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zenodo40/100

Handling of Personal Data by Smart Home Equipment: an Exploratory Analysis in the Context of LGPD

<p>This dataset provides data about an exploratory research that analyzed the Privacy and Security Policies and the Instruction Manuals of 59 home automation equipment for Smart Home in order to verify which personal data was handled and how these documents were providing information about processes performed in personal data. The analysis was conducted with a quantitative approach followed by a qualitative analysis, using content analysis.</p>

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

Fig. 5 in Parasitic gastropod bioerosion trace fossil on Cenomanian oysters from Le Mans, France and its ichnologic and taphonomic context

Fig. 5. Parasitic gastropod bioerosion and perforation trace Loxolenichnus stellatocinctus igen. et isp. nov., MHNLM 2015.2.244, holotype, Marnes à Pycnodonte biauriculata Formation, Upper Cenomanian, Lycée Bellevue earthmoving works, Le Mans, Sarthe Department, France; on LV of Rhynchostreon suborbiculatum (Lamarck, 1801). A. Entire LV shell with the arrow showing the perforation. B. LV (viewed from inside), the arrow shows the opening of the perforation on the inner side of the shell, diascopic illumination. Outer (C) and inner (D) sides of the shell, close-ups of the perforation, the dashed line delimitates approximately the course of the perforation through the shell, diascopic illumination. E. Positive X-ray print of the perforation.

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

Fig. 6 in Parasitic gastropod bioerosion trace fossil on Cenomanian oysters from Le Mans, France and its ichnologic and taphonomic context

Fig. 6. Parasitic gastropod bioerosion trace Loxolenichnus stellatocinctus igen. et isp. nov., MHNLM 2015.2.346 and MHNLM 2015.2.347, paratypes; lower Campanian Inoceramus lingua–Goniotheuthis quadrata Zone, quarry near Höver, Germany. A. Outer side of an oyster valve, accommodating two specimens of L. stellatocinctus (arrows). B. Close-up of the two specimens and the multiple perforations. C. Inner side of the oyster valve showing two of the perforations reaching the adductor muscle pad. Outer (D) and inner (E) sides of an oyster valve with a marginal L. stellatocinctus. F. Close-up of D, note the two concentric stellate rims and the marginal notch.

opencc-by-4.0Nov 2016View details →
dryad40/100

Data from: Response to MHC-based olfactory cues in a mate choice context in two species of darter (Percidae: Etheostoma)

<p>Mate choice is hypothesized to play an important role in maintaining high diversity at major histocompatibility complex (MHC) genes in vertebrates. Many studies have revealed that females across taxa prefer the scent of males with MHC genotypes different to their own. In this study we tested the "opposites-attract" hypothesis in two species of darter with known differences in female criteria used in mate choice: in the fantail darters (a paternal-care species), females prefer males with visual traits related to nest guarding and egg tending, while in rainbow darters (not a paternal-care species) female mate choice criteria are unknown. In dichotomous mate-choice trials, we presented females of both species with the scents of conspecific males with MHC class IIb genotypes that were either similar or dissimilar to that of the focal female. We evaluated the proportion of time each female spent with each male and calculated the average strength of female preference for both species. Female fantail darters demonstrated a preference for the scent of males with similar (rather than dissimilar) MHC genotypes, but this result was not statistically significant. Rainbow darter females showed no preference for the scent of males with similar or dissimilar MHC genotypes. Our results do not support the "opposites-attract" hypothesis in darters.</p>

