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zenodo40/100

Figs 1–4 in The types of Lygistorrhinidae and Mycetophilidae (Diptera: Bibionomorpha) in the KwaZulu-Natal Museum, Pietermaritzburg, South Africa

Figs 1–4. (1) Lygistorrhina sanctaecatharinae Thompson, paratype "NMSA-Dip. 11308"; (2) Dinempheria enigmata Väisänen, holotype; (3) Dziedzickia peckorum Matile, paratype "NMSA-DIP 66399"; (4) Dziedzickia stuckenbergorum Matile, holotype. Scale bars = 1 mm.

opencc-by-4.0Dec 2012View details →
zenodo40/100

Figs 3, 4 in The megadrile fauna (Annelida: Oligochaeta) of Queen Elizabeth Park, South Africa: species composition and distribution within different vegetation types

Figs 3, 4. Tritogenia howickiana: (3) anterior part of the body, showing papillae and tubercula pubertatis ventrally; (4) dorsal dissection showing thickened septa. Abbreviations: Cl – clitellum, DB – double blood vessel, P – papillae of 15–17, S – septa 4/5–6/7, Tp – tubercula pubertatis,.

opencc-by-4.0Dec 2012View details →
zenodo40/100

Fig. 2 in Pupa menkeana Pfeiffer, 1853, type species of the speciose land snail genus Gulella Pfeiffer, 1856: correction of longstanding PLVLGHQWL¿FDWLRQ DQG GHVLJQDWLRQ RI QHRW\SH (Mollusca: Eupulmonata: Streptaxidae)

Fig. 2. (A, B) lectotype and paralectotype of Ennea adamsiana Pfeiffer, 1859 in 1854–1860, 'Port Natal, M.C. [Mus. Cuming]', length 8.45 and 8.1 mm (NHMUK 20110168); (C, D) syntypes of Ennea impervia Melvill & Ponsonby, 1896, 'Natal', length 8.8 and 8.75 mm (NHMUK 1903.3.11.85–86); (E) holotype of Ennea aurisleporis Melvill & Ponsonby, 1898, 'Natal', length 6.65 mm (NHMUK 1903.3.11.69); (F) holotype of Ennea socratica Melvill & Ponsonby, 1893, 'Pietermaritzburg', length 8.45 mm (NHMUK 1903.3.11.78); (G) Gulella menkeana, small inland form, Cumberland, Pietermaritzburg, length 7.2 mm (NMSA V9709); (H) G. menkeana, large form from coastal E. Cape, Port St Johns, length 9.24 mm (NMSA W561); (I) Pupa wahlbergi Krauss, 1848, probable paratype in SMNH, length 10.1 mm (SMNH-Type-2112); (J, K) P. wahlbergi Krauss, 1848, neotype, Durban Bluff, length 9.84 mm, diameter 4.92 mm (NMSA W7942/T2669); (L) holotype of Ennea formosa Melvill & Ponsonby, 1898, Pietermaritzburg, length 7.75 mm (NHMUK 1903.3.11.79).

opencc-by-4.0Dec 2011View details →
zenodo40/100

Figs 3, 4 in Primary types in the collection of molluscs in the KwaZulu-Natal Museum: Scaphopoda and Cephalopoda

Figs 3, 4. Sepia acuminata, SDUDOHFWRW\SHV 106$: () 2ΟΙ/7474, 4Ϭ.7î2Ι.2 PP>= Sepia hieronis (Robson, 1924)]; (4) 3200/T474, 48.6×21.7 mm.

opencc-by-4.0Dec 2011View details →
zenodo40/100

Figs 5–8 in Primary types in the collection of molluscs in the KwaZulu-Natal Museum: Scaphopoda and Cephalopoda

Figs 5–8. (5) Sepia confusa, syntype NMSA 3212/T475, 42.2×9.1 mm; (6) S. insignis, syntype NMSA 3210/T476, 18.4×5.8 mm; (7) S. incerta, syntype NMSA 3477/T477, 77.9×13.8 mm; (8) S. incerta, syntype NMSA 3207/T477, 35.1×9.8 mm.

opencc-by-4.0Dec 2011View details →
zenodo40/100

Figure 6 in Recovery of Dermatophagoides pteronyssinus (Acariformes: Astigmata: Pyroglyphidae) is influenced by vacuuming protocol, fabric type and the viability of dust mites

Figure 6 Scanning electron microscope for mites on fabrics: A – Cotton – LM (A1), DM (A2); B – Denim – LM (B1), DM (B2); C – Fleece - LM (C1), DM (C2).

