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1,445 results for “species richness.”

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Figure 3 in Species richness of urban and rural fish assemblages in the Grijalva Basin floodplain, southern Gulf of Mexico

Figure 3. – Fish distributed in the Villahermosa city and rural areas in the Grijalva floodplain. 1 – Anchoa mitchilli, 2 – Brevoortia gunteri, 3 – Hyphessobrycon compressus, 4 – Batrachoides goldmani, 5 – Dormitator maculatus, 6 – Eleotris amblyopsis, 7 – Gobiomorus dormitor, 8 – Oreochromis aureus, 9 – Rocio octofasciata, 10 – Thorichthys helleri, 11 – T. meeki, 12 – T. pasionis, 13 – Trichromis salvini, 14 – Atherinella alvarezi, 15 – Cynodonichthys tenuis, 16 – Belonesox belizanus, 17 – Carlhubbsia kidderi, 18 – Gambusia sexradiata, 19 – G. yucatana, 20 – Pseudoxiphophorus bimaculatus, 21 – Heterophallus echeagarayi, 22 – Phallichthys fairweatheri, 23 – Poecilia kykesis, 24 – P. mexicana. 25 – Xiphophorus maculatus, 26 – Achirus lineatus, and 27 – Microphis lineatus.

opencc-by-4.0Dec 2019View details →
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FIGURE 7 in Palaeoecology and sea level changes: Decline of mammal species richness during late Quaternary island formation in the Montebello Islands, north-western Australia

FIGURE 7. Spindle plot of the relative abundances of the species present in three or more spits in the Morgan's Cave deposit, plus all the species recorded in the Barrow Island owl pellet sample, showing the decrease in abundance of sand plain specialists such as Notomys alexis, and the increase in non-sand plain specialists such as Pseudomys nanus.

opencc-by-4.0Dec 2021View details →
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FIGURE 2. A in Palaeoecology and sea level changes: Decline of mammal species richness during late Quaternary island formation in the Montebello Islands, north-western Australia

FIGURE 2. A close-up map of Barrow and Montebello Islands, showing bathymetry of the area around the islands. The 10 m isohyet shows the outline of the "super-island", created when sea levels cut off the islands from the mainland and discussed below.

opencc-by-4.0Dec 2021View details →
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Fig. 1 in Evaluating the correlation between area, environmental heterogeneity, and species richness using terrestrial isopods (Oniscidea) from the Pontine Islands (West Mediterranean)

Fig. 1 Pontine archipelago. The geographic distance between Ventotene- Santo Stefano and the remaining islands is not in scale. 1, Scoglio Ravia; 2, Scoglio di Pilato; 3, Faraglioni della Madonna; 4, Scogli della Cantina; 5, Scoglio Cappello; 6, Faraglione di Mezzogiorno; 7, Le Galere

opencc-by-4.0Oct 2021View details →
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Supplementary material 1 from: Capinha C, Essl F, Seebens H, Pereira HM, Kühn I (2018) Models of alien species richness show moderate predictive accuracy and poor transferability. NeoBiota 38: 77-96. https://doi.org/10.3897/neobiota.38.23518

Table A1–A5 :

opencc-zeroJun 2018View details →
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FIGURE 6 in Deep-sea ascidians (Chordata, Tunicata) from the SW Atlantic: species richness with descriptions of two new species

FIGURE 6. Synoicum molle (Herdman, 1886): zooid.

opennotspecifiedNov 2018View details →
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FIGURE 9 in Deep-sea ascidians (Chordata, Tunicata) from the SW Atlantic: species richness with descriptions of two new species

FIGURE 9. Sycozoa umbellata (Michaelsen, 1898). A: colony; B: heads with zooids.

opennotspecifiedNov 2018View details →
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FIGURE 2 in Deep-sea ascidians (Chordata, Tunicata) from the SW Atlantic: species richness with descriptions of two new species

FIGURE 2. Aplidium meridianum (Sluiter, 1906). Colony.

opennotspecifiedNov 2018View details →
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FIGURE 1 in Deep-sea ascidians (Chordata, Tunicata) from the SW Atlantic: species richness with descriptions of two new species

FIGURE 1. Study area with details of the locations where samples were collected (stations 1–14).

opennotspecifiedNov 2018View details →
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FIGURE 13. Molgula pyriformis Herdman, 1881. A in Deep-sea ascidians (Chordata, Tunicata) from the SW Atlantic: species richness with descriptions of two new species

FIGURE 13. Molgula pyriformis Herdman, 1881. A: right gonad; B: left gonad.

opennotspecifiedNov 2018View details →
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FIGURE 5. Synoicum georgianum Sluiter, 1932 in Deep-sea ascidians (Chordata, Tunicata) from the SW Atlantic: species richness with descriptions of two new species

FIGURE 5. Synoicum georgianum Sluiter, 1932.

opennotspecifiedNov 2018View details →
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Supplementary material 1 from: Wölfling M, Uhl B, Fiedler K (2019) Multi-decadal surveys in a Mediterranean forest reserve – do succession and isolation drive moth species richness? Nature Conservation 35: 25-40. https://doi.org/10.3897/natureconservation.35.32934

: Data type: species data

opencc-zeroJun 2019View details →
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Figures 3-6 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938