opencc-zeroFeb 2024View details →
zenodo40/100

Figure 12 in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 12. Juvenile Stage III of Procambarus virginalis. (A) Antenna 1, dorsal view; (B) antennal scale, dorsal view; (C) flagellum of antenna 2, dorsal view; (D) mandible, view of inside of mouth; (E) maxilla 1, oral view; (F) maxilla 2, oral view; (G) first maxilliped, oral view; (H) second maxilliped, oral view; (I) third maxilliped, oral view; (J) pleopod. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 15. Juvenile Stage II in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 15. Juvenile Stage II of Cambaroides japonicus. (A) Habitus, lateral view; (B) eses and rostrum, dorsal view; (C) tail fan, dorsal view; (D) posterior edge of tail fan; (E–I) pereiopods 1–5, dorsal or lateral view; (J–N) distal segments of pereiopods 1–5, dorsal or lateral view. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 11 in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 11. Juvenile Stage III of Procambarus virginalis. (A) Habitus, lateral view; (B) eses and rostrum, dorsal view; (C) tail fan, dorsal view; (D–H) pereiopods 1–5, dorsal or lateral view; (I–M) distal segments of pereiopods 1–5, dorsal or lateral view. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 18 in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 18. Juvenile Stage III of Cambaroides japonicus. (A) Antenna 1, dorsal view; (B) antennal scale, dorsal view; (C) antenna 2, dorsal view; (D) mandible, view of inside of mouth; (E) maxilla 1, oral view; (F) maxilla 2, oral view; (G) first maxilliped, oral view; (H) second maxilliped, oral view; (I) third maxilliped, oral view; (J) pleopod. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 10. Juvenile Stage II in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 10. Juvenile Stage II of Procambarus virginalis. (A) Antenna 1, dorsal view; (B) antennal scale, dorsal view; (C) flagellum of antenna 2, dorsal view; (D) mandible, view of inside of mouth; (E) maxilla 1, oral view; (F) maxilla 2, oral view; (G) first maxilliped, oral view; (H) second maxilliped, oral view; (I) third maxilliped, oral view; (J) pleopod. Scale bar: 0.25 mm.

opencc-by-4.0Feb 2022View details →
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Figure 9. Juvenile Stage II in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 9. Juvenile Stage II of Procambarus virginalis. (A) Habitus, lateral view; (B) eses and rostrum, dorsal view; (C) tail fan, dorsal view; (D–H) pereiopods 1–5, dorsal or lateral view; (I–M) distal segments of pereiopods 1–5, dorsal or lateral view. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 16. Juvenile Stage II in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 16. Juvenile Stage II of Cambaroides japonicus. (A) Antenna 1, dorsal view; (B) antennal scale, dorsal view; (C) antenna 2, dorsal view; (D) mandible, view of inside of mouth; (E) maxilla 1, oral view; (F) maxilla 2, oral view; (G) first maxilliped, oral view; (H) second maxilliped, oral view; (I) third maxilliped, oral view; (J) pleopod. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 13. Juvenile Stage I in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 13. Juvenile Stage I of Cambaroides japonicus. (A) Habitus, lateral view; (B) eses and rostrum, dorsal view; (C) tail fan and telson thread, dorsal view; (D) posterior edge of the telson and telson thread; (E–I), pereiopods 1–5, dorsal or lateral view; (J–N) distal segments of pereiopods 1–5, dorsal or lateral view. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 17 in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 17. Juvenile Stage III of Cambaroides japonicus. (A) Habitus, lateral view; (B) eses and rostrum, dorsal view; (C) tail fan, dorsal view; (D) posterior edge of tail fan; (E–I) pereiopods 1–5, dorsal or lateral view; (J–N) distal segments of pereiopods 1–5, dorsal or lateral view. Scale bars: 0.5 mm in A–C, 0.25 mm in D–M.

opencc-by-4.0Feb 2022View details →
zenodo40/100

Figure 7. Juvenile Stage I in Postembryonic development in freshwater crayfish (Decapoda: Astacidea) in an evolutionary context

Figure 7. Juvenile Stage I of Procambarus virginalis. (A) Habitus, lateral view; (B) eses and rostrum, dorsal view; (C) tail fan and telson thread, dorsal view; (D) posterior edge of the tail fan and telson thread; (E–I), pereiopods 1–5, dorsal or lateral view; (J–N) distal segments of pereiopods 1–5, dorsal or lateral view. Scale bars: 0.25 mm.