opencc-by-4.0Jan 2023View details →
zenodo40/100

Figure 3 in Recovery of Dermatophagoides pteronyssinus (Acariformes: Astigmata: Pyroglyphidae) is influenced by vacuuming protocol, fabric type and the viability of dust mites

Figure 3 Mean number of LM (Live Mites), DM (Dead Mites) and EM (Euthanized Mites post fabric seeding) recovered according to each treatment applied irrespective of fabric type and duration of vacuuming. ∆ Mean value, and the central line in boxes represents median value of recovered mites.

opencc-by-4.0Jan 2023View details →
zenodo40/100

Figure 5 in Recovery of Dermatophagoides pteronyssinus (Acariformes: Astigmata: Pyroglyphidae) is influenced by vacuuming protocol, fabric type and the viability of dust mites

Figure 5 Scanning Electron Microscope image of the weave structure for fabrics used in this study. A – Cotton; B – Denim; C – Fleece.

opencc-by-4.0Jan 2023View details →
zenodo40/100

Figure 4 in Recovery of Dermatophagoides pteronyssinus (Acariformes: Astigmata: Pyroglyphidae) is influenced by vacuuming protocol, fabric type and the viability of dust mites

Figure 4 Mean number of LM (Live Mites), DM (Dead Mites) and EM (Euthanized Mites post fabric seeding) recovered from each fabric type according to duration of sampling irrespective of fabric type and vacuuming protocol applied. "*", "**" represent values for outliers (observations outside the interquartile range), ∆ Mean value. The central line in boxes represents median value of recovered mites.

opencc-by-4.0Jan 2023View details →
zenodo40/100

Figure 2 in Recovery of Dermatophagoides pteronyssinus (Acariformes: Astigmata: Pyroglyphidae) is influenced by vacuuming protocol, fabric type and the viability of dust mites

Figure 2 Mean number of LM (Live Mites), DM (Dead Mites) and EM (Mites euthanized post fabric seeding) recovered from each fabric type irrespective of the vacuuming protocol used and duration of vacuuming. "*", "**" represent values for outliers (outliers are observations outside the interquartile range), ∆ Mean value, and the central line in boxes represents median of recovered mites.

opencc-by-4.0Jan 2023View details →
dryad40/100

Data and code for: Building use-inspired species distribution models: using multiple data types to examine and improve model performance

<p>Species distribution models (SDMs) are becoming an important tool for marine conservation and management. Yet while there is an increasing diversity and volume of marine biodiversity data for training SDMs, little practical guidance is available on how to leverage distinct data types to build robust models. We explored the effect of different data types on the fit, performance and predictive ability of SDMs by comparing models trained with four data types for a heavily exploited pelagic fish, the blue shark (<em>Prionace</em> <em>glauca</em>), in the Northwest Atlantic: two fishery-dependent (conventional mark-recapture tags, fisheries observer records) and two fishery-independent (satellite-linked electronic tags, pop-up archival tags). We found that all four data types can result in robust models, but differences among spatial predictions highlighted the need to consider ecological realism in model selection and interpretation regardless of data type. Differences among models were primarily attributed to biases in how each data type, and the associated representation of absences, sampled the environment and summarized the resulting species distributions. Outputs from model ensembles and a model trained on all pooled data both proved effective for combining inferences across data types and provided more ecologically realistic predictions than individual models. Our results provide valuable guidance for practitioners developing SDMs. With increasing access to diverse data sources, future work should further develop truly integrative modeling approaches that can explicitly leverage strengths of individual data types while statistically accounting for limitations, such as sampling biases. </p>

opencc-zeroMay 2023View details →
zenodo40/100

Figure 1 in An additional larval type in the genus Chironomus - the yama-type

Figure 1. Photograph (left) and drawing (right) of the posterior prolegs and anal tubules of a yama-type larva.

opencc-by-4.0Dec 2016View details →
zenodo40/100

Distinct frequencies balance segregation with interaction between different memory types within a prefrontal circuit

