Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
836
datasets available to search
ShareScore release 0.9.0
Dataset results
836 results for “species limits”
Fig 5 in Morphological and ecological convergence at the lower size limit for vertebrates highlighted by five new miniaturised microhylid frog species from three different Madagascan genera
Fig 5. One-second spectrograms and oscillograms of the calls of the new species described here. Insets represent the respective species but not the calling specimens. (a) Mini mum gen. et sp. nov., paratype ZMB 81993 from Manombo, (b) Mini scule gen. et sp. nov., ZSM 265/2018 from Sainte Luce, (c) Rhombophryne proportionalis sp. nov., part of a call (note series) of a specimen from Bepia campsite, Tsaratanana (not collected), (d) Anodonthyla eximia sp. nov., specimen not collected, from Maharira (Ranomafana). https://doi.org/10.1371/journal.pone.0213314.g005
Fig 3 in Morphological and ecological convergence at the lower size limit for vertebrates highlighted by five new miniaturised microhylid frog species from three different Madagascan genera
Fig 3. Currently known localities of the new taxa described in this paper. The base map is USGS SRTM 1-Arc second digital elevation model. https://doi.org/10.1371/journal.pone.0213314.g003
FIGURE 11. Badis rhabdotus. A in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 11. Badis rhabdotus. A, holotype, DU 9035, adult male, 46.9 mm SL; B paratype, NRM 68599, adult female, 37.2 mm SL; C, paratype, NRM 69034, adult female, 39.7 mm SL, preserved in 95% ethanol. All from Bangladesh, Pyain River at Jaflong.
FIGURE 10 in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 10. Shailopropat Falls in the dry season, looking down from above the middle of the falls. Badis pallidus was collected from the small stream at the bottom of the ravine.
FIGURE 7. Badis chittagongis. A in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 7. Badis chittagongis. A, adult male, NRM 68074, 40.8 mm SL; B, adult female, 35.0 mm SL; Both from Bangladesh: Barachora stream, 4 km south of Cox′s Bazar; C adult male, NRM 68040, 37.8 mm SL, from Bangladesh: Maheshkhali Island, Khaler Uttarkul.
FIGURE 5. Badis badis. NRM 68307. A in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 5. Badis badis. NRM 68307. A, male, 34.1 mm SL; B, female, 28.5 mm SL. Both from Bangladesh, Fenchuganj, roadside ditch 4 km south of Sylhet.
FIGURE 6 in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 6. Comparison of relative size trajectories of interorbital width against standard length in species of Badis reported from Bangladesh.
FIGURE 4 in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 4. Collecting site of Badis badis and Dario kajal, a roadside ditch close to Sylhet. To the right a large rice paddy. Specimens were collected from dense vegetation dominated by water hyacinths. Photo taken after fishing activities leaving an open area in the otherwise covering vegetation.
FIGURE 1f in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 1f. clustering of sequences representing the genus Dario. Excerpt from mPTP delimitation tree of species of the Badidae, based on coi sequences (Fig. S3). New sequences are labeled with tissue collection identifiers in NRM. Sequences from GenBank are labeled with Accession number and original determination
FIGURE 1e in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 1e. clustering of sequences representing Badis from the Brahmaputra River: Badis laspiophilus, B. singenensis, B. "Sonitpur", and an unidentified species from the Ranganadi River. Excerpt from mPTP delimitation tree of species of the Badidae, based on coi sequences (Fig. S3). New sequences are labeled with tissue collection identifiers in NRM and DU. Sequences from GenBank are labeled with Accession number and original determination.
FIGURE 1d in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 1d. clustering of sequences representing Badis rhabdotus and Badis sp "Kolodyne". Badis sp. Excerpt from bPTP delimitation tree of species of the Badidae, based on coi sequences (Fig. S3). New sequences are labeled with tissue collection identifiers in NRM. Sequences from GenBank are labeled with Accession number and original determination.
FIGURE 1c in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 1c. clustering of sequences representing Badis pallidus, B. chittagongis, and an unidentified OTU from the Yamuna River. Excerpt from bPTP delimitation tree of species of the Badidae, based on coi sequences (Fig S3). New sequences are labeled with tissue collection identifiers in NRM and DU. Sequences from GenBank are labeled with Accession number and original determination.
FIGURE 1b in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 1b. clustering of sequences representing Badis badis, a cluster of uncertain identification, and unidentified OTU from near Kaziranga. Excerpt from bPTP delimitation tree of species of the Badidae, based on coi sequences (Fig. S3). New sequences are labeled with tissue collection identifiers in NRM and DU. Sequences from GenBank are labeled with Accession number and original determination.
