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722 results for “use case”
Fig. 5 in Taxonomic Use of Genitalic Characters in Mexican Copris (Coleoptera: Scarabaeidae, Scarabaeinae): The Case of Copris klugi sierrensis Matthews and the C. armatus Species Complex
Fig. 5. Copris sierrensis. Raspula.
Fig. 3 in Taxonomic Use of Genitalic Characters in Mexican Copris (Coleoptera: Scarabaeidae, Scarabaeinae): The Case of Copris klugi sierrensis Matthews and the C. armatus Species Complex
Fig. 3. Copris klugi. Raspula.
Figure 5 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 5 Phlomoides henryi Y.Zhao & C.L.Xiang A habitat B plant with linear-tuberous roots C inflorescence D verticillaster E flowers F dissected flower G appendages at base of posterior filaments H fruiting calyces I dissected calyces J bracts K floral leaves L stem leaves. Photographs by Yue Zhao, except C by Li Chen.
Figure 4 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 4 SEM of both sides of leaves of Phlomoides henryi and related species A, BP. henryiC, DP. bracteosaE, FP. brevifloraG, HP. macrophyllaI, JP. nyalamensisK, LP. tibeticaM, NP. milingensisO, PP. rotataA, C, E, G, I, K, M, OSEM of adaxial leaves B, D, F, H, J, L, N, PSEM of abaxial leaves.
Figure 2 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 2 Different types of trichomes of PhlomoidesA short simple non-glandular trichomes (P. macrophylla) B short simple non-glandular trichomes (P. breviflora) C long simple non-glandular trichomes (P. henryi) D symmetrically non-glandular stellate (P. breviflora) E non-glandular stellate with central long branch (P. bracteosa) F bi- or trifurcate non-glandular stellate (P. nyalamensis) G sub-sessile/ sessile glandular trichomes (P. macrophylla) H simple glandular trichomes of (P. bracteosa) I branched glandular trichomes (P. breviflora).
Figure 1 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 1 Phylogeny of Phlomoides inferred by Bayesian Inference (BI), based on the combined plastid dataset cpDNA. Support values displayed on the branches follow the order BI-PP/ML-BS (" * " indicates PP = 1.00 or BS = 100%, "-" indicates incongruent relationship between BI and ML tree.
Figure 3 from: Zhao Y, Zhao F, Paton AJ, Xiao J-F, Chen Y-P, Xiang C-L (2024) Using scanning electron microscopy and molecular data to discover a new species from old herbarium collections: The case of Phlomoides henryi (Lamiaceae, Lamioideae). PhytoKeys 238: 127-146. https://doi.org/10.3897/phytokeys.238.117180
Figure 3 Photos of bracts, SEM of bracts of Phlomoides henryi and related species A, BP. henryiC, DP. bracteosaE, FP. brevifloraG, HP. macrophyllaI, JP. nyalamensisK, LP. tibeticaM, NP. milingensisO, PP. rotata. A, C, E, G, I, K, M, O photos of bracts B, D, F, H, J, L, N, PSEM of bracts.
Supplementary material 1 from: Matenaar D (2024) Application of extended depth of field 3D imagery to tackle the challenges of cryptic species: a use case in the genus Betiscoides Sjöstedt, 1924 (Orthoptera, Caelifera, Lentulidae) and its taxonomic implications. Evolutionary Systematics 8(1): 65-90. https://doi.org/10.3897/evolsyst.8.117735
Specimens collections sites and Genbank Acc. numbers
Analysis of The Use of Organic Materials as Subgrade Layer of Rigid Pavement (Case Study: Semarang – Demak Toll Road Section 1)
Open the record for dataset details and reuse information.
Aequitas WP7 Use Case HR2 Akkodis STEM data 1.0
<p>This dataset contains information about the hiring process conducted by Akkodis for job positions and candidates belonging to the STEM field. The data contains the curricula of candidates and the details of the job positions to which they were matched. The candidates and job positions are explicitly selected among the STEM field (including but not limited: computer science, engineering, physics, mathematics, chemistry, etc.). </p>
Spatial patterns of phylogenetic diversity and endemism in the Western Ghats, India: a case study using ancient predatory arthropods
<p><span><span><span>The Western Ghats (WG) mountain chain in peninsular India is a global biodiversity hotspot, one in which patterns of phylogenetic diversity and endemism remain to be documented across taxa. We used a well-characterized community of ancient soil predatory arthropods from the WG to understand diversity gradients, identify hotspots of endemism and conservation importance, and highlight poorly-studied areas with unique biodiversity. We compiled an occurrence dataset for 19 species of scolopendrid centipedes, which was used to predict areas of habitat suitability using bioclimatic and geomorphological variables in Maxent. We used predicted distributions and a time-calibrated species phylogeny to calculate taxonomic and phylogenetic indices of diversity, endemism and turnover. We observed a decreasing latitudinal gradient in taxonomic and phylogenetic diversity in the WG, which supports expectations from the latitudinal diversity gradient. The southern WG had the highest phylogenetic diversity and endemism, and was represented by lineages with long branch lengths as observed from relative phylogenetic diversity/endemism. These results indicate the persistence of lineages over evolutionary time in the southern WG and are consistent with predictions from the southern WG refuge hypothesis. The northern WG, despite having low phylogenetic diversity, had high values of phylogenetic endemism represented by distinct lineages as inferred from relative phylogenetic endemism. The distinct endemic lineages in this sub-region might be adapted to life in lateritic plateaus characterized by poor soil conditions and high seasonality. Sites across an important biogeographic break, the Palghat Gap, broadly grouped separately in comparisons of species turnover along the WG. The southern WG and Nilgiris, adjoining the Palghat Gap, harbour unique centipede communities, where the causal role of climate or dispersal barriers in shaping diversity remains to be investigated. Our results highlight the need to use phylogeny and distribution data while assessing diversity and endemism patterns in the WG.</span></span></span></p>