opencc-by-4.0Feb 2022View details →
dryad40/100

Context-dependent multimodal behaviour in a coral reef fish: Stage 1 & 2 total duration and count data in behaviour trials

<p>Animals are expected to respond flexibly to changing circumstances, with multimodal signalling providing potential plasticity in social interactions. Whilst numerous studies have documented context-dependent behavioural trade-offs in terrestrial species, far less work has considered such decision-making in fish, especially in natural conditions. Coral reef ecosystems host 25% of all known marine species, making them hotbeds of competition and predation. We conducted experiments with wild Ambon damselfish (<em>Pomacentrus amboinensis)</em> to investigate context-dependent responses to a conspecific intruder; specifically, how nest defence is influenced by an elevated predation risk. We found that nest-defending male Ambon damselfish responded aggressively to a conspecific intruder, spending less time sheltering and more time interacting, as well as signalling both visually and acoustically. In the presence of a model predator compared to a model herbivore, males spent less time interacting with the intruder, with a tendency towards reduced investment in visual displays compensated for by an increase in acoustic signalling instead. We therefore provide ecologically valid evidence that the context experienced by an individual can affect its behavioural responses and multimodal displays towards conspecific threats.</p>

opencc-zeroMar 2024View details →
zenodo40/100

Image repository for "Towards advancing Translators' Guidance for Organisations Tackling Innovation Challenges in Manufacturing within an Industry 5.0 context"

<p>The files on this trusted repository&nbsp; are provided by the authors of the manuscript with the title &ldquo;Towards advancing Translators&rsquo; Guidance for Organisations Tackling Innovation Challenges in Manufacturing within an Industry 5.0 context&rdquo; that was received by the MDPI journal Sustainability (ISSN 2071-1050) on 29 January 2024, got the manuscript ID sustainability-2872279, and is intended to become part of the special issue &ldquo;Sustainable Materials, Manufacturing and Design&rdquo; accessible under the link <a href="https://www.mdpi.com/journal/sustainability/special_issues/Sus_materials_manufacturing_design">https://www.mdpi.com/journal/sustainability/special_issues/Sus_materials_manufacturing_design</a>.</p> <p>The authors Paul-Ludwig Michael Noeske, Alexandra Simperler, Welchy Leite Cavalcanti, Vinicius Carrillo Beber, Brendon Weager, Tasmin Alliott, Peter Schiffels, and Gerhard Goldbeck aim at facilitating common access to the files representing high-resolution microscopy images (corresponding to the light microscopy (LM) and scanning electron microscopy (SEM) images shown in Figure 9 and Figure 12 in the manuscript or complementing them) given in .jpg and .tif format, respectively. Moreover, this repository comprises a .csv file containing the data points underlying the values presented in Table A1 of this manuscript and their description. The authors indicate here that following the sixth step of the translation process in materials modelling the translator may provide these data in this presentation that is adapted to the process-centric perspective required by representatives of an enterprise manufacturing prepregs and to their background knowledge disclosed to the translator beforehand.&ldquo;</p>

opencc-by-4.0Mar 2024View details →
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Fig. 1. Geological and geographic context. A in New bioerosion traces in rhynchosaur bones from the Upper Triassic of Brazil and the oldest occurrence of the ichnogenera Osteocallis and Amphifaoichnus

Fig. 1. Geological and geographic context. A. Location of the Paraná Basin in Brazil. B. Limits of the Triassic rocks of Rosário do Sul Group and the Triassic rocks of Paraná Basin in Rio Grande do Sul state. C. Location of the Buriol Site, locality of UFRGS-PV-1581-T, and nearby Predebon and Janner sites. D. Chrono-, lito-, and biostratigraphy of southern Brazilian Triassic (modified from Schultz et al. 2020). Arrow indicates stratigraphical position of UFRGS-PV-1581-T; * refers to absolute ages from Langer et al. (2018); ** refers to absolute ages from Philipp et al. (2018).

