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Figure 3 in New Data on Niphargidae (Amphipoda) from Northern Macedonia, Niphargus lowryi sp. nov.
Figure 3. Niphargus lowryi sp. nov., spring near Monastery St. Naum, Ohrid Lake coast, female 22.0 mm (holotype): (A–B) gnathopod 1, outer face; (C) corner of gnathopod 1 propodus, outer face [s = corner S-spine; l = lateral L-spines; r = subcorner R-spine; m = corner facial M-setae]; (D–E) gnathopod 2, outer face; (F) corner of gnathopod 2 propodus, outer face [s = corner S-spine; l = lateral L-spines; r = subcorner R-spine; m = corner facial M-setae].
Figure 4 in New Data on Niphargidae (Amphipoda) from Northern Macedonia, Niphargus lowryi sp. nov.
Figure 4. Niphargus lowryi sp. nov., spring near Monastery St. Naum, Ohrid Lake coast, female 22.0 mm (holotype): (A) maxilla 1; (B–C) pereopod 3; (D–E) pereopod 4; (F) epimeral plates 1–3; (G) telson.
Figure 2 in New Data on Niphargidae (Amphipoda) from Northern Macedonia, Niphargus lowryi sp. nov.
Figure 2. Niphargus lowryi sp. nov., spring near Monastery St. Naum, Ohrid Lake coast, female 22.0 mm (holotype): (A) labrum; (B) labium; (C) right mandible; (D) mandibular palp, inner face [b = facial B-setae; d = marginal D-setae; e = distal E-setae]; (E) mandibular palp distal article, outer face [a= facial A-setae]; (F) maxilla 2; (G) maxilliped; (H) maxilliped, distal part of palp; (I) pleopod 1 peduncle; (J) pleopod 2 peduncle; (K) pleopod 3 peduncle; (L) uropod 3.
Figure 1 in New Data on Niphargidae (Amphipoda) from Northern Macedonia, Niphargus lowryi sp. nov.
Figure 1. Niphargus lowryi sp. nov., spring near Monastery St. Naum, Ohrid Lake coast, female 22.0 mm (holotype): (A) head; (B) antenna 1; (C) accessory flagellum; (D) aesthetasc on antenna 1; (E) antenna 2; (F) urosome and uropods 1–2.
Appendices to the Roadmap for action for the project More Welfare: towards new risk assessment methodologies and harmonised animal welfare data in the EU
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CatVolc: A new database of geochemical and geochronological data of volcanic-related materials from the Catalan Volcanic Zone (Spain)
<p>The Catalan Volcanic Zone (CVZ) (NE Spain) consists of an intraplate alkaline volcanic zone associated with the opening of the Western Mediterranean and the development of the European Rift System. Volcanic activity in the CVZ started in the L’Empordà area (ca. > 12 - 8 Ma), extended to La Selva (7.9 - 1.7 Ma), and finally migrated to the Garrotxa Volcanic Field (< 0.7 - 0.01Ma). Despite the scientific interest in the CVZ since the early 19th century, certain aspects remain poorly constrained. These include a full understanding of the spatial and temporal evolution of the magma plumbing system and ascent mechanisms, as well as the chronology of volcanism across the CVZ. Addressing these unresolved questions requires geochemical, petrological, and geochronological data, which, in the case of the CVZ, are scattered and have never been integrated or analyzed within a unified framework. Here, we present the CatVolc (Catalan Volcanism) database, which compiles available geochemical and geochronological data of volcanic-related materials of the CVZ. For each sample, the CatVolc database lists general information about the sampling site, sample lithology, whole-rock analyses (including major and trace elements), isotopic ratios, mineral chemistry, and radiometric/thermoluminescence dating information, if available. A preliminary analysis of the information contained in the CatVolc database highlights the critical limitations of the current state of knowledge and allows suggesting potential future directions for volcanic-driven investigations in the CVZ. Additionally, the results obtained validate the CatVolc database as a key tool for comprehending the spatial and temporal evolution of the magmatic system(s) and volcanic activity in the CVZ, particularly in the Garrotxa Volcanic Field. This aspect is critical for advancing in the assessment of the volcanic hazards in the region and for gaining a comprehensive understanding of future volcanic activity.