/zookeys.505.9441

Figures 1-4 - Monomorium exiguum (worker), CASENT0101870. 1 Body in profile 2 Body in dorsal view 3 Head in full-face view 4 specimen label. Photo Zach Lieberman, http://antweb.org/

opencc-by-4.0May 2015View details →
zenodo28/100

Figure 4 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137

Figure 4 - Spatial distribution maps of Hypena sp. demonstrating different densities between seasons. In the dry seasons (17/07/1999 and 10/07/2000) individuals are located in the deepest region of the cave, an opposite pattern during rainy seasons (16/01/2000 and 19/01/2001) when the population of individuals becomes denser in the region near the cave entrance. Blue colors indicate low densities while light yellow colors indicate high densities.

opencc-by-4.0Jul 2015View details →
zenodo28/100

Figure 1 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137

Figure 1 - A Photograph indicating the cave entrance and the surrounding region, whose native forest was turned into pasture B Conduit located in the area near the entrance C Individuals of Hypena sp. resting on the cave wall.

opencc-by-4.0Jul 2015View details →
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Figure 3 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137

Figure 3 - Spatial Point Pattern Analysis of the second monitoring (January 2000). A Dot map and (B), shows the estimations of the function K (r is the distance argument, Dashed line corresponds to the theoretical value of this function is Complete Spatial Randomness and solid lineis the Observed value of the K function for the date pattern) C Map Kernel Estimates of intensity.

opencc-by-4.0Jul 2015View details →
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Figure 2 from: Ferreira RL, Martins VM, Paixão ER, Silva MS (2015) Spatial and temporal fluctuations of the abundance of Neotropical cave-dwelling moth Hypena sp. (Noctuidae, Lepidoptera) influenced by temperature and humidity. Subterranean Biology 16: 47-60. https://doi.org/10.3897/subtbiol.16.5137

Figure 2 - A Variation in temperature and humidity along the Taboa cave, showing a tendency to stabilize in the deeper parts of the cave. The table shows the section in which the Hypena sp specimens were collected (B) Change in abundance over the transects, the arrow indicates the spatial extent where the effects of the surface seasonality promote decrease and expansion in the population distribution.

opencc-by-4.0Jul 2015View details →
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Figure 4 from: Caterino MS, Tishechkin AK (2016) Spatial and environmental correlates of species richness and turnover patterns in European cryptocephaline and chrysomeline beetles. ZooKeys 557: 59-77. https://doi.org/10.3897/zookeys.557.7087

Figure 4 - Female genitalia, Megalocraerus rubricatus. A 8th tergite, dorsal view B 8th sternite, ventral view C Bursa copulatrix (bc), common oviduct (co), spermatheca (st) and attached spermathecal gland (stg) D Ovipositor.

opencc-by-4.0Jan 2016View details →
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Figure 3 from: Caterino MS, Tishechkin AK (2016) Spatial and environmental correlates of species richness and turnover patterns in European cryptocephaline and chrysomeline beetles. ZooKeys 557: 59-77. https://doi.org/10.3897/zookeys.557.7087

Figure 3 - Male genitalia, Megalocraerus rubricatus. A 8th tergite, dorsal view B 8th sternite, dorsal view C 8th tergite and sternite, lateral view, in situ D 9th and 10th tergites, dorsal view E 9th sternite, dorsal view F Aedeagus, dorsal view G Tegmen, lateral view.

opencc-by-4.0Jan 2016View details →
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Figure 6 from: Caterino MS, Tishechkin AK (2016) Spatial and environmental correlates of species richness and turnover patterns in European cryptocephaline and chrysomeline beetles. ZooKeys 557: 59-77. https://doi.org/10.3897/zookeys.557.7087

Figure 6 - Aedeagi of Megalocraerus spp. A Megalocraerus mandibularis, dorsal view B Megalocraerus mandibularis, lateral view C Megalocraerus chico, dorsal view D Megalocraerus chico, lateral view E Megalocraerus madrededios, dorsal view F Megalocraerus madrededios, lateral view G unnamed Megalocraerus sp. from Rio de Janeiro, dorsal view H unnamed Megalocraerus sp. from Rio de Janeiro, lateral view.