<p>2023-05-30</p> <p>This archive holds the original data used to derive the results reported in the publication:<br> &#39;Distinct frequencies balance segregation with interaction between different memory types within a prefrontal circuit&#39;</p> <p>Authors: Martina Bracco, Tuomas P. Mutanen, Domenica Veniero, Gregor Thut &amp; Edwin M. Robertson<br> Corresponding Author: Edwin M. Robertson<br> Contact: edwin.robertson@glasgow.ac.uk</p> <p>Please refer to the License for the correct use of the data.&nbsp;<br> If the use of this data leads to any public dissemination, including (but not restricted to) scientific articles, conference presentations, and posters, please remember to cite the original article.</p> <p><br> <strong>General Description</strong></p> <p>The dataset is shared in BIDS format. To facilitate the upload of files to&nbsp;Zenodo, each subject folder was&nbsp;compressed separately. To ensure a valid bids structure of the dataset,&nbsp;extract the contents of each zip file and place them in the same directory as the other files from the dataset. By doing so, you will have all the necessary files in the correct structure for the BIDS format.</p> <p>Data type: raw TMS-EEG data organized in BIDS format, and epoched &plusmn;800 ms around the pulse.<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;preprocessed motor skill and word recall data organized in BIDS format (.tsv = data file; .json = data description).</p> <p>Key to Filenames: sub = Participant<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; ses-preLearning = Session 1 data folder<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; ses-postLearnng = Session 2 data folder<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; eeg = TMS-EEG data folder<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; beh = behaviral data folder</p> <p>Participants: 45 healthy participants (30 females, 23.9&plusmn;3.6 years; mean &plusmn; std)&nbsp;<br> &nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp;<br> Groups: Participants were randomly assigned to three different groups with different behavioural conditions:<br> &nbsp;&nbsp; &nbsp;- In the &#39;motorSkill&#39;-group, participants performed a sequential motor-skill task followed by a wordlist memory task.&nbsp;<br> &nbsp; &nbsp; &nbsp; &nbsp; (sub-01 to sub-15)<br> &nbsp;&nbsp; &nbsp;- In the &#39;wordRecall&#39;-group, &nbsp;participants performed a &nbsp;wordlist memory followed by a sequential task motor-skill task.<br> &nbsp; &nbsp;&nbsp;&nbsp; &nbsp;(sub-16 to sub-30)<br> &nbsp;&nbsp; &nbsp;- In the &#39;control&#39;-group, participants performed a random motor-skill task followed by a wordlist memory task.<br> &nbsp; &nbsp; &nbsp;&nbsp; &nbsp;(sub-31 to sub-45)</p> <p><strong>TMS-EEG data description</strong></p> <p>Stimulation sites: Right dorsolateral prefrontal cortex (rDLPFC).&nbsp;<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;Left primary motor cortex (lM1).</p> <p>Sessions: Session 1: TMS-EEG recordings before the behavioural tasks.<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Session 2: TMS-EEG recordings after the behavioural tasks.</p> <p>Number of TMS pulses: 126 pulses delivered to either DLPFC or M1 before, before and after behavioural tasks (a total of 252 pulses for Session 1 and Session 2, each).</p> <p>Inter-Stimulus Interval: 4-6 s (4.9&plusmn;0.6 s, mean &plusmn; std).</p> <p>TMS intensity: 80% of participants&#39; individual motor threshold.</p> <p>TMS machine: Magstim Rapid2, Magstim Company.</p> <p>Coil: figure-of-eight coil (Double 70-mm Alpha Coil).</p> <p>Number of channels: 62-channel EEG channels (AFz and TP9 are used as reference and ground, respectively)&nbsp;<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; + 1 FDI EMG channel<br> &nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;+ 1 electrode on the outer canthus of the left eye to monitor eye movements.</p> <p>Sampling rate: 5000 Hz.&nbsp;</p> <p>Voltage resolution: 0.1 uV.</p> <p>EEG system: TMS-EEG compatible BrainAmp (Brain Products).</p> <p>Noise masking during TMS-EEG recordings: Yes.&nbsp;</p> <p>&nbsp;</p> <p><strong>Memory tasks data description</strong></p> <p><br> <em>Motor skill task</em></p> <p>&#39;motorSkill&#39;-group (sub-01 to sub-15): TestSerial; averaged response time of the last 50 serial trials immediately after learning.<br> &nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; TestRandom; averaged response time for the 50 subsequent random trials immediately after learning.&nbsp;<br> &nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; RetestSerial; averaged response time for the last 50 serial trials 10h after learning.<br> &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;RetestRandom; averaged response time for the 50 subsequent random trials 10h after learning.</p> <p>&#39;wordRecall&#39;-group (sub-16 to sub-30): TestSerial; averaged response time for the last 50 serial trials immediately after learning.<br> &nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; TestRandom; averaged response time for the 50 subsequent random trials immediately after learning. &nbsp;&nbsp;&nbsp; &nbsp;</p> <p>&#39;control&#39;-group (sub-31 to sub-45): &nbsp; &nbsp;TestRandom; averaged response time of the last 100 random trials at testing.<br> &nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; RetestRandom; averaged response time of the last 100 random trials 10h after the tasks.</p> <p><em>Word recall task</em></p> <p>&#39;motorSkill&#39;-group (sub-01 to sub-15): Test; number of words recalled immediately after learning.</p> <p>&#39;wordRecall&#39;-group (sub-16 to sub-30): Test; number of words recalled immediately after learning.<br> &nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; Retest; number of words recalled 10h after learning. &nbsp;&nbsp;&nbsp; &nbsp;</p> <p>&#39;control&#39;-group (sub-31 to sub-45): &nbsp; &nbsp;Test; number of words recalled immediately after learning.</p>

opencc-by-4.0Jun 2023View details →
zenodo40/100

Source data for paper "Mapping disease regulatory circuits at cell-type resolution from single-cell multiomics data"

