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3,507 results for “Species identification”

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zenodo28/100

Figure 2 from: Dorado-Roncancio J, Gaviria S, Bernal-De La Torre L, Ahrens MJ (2019) A new species of Bestiolina (Crustacea, Copepoda, Calanoida, Paracalanidae) from coastal waters of the Colombian Pacific, including a worldwide key for the identification of the species. ZooKeys 846: 1-18. https://doi.org/10.3897/zookeys.846.31497

Figure 2 Female Holotype of Bestiolinasarae sp. n. A habitus, dorsal view and digital photograph B rostrum C posterolateral margins of fifth pedigerous somite, lateral view D second and third urosomites and anal somite with caudal rami E caudal rami and setae. Scales bar: 0.1 mm (A, D); 0.01 mm (B, E); 0.05 mm (C).

opencc-by-4.0May 2019View details →
zenodo28/100

Figure 4 from: Dorado-Roncancio J, Gaviria S, Bernal-De La Torre L, Ahrens MJ (2019) A new species of Bestiolina (Crustacea, Copepoda, Calanoida, Paracalanidae) from coastal waters of the Colombian Pacific, including a worldwide key for the identification of the species. ZooKeys 846: 1-18. https://doi.org/10.3897/zookeys.846.31497

Figure 4 Female of Bestiolinasarae sp. n. A Leg 1, anterior view, Leg 1 and digital photograph B leg 2, posterior view and digital photograph C leg 3, anterior view (spinules on posterior surface not indicated in contrast with leg 2) and digital photograph D leg 4, anterior view and digital photograph E leg 5 and digital photograph. Scales bars: 0.05 mm (A–D); 0.01 mm (E).

opencc-by-4.0May 2019View details →
zenodo28/100

Figure 3 from: Dorado-Roncancio J, Gaviria S, Bernal-De La Torre L, Ahrens MJ (2019) A new species of Bestiolina (Crustacea, Copepoda, Calanoida, Paracalanidae) from coastal waters of the Colombian Pacific, including a worldwide key for the identification of the species. ZooKeys 846: 1-18. https://doi.org/10.3897/zookeys.846.31497

Figure 3 Female Holotype of Bestiolinasarae sp. n. A antennule B antenna C mandible D maxillule E maxilla F maxilliped. Scales bars: 0.1 mm (A); 0.05 mm (B–F).

opencc-by-4.0May 2019View details →
zenodo28/100

FIGURES 12–13 in A new species of Nothobrya Arlé, 1961 (Collembola: Entomobryidae) from Brazil and notes on key characters for Nothobryinae taxonomy, with an identification key to the species of the subfamily

FIGURES 12–13. Nothobrya sertaneja sp. nov., body dorsal chaetotaxy: 12, Th. II; 13, Th. III.

opennotspecifiedJun 2019View details →
zenodo28/100

FIGURE 1 in A new species of Nothobrya Arlé, 1961 (Collembola: Entomobryidae) from Brazil and notes on key characters for Nothobryinae taxonomy, with an identification key to the species of the subfamily

FIGURE 1. Symbols used in dorsal chaetotaxy description of Nothobrya sertaneja sp. nov.

opennotspecifiedJun 2019View details →
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FIGURE 2 in A new species of Nothobrya Arlé, 1961 (Collembola: Entomobryidae) from Brazil and notes on key characters for Nothobryinae taxonomy, with an identification key to the species of the subfamily

FIGURE 2. Nothobrya sertaneja sp. nov.: habitus in 70% ethanol, lateral view.

opennotspecifiedJun 2019View details →
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F I G U R E 2 in Machine learning for image based species identification

F I G U R E 2 Comparison between biological and artificial neuron and networks

opennotspecifiedDec 2018View details →
zenodo28/100

FIGURE 1 in Marine mites (Acari: Hydrachnidia) of the Mediterranean Sea: Descriptions of two new species, key for identification and future prospects

FIGURE 1. Map of the study area (Antalya, Turkey).

opennotspecifiedApr 2019View details →
zenodo28/100

Supplementary material 1 from: Li Y, Li H, Motokawa M, Wu Y, Harada M, Sun H, Mo X, Wang J, Li Y (2019) A revision of the geographical distributions of the shrews Crocidura tanakae and C. attenuata based on genetic species identification in the mainland of China. ZooKeys 869: 147-160. https://doi.org/10.3897/zookeys.869.33858

: Data type: species data

opencc-zeroAug 2019View details →
zenodo28/100

FIGURE 11 in A new species of Nothobrya Arlé, 1961 (Collembola: Entomobryidae) from Brazil and notes on key characters for Nothobryinae taxonomy, with an identification key to the species of the subfamily

FIGURE 11. Nothobrya sertaneja sp. nov., dorsal head chaetotaxy.

opennotspecifiedJun 2019View details →
zenodo28/100

FIGURES 17–18 in A new species of Nothobrya Arlé, 1961 (Collembola: Entomobryidae) from Brazil and notes on key characters for Nothobryinae taxonomy, with an identification key to the species of the subfamily

FIGURES 17–18. Nothobrya sertaneja sp. nov., body dorsal chaetotaxy: 17, Abd. IV; 18, Abd. V.

opennotspecifiedJun 2019View details →
zenodo28/100

Figures 3-4 from: Balkenohl M (2017) Trilophidius gemmatus sp. n., a new species from Bhutan, with an updated identification key to the Asian species (Coleoptera, Carabidae, Scaritinae). Alpine Entomology 1: 51-56. https://doi.org/10.3897/alpento.1.17351

Figures 3-4 - Trilophidius gemmatus sp. n., holotype, male genitalia. 3 Overview of the aedeagus with median lobe and parameres, dorsolateral view. 4 Median lobe showing the internal structures of the aedeagus, ventral view.