opencc-by-4.0Jan 2016View details →
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Figure 1 from: Caterino MS, Tishechkin AK (2016) Spatial and environmental correlates of species richness and turnover patterns in European cryptocephaline and chrysomeline beetles. ZooKeys 557: 59-77. https://doi.org/10.3897/zookeys.557.7087

Figure 1 - Generic characters of Megalocraerus. A Frons B Antenna C Mouthparts, ventral view (one maxilla and labial palpus omitted for clarity).

opencc-by-4.0Jan 2016View details →
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Figure 5 from: Caterino MS, Tishechkin AK (2016) Spatial and environmental correlates of species richness and turnover patterns in European cryptocephaline and chrysomeline beetles. ZooKeys 557: 59-77. https://doi.org/10.3897/zookeys.557.7087

Figure 5 - A Dorsal habitus Megalocraerus mandibularis B Mandibles male Megalocraerus mandibularis C Dorsal habitus Megalocraerus chico.

opencc-by-4.0Jan 2016View details →
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Figures 3-6 from: Breitkreuz LCV, Winterton SL, Engel MS (2015) Revision of the green lacewing subgenus Ankylopteryx (Sencera) (Neuroptera, Chrysopidae). ZooKeys 543: 111-127. https://doi.org/10.3897/zookeys.543.6476

Figures 3-6 - Photographs of forewings of Ankylopteryx (Sencera) anomala (Brauer) 3 Lectotype male from Pulo Milu, Nicobar Islands, India (NHMW) (photograph by Harald Bruckner) 4 Holotype male (mirrored) of 'Sencera exquisita Nakahara' from Taiwan, China (NMNS) (photograph by Utsugi Jinbo) 5 Holotype male (mirrored) of 'Sencera feae Navás' from Bhamò, Myanmar (MCSN) (photograph by Maria Tavano) 6 Holotype male (mirrored) of 'Sencera scioneura Navás' from New Britain, Papua New Guinea (ZMB) (photograph by Lukas Kirschey). All photographs used with permission.

opencc-by-4.0Dec 2015View details →
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Figures 7-10 from: Breitkreuz LCV, Winterton SL, Engel MS (2015) Revision of the green lacewing subgenus Ankylopteryx (Sencera) (Neuroptera, Chrysopidae). ZooKeys 543: 111-127. https://doi.org/10.3897/zookeys.543.6476

Figures 7-10 - Photographs of forewings of Ankylopteryx (Sencera) anomala (Brauer) showing gradations in wing colouration, from almost unmarked (7), to slightly marked (8), to more strongly marked (9), and ultimately to very strongly marked (10). Specimens from Vanuatu (7), Brunei (8), Myanmar (9), and Hainan, China (10). All photographs by L.C.V.B.

opencc-by-4.0Dec 2015View details →
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Figure 1 from: Breitkreuz LCV, Winterton SL, Engel MS (2015) Revision of the green lacewing subgenus Ankylopteryx (Sencera) (Neuroptera, Chrysopidae). ZooKeys 543: 111-127. https://doi.org/10.3897/zookeys.543.6476

Figure 1 - Photograph of live male of Ankylopteryx (Sencera) anomala (Brauer) from Chiang Mai, Thailand (photograph by S.L. Winterton).

opencc-by-4.0Dec 2015View details →
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Figures 14 from: Breitkreuz LCV, Winterton SL, Engel MS (2015) Revision of the green lacewing subgenus Ankylopteryx (Sencera) (Neuroptera, Chrysopidae). ZooKeys 543: 111-127. https://doi.org/10.3897/zookeys.543.6476

Figures 14 - Photograph of a live male of Ankylopteryx (Sencera) anomala (Brauer) from Kuala Lumpur, Malaysia at a flower of an unidentified orchid species of the genus Bulbophyllum Thouars (Orchidaceae: Epidendroideae) (photograph by P.T. Ong, used with permission).

opencc-by-4.0Dec 2015View details →
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Figures 11-13 from: Breitkreuz LCV, Winterton SL, Engel MS (2015) Revision of the green lacewing subgenus Ankylopteryx (Sencera) (Neuroptera, Chrysopidae). ZooKeys 543: 111-127. https://doi.org/10.3897/zookeys.543.6476