FIGURE 1a in Chameleonfishes in Bangladesh: hipshot taxonomy, sibling species, elusive species, and limits of species delimitation (Teleostei: Badidae)
FIGURE 1a. clustering of OTUs of Badis kyar, B. ferrarisi, B. corycaeus, B. assamensis, and GenBank samples identified as B. assamensis. Excerpt from bPTP delimitation tree of species of the Badidae, based on coi sequences (Fig. S3). New sequences are labeled with tissue collection identifiers in NRM. Sequences from GenBank are labeled with Accession number and original determination.
TEXT-FIGURE 4. Minutella cf. minuta (Cooper, 1981), "La Passe bateau" off the south-west coast of Mayotte Island. (1a–e) MNHN-IB-2017-173. a–d. Juvenile articulated specimen in dorsal, oblique lateral, posterior oblique views, and close-up of the posterior part of the shell (the protegulum is clearly limited by a step-like growth line and its surface is slightly granular; the rugideltidium is already well developed whereas the interarea remains reduced). e. Dorsal valve interior in plan view (early ju- venile stage in the ontogeny of the dorsal valve). (2a–c) MNHN-IB-2017-174: dorsal valve interior with well-preserved spicular canopies in plan and oblique posterior views, and close-up of the spicular canopy. (3) MNHN-IB-2017-175: articulated speci- men (young stage of growth). (4) MNHN-IB-2017-176: dorsal valve interior of a young specimen in plan view. in Recent thecideide brachiopods from a submarine cave in the Department of Mayotte (France), northern Mozambique Channel
TEXT-FIGURE 4. Minutella cf. minuta (Cooper, 1981), "La Passe bateau" off the south-west coast of Mayotte Island. (1a–e) MNHN-IB-2017-173. a–d. Juvenile articulated specimen in dorsal, oblique lateral, posterior oblique views, and close-up of the posterior part of the shell (the protegulum is clearly limited by a step-like growth line and its surface is slightly granular; the rugideltidium is already well developed whereas the interarea remains reduced). e. Dorsal valve interior in plan view (early ju- venile stage in the ontogeny of the dorsal valve). (2a–c) MNHN-IB-2017-174: dorsal valve interior with well-preserved spicular canopies in plan and oblique posterior views, and close-up of the spicular canopy. (3) MNHN-IB-2017-175: articulated speci- men (young stage of growth). (4) MNHN-IB-2017-176: dorsal valve interior of a young specimen in plan view.
Fig. 3 in Comparing Realized and Potential Distributions of the Species of Taurocerastinae (Coleoptera: Geotrupidae) to Examine the Relevance of Dispersal Limitations and Contemporary Environmental Factors
Fig. 3. Predicted potential distributions (red areas) when the conditions of the modeled environmental predictors are extrapolated to a global extent. A) Frickius variolosus, B) Taurocerastes patagonicus.
Fig. 1. Taurocerastinae.A in Comparing Realized and Potential Distributions of the Species of Taurocerastinae (Coleoptera: Geotrupidae) to Examine the Relevance of Dispersal Limitations and Contemporary Environmental Factors
Fig. 1. Taurocerastinae.A) Male Frickius costulatus, B) Male F. variolosus, C) Pair of Taurocerastes patagonicus. Photo A by Guillermo Moreno (used with permission); photos B and C by Mauricio GonzÁlez-Chang.
Fig. 2. A in Comparing Realized and Potential Distributions of the Species of Taurocerastinae (Coleoptera: Geotrupidae) to Examine the Relevance of Dispersal Limitations and Contemporary Environmental Factors
Fig. 2. A) Map showing the geographic occurrences of Frickius costulatus (two green points), F. variolosus (43 red points), and Taurocerastes patagonicus (37 blue points), B) Predicted distributional ranges for the three species, with the green area corresponding to the shared distributional range between the two Frickius species and the yellow area corresponding to the shared distributional area between F. variolosus and T. patagonicus.
Figure 1 in The limits of mtDNA analysis for determining the provenance of invasive species: a midwife toad example
Figure 1. Sampling of the common midwife toad (Alytes obstetricans). Samples from the Netherlands, Belgium and Germany were newly studied. The localities on the coast of the Netherlands (Meijendel and The Hague from top to bottom, enclosed by the pink dotted line) are introductions outside of the native range. Localities are color-coded according to the six major ND4 mtDNA clades, referred to as haplogroups by Gonçalves et al. (2015), to which they belong. Sampling details can be found in supplementary table S1.
Figure 3 in The limits of mtDNA analysis for determining the provenance of invasive species: a midwife toad example
Figure 3. Median Joining Network of 74 ND4 mtDNA haplotypes of the common midwife toad (Alytes obstetricans). Pie size reflects haplotype frequency and red numbers between parentheses reflect the number of substitutions (if greater than 1). The prefix 'Ao_H' is omitted from haplotype labels. Haplotype details can be found in supplementary table S1.
ScienceDex guides
Understand access before you commit
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.