Figures 3-6 Regression analysis across the entire gradient for average temperature with (3) estimated species richness, (4) Fisher's alpha, and regression analysis at the three highest elevations for average temperature with (5) estimated species richness, and (6) Fisher's alpha. (3) r2 = 0.5518, p = 0.150; (4) r2 = 0.7264, p = 0.067; (5) r2 = 0.9391, p = 0.159; (6) r2 = 0.7364, p = 0.343.

opencc-by-4.0Sep 2019View details →
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Figures 8-9 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938

Figures 8-9 Contribution of sphingid subfamilies to (8) species richness and (9) total abundance. Blue bars = Macroglossinae; orange bars = Sphinginae; grey bars = Smerinthinae. Contributions of each subfamily are similar among sites, and contributions of any particular subfamily to richness and abundance are similar within a site.

opencc-by-4.0Sep 2019View details →
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Figure 7 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938

Figure 7 Breakpoint regression analysis for (log)elevation with estimated species richness. Vitobamba (800 m), which was the break point, is included in both graphs. The characteristic mid-elevation unimodal richness pattern can be seen with the increase in species richness with elevation up to Vitobamba (r2 = 0.953, p = 0.139), and the decrease in species richness with elevation above Vitobamba (r2 = 0.999, p = 0.003).

opencc-by-4.0Sep 2019View details →
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Figure 2 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938

Figure 2 The relationship between elevation and species richness. There is a clear low-elevation skewed unimodal pattern, which peaks around 800 m.

opencc-by-4.0Sep 2019View details →
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Figures 9-16 from: Moreira GR.P, Pereira CM, Becker VO, Specht A, Gonçalves GL (2019) A new cecidogenous species of many-plumed moth (Alucitidae) associated with Cordiera A. Rich. ex DC. (Rubiaceae) in the Brazilian Cerrado. Zoologia 36: 1-15. https://doi.org/10.3897/zoologia.36.e34604

Figures 9-16 Male genitalia morphology of Prymnotomis cecidicola sp. nov. under light microscopy: (9, 11) general, lateral and ventral views, respectively (aedeagus omitted in Fig. 11); (10) valva, lateral (area marked with rectangle in Fig. 9); (12) aedeagus, lateral; (13) apex of uncus, ventral (indicated by asterisk in Fig. 11); (14) distal portion of gnathos (pointed by open arrow in Fig. 11); (15) arms of juxta, lateral (indicated by closed arrow in Fig. 11); (16) base of juxta (pointed by seta in Fig. 11). Scale bars; 200, 100, 200, 200, 100, 100, 70, 100 µm, respectively.

opencc-by-4.0Nov 2019View details →
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Figure 24-34 from: Moreira GR.P, Pereira CM, Becker VO, Specht A, Gonçalves GL (2019) A new cecidogenous species of many-plumed moth (Alucitidae) associated with Cordiera A. Rich. ex DC. (Rubiaceae) in the Brazilian Cerrado. Zoologia 36: 1-15. https://doi.org/10.3897/zoologia.36.e34604

Figure 24-34 Morphology of Prymnotomis cecidicola sp. nov. last larval instar under scanning electron microscopy: (24) head, lateral view; (25) labrum, dorsal; (26) antenna, lateral; (27) latero-dorsal area of head in detail; (28) maxillae and labium, antero-ventral; (29) labium in detail (area marked by rectangle in Fig. 28; asterisk indicates associated flap-like protrusions of stipes); (30) mesothoracic leg, postero-lateral; (31) tarsal claw in detail, posterior (open arrow indicates basal spine); (32) prothoracic spiracle, lateral; (33) proleg of fifth abdominal segment, lateral; (34) last two abdominal segments, lateral. Scale bars: 200, 50, 50, 50, 100, 25, 100, 25, 50, 50, 200 µm; 0.5, 0.5, 0.5 mm, respectively.

opencc-by-4.0Nov 2019View details →
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Figures 17-19 from: Moreira GR.P, Pereira CM, Becker VO, Specht A, Gonçalves GL (2019) A new cecidogenous species of many-plumed moth (Alucitidae) associated with Cordiera A. Rich. ex DC. (Rubiaceae) in the Brazilian Cerrado. Zoologia 36: 1-15. https://doi.org/10.3897/zoologia.36.e34604

Figures 17-19 Female genitalia morphology of Prymnotomis cecidicola sp. nov. under light microscopy: (17) general view, ventral; (18, 19) detail of corpus bursae and papillae anales, respectively (areas marked with rectangles in Fig. 17). Scale bars: 200, 30, 50 µm, respectively.

opencc-by-4.0Nov 2019View details →
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Figure 1 from: Moreira GR.P, Pereira CM, Becker VO, Specht A, Gonçalves GL (2019) A new cecidogenous species of many-plumed moth (Alucitidae) associated with Cordiera A. Rich. ex DC. (Rubiaceae) in the Brazilian Cerrado. Zoologia 36: 1-15. https://doi.org/10.3897/zoologia.36.e34604

Figure 1 Maximum likelihood tree based on COI sequences for 41 Alucitidae species and lineages – ln likelihood = 5937. The phylogenetic position of Prymnotomis cecidicola sp. nov. (CMP 008) is indicated in orange. Bootstrap values are indicated for nodes with more than 50% support (1000 replications).

opencc-by-4.0Nov 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