opencc-by-4.0Jan 2024View details →
zenodo40/100

Figures 9–17 in Gelidiella papillosa sp. nov. (Gelidiellaceae, Rhodophyta) from Veracruz, Mexico, in the context of the worldwide distribution of G. acerosa

Figures 9–17: Gelidiella papillosa sp. nov. (9) UAMIZ-1438. Detail of main axis and branchlets showing darkened tips. Scale bar = 3 mm. (10) UAMIZ-1433. Fresh specimen showing detail of basal region of main axis with papillose bumps (arrows). Inset, enlargement of a bump. Scale bar = 1.5 mm. (11) UAMIZ-1432. Cross section of basal portion of main axis showing a papilla with depressed apex (arrow). Scale bar = 130 µm. (12) UAMIZ-1436. Cross section of basal portion of main axis showing development of papilla without evident apical cell, with blunt apex. Scale bar = 66 μm. (13) UAMIZ-1437. Cross section of main axis showing outer cortical cells (arrowheads), inner cortical cells (blue arrows) and medullary cells (black arrows). Scale bar = 15 µm. (14) UAMIZ-1433. Detail of fertile branch showing swollen stichidia at apices of branchlets (arrows). Scale bar = 1 mm. (15) UAMIZ-1432. Cross section through middle portion of fertile branchlet showing arrangement of tetrasporangia (arrows). Scale bar = 110 µm. (16) UAMIZ-1433. Cross section of fertile branchlet showing immature tetrasporangia arising from inner cortical cells (arrows) and premature development of tetrasporangia (arrowheads). Scale bar = 30 µm. (17) UAMIZ-1432. Cross section through middle portion of fertile branchlet showing mature tetrasporangia. Scale bar = 30 µm.

opencc-by-4.0Oct 2023View details →
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Figures 3–8 in Gelidiella papillosa sp. nov. (Gelidiellaceae, Rhodophyta) from Veracruz, Mexico, in the context of the worldwide distribution of G. acerosa

Figures 3–8: Gelidiella papillosa sp. nov. (3) Holotype specimen, tetrasporic plant. UAMIZ-1432. Scale bar = 1 cm. (4) UAMIZ-1435. Fresh specimen of tetrasporic plant showing general appearance of the thallus. Scale bar = 5 mm. (5) UAMIZ-1437. Vegetative plant showing branching pattern in erect axes arising from a decumbent stolon. Scale bar = 1 cm. (6) UAMIZ-1437. Cross section through middle part of an erect axis. Scale bar = 130 µm. (7) UAMIZ-1432. Tip of branchlet showing numerous superficial cortical hairs (arrows). Scale bar = 700 µm. (8) UAMIZ-1432. Detail of young branchlet showing apical cell (arrow). Scale bar = 200 µm.

opencc-by-4.0Oct 2023View details →
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Figure 2 in Gelidiella papillosa sp. nov. (Gelidiellaceae, Rhodophyta) from Veracruz, Mexico, in the context of the worldwide distribution of G. acerosa

Figure 2: Bayesian inference (BI) topology based on rbcL sequence data. BI values (left) followed by maximum likelihood (ML) bootstrap (right) on branches. Asterisks indicate full support (ML = 100 %, BI = 1.0 %), hyphens indicate values below 70 %. Vertical bars on right indicate results of three species delimitation methods: automatic barcoding gap detection (ABGD), the Bayesian variant of Poisson trees processes model (bPTP)and the general-mixed-Yule-coalescent (GMYC). SCI and SCII indicate the two subclades (subclade I and subclade II), G1-G6 indicates the genetic groups within Gelidiella acerosa. Sequences generated in this study are in bold type. S.P.S. = substitutions per site.

opencc-by-4.0Oct 2023View 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