Supplementary material 1 from: Hatami R, Inglis G, Lane SE, Growcott A, Kluza D, Lubarsky C, Jones-Todd C, Seaward K, Robinson AP (2022) Modelling the likelihood of entry of marine non-indigenous species from internationally arriving vessels to maritime ports: a case study using New Zealand data. NeoBiota 72: 183-203. https://doi.org/10.3897/neobiota.72.77266
Supplementary materials
Analyzing Polyethylene Terephthalate Bottle Waste Technology Using Analytic Hierarchy Process for Developing Countries: A case Study from Indonesia
<p>PET bottle waste is easy to recycle because it is easy to separate, abundant, and competitively priced. Technologies for the treatment of PET bottle waste have been evaluated to date using life cycle assessment (LCA), but this does not take into account all the aspects that policy makers consider necessary to select an acceptable technology. Aspects such as society, economics, policies, and technical applicability need to be considered along with environment and resources consumption to complement the LCA results for PET bottle waste. These aspects were selected as criteria for the Analytical Hierarchy Process (AHP), and stakeholders were invited to make a comparison evaluation of the criteria and sub criteria. Academics were involved to compare the technology option. The results show that society is the highest priority because it is the main actor that ensures the application of the technology, and job creation is the most important indicator for the selection of the technology. After comparing open landfill, sanitary landfill, incineration with energy recovery, pelletizing, glycolysis, and hydrolysis for utilization of PET bottle waste, this study suggests pelletizing as the acceptable technology for Indonesia because pelletizing is supported by social aspects and creates more jobs. This is the first time that a single plastic fraction that is easy to collect and recycle has been studied with AHP. The results show that this type of plastic could also be reused in developing countries through mechanical recycling.</p>
Coded Segments - Use Cases for Software Analytics
<p>Supplementary material for SBES 2022: Coded segments resulting from data analysis.</p>
Statistical Data for The Impact of Chatbots using Concept Maps on Correction Outcomes–a Case Study of Programming Courses
<p>experiment learners' questionnaire result and test score</p>
Supplementary material 3 from: Molloy SW, Davis RA, Dunlop JA, van Etten EJB (2017) Applying surrogate species presences to correct sample bias in species distribution models: a case study using the Pilbara population of the Northern Quoll. Nature Conservation 18: 27-46. https://doi.org/10.3897/natureconservation.18.12235
Weighted mean SDMs for individual algorithms and evaluation statistics (biomod2) :
Supplementary material 2 from: Molloy SW, Davis RA, Dunlop JA, van Etten EJB (2017) Applying surrogate species presences to correct sample bias in species distribution models: a case study using the Pilbara population of the Northern Quoll. Nature Conservation 18: 27-46. https://doi.org/10.3897/natureconservation.18.12235
Full readout for the MaxEnt northern quoll SDM :
Supplementary material 1 from: Molloy SW, Davis RA, Dunlop JA, van Etten EJB (2017) Applying surrogate species presences to correct sample bias in species distribution models: a case study using the Pilbara population of the Northern Quoll. Nature Conservation 18: 27-46. https://doi.org/10.3897/natureconservation.18.12235
GIS data sets used in variable assessments and map of Pilbara vegetation systems :
Figure 1 from: Meier R, Ang Y, Wong L (2013) Using seemingly unnecessary illustrations to improve the diagnostic usefulness of descriptions in taxonomy–a case study on Perochaeta orientalis (Diptera, Sepsidae). ZooKeys 355: 9-27. https://doi.org/10.3897/zookeys.355.6013
Figure 1 - Key views and structures of Perochaeta orientalis, Male. A Habitus, lateral view B Pleural microtomensity pattern; (white = smooth, light grey = lightly microtomentose, dark grey = heavily microtomentose) C Rear tibia, with focus on osomterium D Basal section of wing showing microtrichosity pattern (white=smooth, light grey=with microtrichia) E Whole abdomen, ventral view F Sternite appendage G Hypopygium, dorsal view H Phallus, right, ventral and left views; red arrow indicates basal spiny flap. Scale bars = 0.5mm unless otherwise stated.
Figure 3 from: Meier R, Ang Y, Wong L (2013) Using seemingly unnecessary illustrations to improve the diagnostic usefulness of descriptions in taxonomy–a case study on Perochaeta orientalis (Diptera, Sepsidae). ZooKeys 355: 9-27. https://doi.org/10.3897/zookeys.355.6013
Figure 3 - Additional views for Perochaeta orientalis, Male (MA-MF) and Female (FA-FE). M and F prefixes refer to male and female specimen respectively. A Habitus, dorsal view (sans wings) B head and thorax, ventral view C Head capsule, anterior view D Head capsule, posterior view E Thorax, posterior view F (male only)–Rear tibia, dorsal view showing osmeterium. Scale bars = 0.5mm unless otherwise stated.
ScienceDex guides
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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.