<p>Sample-paired scRNA-seq and scATAC-seq data collected from human&nbsp;peripheral blood mononuclear cells&nbsp;with&nbsp;<em>Staphylococcus aureus</em><em> </em>infection.&nbsp;ScATAC-seq data collected from human&nbsp;peripheral blood mononuclear cells&nbsp;with <em>COVID-19</em>&nbsp;infection.&nbsp;</p>

opencc-by-4.0Jun 2023View details →
zenodo40/100

UEyes: Understanding Visual Saliency across User Interface Types

<p>UEyes is a large eye-tracking-based dataset including 62 participants and 1,980 UI screenshots, covering four major UI types: webpage, desktop UI, mobile UI, and poster.&nbsp;</p> <p>Please cite the following paper:</p> <p>UEyes: Understanding Visual Saliency across User Interface Types</p> <p>https://dl.acm.org/doi/10.1145/3544548.3581096</p> <p>Yue Jiang, Luis A. Leiva, Hamed Rezazadegan Tavakoli, Paul R. B. Houssel, Julia Kylm&auml;l&auml;, and Antti Oulasvirta. 2023. UEyes: Understanding Visual Saliency across User Interface Types. In Proceedings of the 2023 CHI Conference on Human Factors in Computing Systems (CHI &#39;23). Association for Computing Machinery, New York, NY, USA, Article 285, 1&ndash;21. https://doi.org/10.1145/3544548.3581096</p>

opencc-by-4.0Jun 2023View details →
zenodo40/100

Fig. 5. Data labels. A. Xylocopamoerens Perty, 1833 in The primary types of some species of Centris bees described by European entomologists in the 18 and 20 centuries (Hymenoptera: Apidae)

Fig. 5. Data labels. A. Xylocopamoerens Perty, 1833 (lectotype ♀). B. Xylocopaxanthocnemis Perty, 1833 (lectotype ♂).

opencc-by-4.0Mar 2023View details →
zenodo40/100

Fig. 1. Data labels. A. Centris debilis Dominique, 1898 in The primary types of some species of Centris bees described by European entomologists in the 18 and 20 centuries (Hymenoptera: Apidae)

Fig. 1. Data labels. A. Centris debilis Dominique, 1898 (lectotype ♂). B. Centris dominiquella Dominique, 1898 (lectotype ♀).

opencc-by-4.0Mar 2023View details →
zenodo40/100

Fig 2. Data labels. A. Centris zonalis Dominique, 1898 in The primary types of some species of Centris bees described by European entomologists in the 18 and 20 centuries (Hymenoptera: Apidae)

Fig 2. Data labels. A. Centris zonalis Dominique, 1898 (lectotype ♀). B. Centris lyngbyei Jensen- Haarup, 1908 (lectotype ♂).

opencc-by-4.0Mar 2023View details →
zenodo40/100

Fig. 4. Data labels. A in The primary types of some species of Centris bees described by European entomologists in the 18 and 20 centuries (Hymenoptera: Apidae)

Fig. 4. Data labels. A. Centrisrhodophthalma Pérez, 1911 (lectotype ♀). B. Centristransversa Pérez, 1905 (lectotype ♀).

opencc-by-4.0Mar 2023View details →
zenodo40/100

Alert Type Frequency Assessment of Open-Source Static Analysis Tools and Codebases

<p>This includes all data needed to replicate and validate our frequency analysis of static analysis (SA) alerts produced using open-source SA tools on several OSS codebases. It includes instructions how to get and run the SA tools, a Dockerfile to conveniently get and use the SA tools, raw SA tool output, some python scripts to parse that output, parsed SA data and aggregate analyses, and SA data augmented with CERT coding rule and CWE data. &nbsp;</p> <p>The SA tools used:</p> <ul> <li>clang-tidy version 15.07&nbsp; &nbsp;</li> <li>cppcheck version 2.9 &nbsp;&nbsp;</li> <li>CERT Rosecheckers &nbsp;&nbsp;</li> </ul> <p>The codebases analyzed:</p> <ul> <li>zeek version 5.1.1</li> <li>git version 2.39.0</li> <li>dos2unix version 7.4.3</li> </ul>

opencc-by-4.0Jun 2023View details →

ScienceDex guides

Understand access before you commit

These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

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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