Figures 11-13 - Male and female terminalia of Ankylopteryx (Sencera) anomala (Brauer). 11 Line drawing of male genitalic sclerites 12 Lateral view of male abdominal apex with genitalia 13 Lateral view of female abdominal apex with genitalia.

opencc-by-4.0Dec 2015View details →
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Figure 7 from: Marques R, Mebert K, Fonseca É, Rödder D, Solé M, Tinôco MS (2016) Composition and natural history notes of the coastal snake assemblage from Northern Bahia, Brazil. ZooKeys 611: 93-142. https://doi.org/10.3897/zookeys.611.9529

Figure 7 - Strongly marked polymorphism of Bothrops lutzi from São Desidério, Bahia (A) and Grande Sertão Veredas National Park, Minas Gerais (B) (Photos A by R. Gaiga; B by M. Sacramento).

opencc-by-4.0Aug 2016View details →
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Figure 6 from: Marques R, Mebert K, Fonseca É, Rödder D, Solé M, Tinôco MS (2016) Composition and natural history notes of the coastal snake assemblage from Northern Bahia, Brazil. ZooKeys 611: 93-142. https://doi.org/10.3897/zookeys.611.9529

Figure 6 - Dipsadids, elapids and viperids from north coast of Bahia: A Erythrolamprus miliaris merremi B Erythrolamprus poeilogyrus schotti (juvenile with a Erythrolamprus poeilogyrus poecilogyrus-like pattern) C Erythrolamprus poecilogyrus schotti (adult) D Erythrolamprus reginae semilineatus, E Erythrolamprus taeniogaster F Erythrolamprus viridis viridis G Xenodon merremii H Xenodon rhabdocephalus rhabdocephalus I Micrurus corallinus J Micrurus ibiboboca K Bothrops erythromelas L Bothrops leucurus M Bothrops lutzi N Crotalus durissus cascavella O Lachesis muta rhombeata (Photos F, G, K by M.L.O. Travassos; O by W. Pessoa).

opencc-by-4.0Aug 2016View details →
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Figure 5 from: Marques R, Mebert K, Fonseca É, Rödder D, Solé M, Tinôco MS (2016) Composition and natural history notes of the coastal snake assemblage from Northern Bahia, Brazil. ZooKeys 611: 93-142. https://doi.org/10.3897/zookeys.611.9529

Figure 5 - Dipsadids from the northern coast of Bahia: A Sibynomorphus neuwiedi B Imantodes cenchoa cenchoa C Leptodeira annulata annulata D Taeniophallus occipitalis E Helicops angulatus F Helicops leopardinus G Philodryas nattereri H Philodryas olfersii herbeus I Philodryas patagoniensis J Clelia plumbea K Oxyrhopus petolarius digitalis L Oxyrhopus trigeminus M Phimophis guerini N Pseudoboa nigra O Siphlophis compressus P Thamnodynastes pallidus Q Erythrolamprus aesculapii venustissimus R Erythrolamprus almadensis.

opencc-by-4.0Aug 2016View details →
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Figure 4 from: Marques R, Mebert K, Fonseca É, Rödder D, Solé M, Tinôco MS (2016) Composition and natural history notes of the coastal snake assemblage from Northern Bahia, Brazil. ZooKeys 611: 93-142. https://doi.org/10.3897/zookeys.611.9529

Figure 4 - Typhlopid, boids and colubrids from the northern coast of Bahia: A Amerotyphlops brongersmianus B Boa constrictor constrictor C Corallus hortulanus D Epicrates assisi E Eunectes murinus F Chironius bicarinatus G Chironius carinatus H Chironius exoletus I Chironius flavolineatus J Drymarchon corais K Drymoluber dichrous (juvenile) L Leptophis ahaetulla liocercus M Mastigodryas bifossatus N Oxybelis aeneus O Pantherophis guttatus P Pseustes sulphureus sulphureus Q Spilotes pullatus pullatus R Tantilla melanocephala. (Photo F by M. A. Passos; D by W. Pessoa; J, K by M. L. O. Travassos).

opencc-by-4.0Aug 2016View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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