opencc-by-4.0Nov 2017View details →
zenodo28/100

Figure 1 from: Schneider SA, Fizdale MA, Normark BB (2019) An online interactive identification key to common pest species of Aspidiotini (Hemiptera, Coccomorpha, Diaspididae), version 1.0. ZooKeys 867: 87-96. https://doi.org/10.3897/zookeys.867.34937

Figure 1 Aspidiotine general morphology. This diagram exemplifies a composite aspidiotine species, illustrating major anatomical features, body segmentation, and traits that a user would encounter in the key. The illustration orients users to the appearance of slide-mounted specimens and terminology used to describe their features. The illustration is based on a similar image presented by Miller and Davidson (2005), their Figure 3. Illustration by Taina Litwak.

opencc-by-4.0Oct 2019View details →
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Figure 3 from: Schneider SA, Fizdale MA, Normark BB (2019) An online interactive identification key to common pest species of Aspidiotini (Hemiptera, Coccomorpha, Diaspididae), version 1.0. ZooKeys 867: 87-96. https://doi.org/10.3897/zookeys.867.34937

Figure 3 Abdominal segmentation. This diagram shows pygidial segmentation as it is defined for the purposes of this key. The panels highlight (A) the pygidium (B) abdominal segment 8 (C) abdominal segment 7 (D) abdominal segment 6 and (E) abdominal segment 5. Illustrations by Taina Litwak.

opencc-by-4.0Oct 2019View details →
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Figure 2 from: Schneider SA, Fizdale MA, Normark BB (2019) An online interactive identification key to common pest species of Aspidiotini (Hemiptera, Coccomorpha, Diaspididae), version 1.0. ZooKeys 867: 87-96. https://doi.org/10.3897/zookeys.867.34937

Figure 2 Aspidiotine pygidial morphology. This diagram provides an enlarged view of the general pygidial morphology of aspidiotines. This serves as another guide to the appearance of anatomical features and their terminology. Illustration by Taina Litwak.

opencc-by-4.0Oct 2019View details →
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Figure 5 from: Li Y, Li H, Motokawa M, Wu Y, Harada M, Sun H, Mo X, Wang J, Li Y (2019) A revision of the geographical distributions of the shrews Crocidura tanakae and C. attenuata based on genetic species identification in the mainland of China. ZooKeys 869: 147-160. https://doi.org/10.3897/zookeys.869.33858

Figure 5 Comparison of teeth of Crocidura attenuata (left: S2576) and Crocidura tanakae (right: S2566) from Baoxing, Sichuan.

opencc-by-4.0Oct 2019View details →
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Figure 2 from: Li Y, Li H, Motokawa M, Wu Y, Harada M, Sun H, Mo X, Wang J, Li Y (2019) A revision of the geographical distributions of the shrews Crocidura tanakae and C. attenuata based on genetic species identification in the mainland of China. ZooKeys 869: 147-160. https://doi.org/10.3897/zookeys.869.33858

Figure 2 ML tree based on Cytb of Crocidura genus. Numbers above the branches represent bootstrap support (BS). The blue clade represents C. tanakae and orange clade represents C. attenuata.

opencc-by-4.0Oct 2019View details →
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Figure 4 from: Li Y, Li H, Motokawa M, Wu Y, Harada M, Sun H, Mo X, Wang J, Li Y (2019) A revision of the geographical distributions of the shrews Crocidura tanakae and C. attenuata based on genetic species identification in the mainland of China. ZooKeys 869: 147-160. https://doi.org/10.3897/zookeys.869.33858

Figure 4 Comparison of crania of Crocidura attenuata (S2576) and Crocidura tanakae (S2566) from Baoxing, Sichuan. Top row from left to right: dorsal views of the skulls of C. attenuata and C. tanakae (S2576 andS2566), ventral views of the skulls in the same order. Lower row: lateral view of skulls and mandibles from top to bottom of C. attenuata and C. tanakae (S2576 and S2566).

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 6 from: Li Y, Li H, Motokawa M, Wu Y, Harada M, Sun H, Mo X, Wang J, Li Y (2019) A revision of the geographical distributions of the shrews Crocidura tanakae and C. attenuata based on genetic species identification in the mainland of China. ZooKeys 869: 147-160. https://doi.org/10.3897/zookeys.869.33858

Figure 6 Scatter plot of C. attenuata (red) and C. tanakae (blue) sample distribution over PC1 and PC2 axes constructed based on external and skull morphological variables. Different symbols represent different populations. GD: Guangdong, FJ: Fujian, ZJ: Zhejiang, SCBX: Baoxing, Sichuan, HB: Hubei, SC: Sichuan, GX: Guangxi, AH: Anhui, HuN: Hunan, HN: Hainan, CQ: Chongqing, YN: Yunnan, JX: Jiangxi

opencc-by-4.0Oct 2019View details →
zenodo28/100

Figure 3 from: Li Y, Li H, Motokawa M, Wu Y, Harada M, Sun H, Mo X, Wang J, Li Y (2019) A revision of the geographical distributions of the shrews Crocidura tanakae and C. attenuata based on genetic species identification in the mainland of China. ZooKeys 869: 147-160. https://doi.org/10.3897/zookeys.869.33858

Figure 3 Distributions of Crocidura attenuata and C. tanakae in the mainland of China,Laos and Vietnam. Black and white triangles represent the sampled sites of C. tanakae first presented in this study and in previous studies, respectively. White circles and squares represent the sampled sites of C. attenuata first presented in this study and in previous studies. Black triangles and white circles overlapped indicate sympatry sites.

opencc-by-4.0Oct 2019View 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