</p> <p>The current database version consists of three MS Excel files dedicated to primary magmatic rocks (<em>CatVolc_magmatic_rocks.xlsx</em>), xenoliths (<em>CatVolc_xenoliths.xlsx</em>) and radiometric/thermoluminescence dating information (<em>CatVolc_dating.xlsx</em>). Each MS Excel file is structured around a main table (<em>Samples_general_info</em>) containing general information (e.g., location, age, sampling site) of the listed samples, and a certain number of secondary tables. Secondary tables included in the MS Excel files for magmatic rocks and xenoliths report: (i) whole-rock geochemistry (<em>Major_elements</em> and <em>Trace_elements</em>); (ii) isotopic relations data (<em>Isotopic_relations</em>); and (iii) mineral and volcanic glass chemistry (<em>Amphibole</em><strong>, </strong><em>Feldspar</em><strong>, </strong><em>Felspathoid</em><strong>, </strong><em>Glass</em><strong>, </strong><em>Mica</em><strong>, </strong><em>Olivine</em><strong>, </strong><em>Pyroxene</em><strong>, </strong><em>Oxides</em><strong>, </strong><em>Serpentines</em><strong> </strong>and<strong> </strong><em>Sulphides</em><em>)</em>. In addition to the <em>Samples_general_info </em>table, the <em>CatVolc_dating.xlsx </em>also includes radiometric/thermoluminescence dating information (<em>Dating</em>). Finally, in all three Excel files, we have incorporated a table with consulted references (<em>References</em><em>) </em>and a glossary of the acronyms used for the parameters included in the main and secondary tables (<em>Codes</em>). </p> <p> </p>
Data from: A new trophic specialization buffers a top predator against climate-driven resource instability
<p>Intraspecific phenotypic variability is key to respond to environmental changes and anomalies. However, documenting the emergence of behavioral diversification in natural populations has remained elusive due to the difficulty of observing such phenomenon at the right time and place. Here, we investigated how the emergence of a new trophic strategy in a population subjected to high fluctuations in the availability of its main trophic resource (migrating songbirds) affected the breeding performance, population structure, and population fitness of a specialized color polymorphic predator, the Eleonora's falcon from the Canary Islands. Using long-term data (2007-2022), we found that the exploitation of an alternative prey (a local petrel species) was associated with the growth of a previously residual falcon colony. Pairs in this colony laid earlier and raised more fledglings than in the other established colonies. The specialization on petreles increased over time, independently of annual fluctuations in prey availability. Importantly, however, the positive effect of petrel consumption on productivity was stronger in years with lower food availability. This trophic diversification was further associated with the genetically-determined color morph, with dark individuals preying more frequently on petreles than pale ones, which might promote the long-term maintenance of genotypic and phenotypic diversity. We empirically demonstrate how the emergence of an alternative trophic strategy can buffer populations against harsh environmental fluctuations by stabilizing their productivity.</p>
Data from: A new mechanistic model for individual growth suggests upregulated maintenance costs when food is scarce in an insect
<p>In order to calibrate and evaluate a recently developed growth model, the Maintenance-Growth Model (MGM), for the case of growth under food restriction, empirical data for house crickets (<em>Acheta</em> <em>domesticus</em>) were collected and analysed. This data set contains data for individually reared crickets growing under two different regimes of controlled food limitation as well as data for food-limited cohorts of growing house crickets. The sets include temporal data for body mass and ingestion as well as age and size at maturation (imago emergence). The data for food-limited cohorts were collected prior to this study and parts of it have previously been analysed and presented in a publication on animal self-thinning. </p>
Figure 1 in Contribution to the knowledge of Parichoronyssus bakeri Morales-Malacara and Guerrero, 2007 (Mesostigmata: Macronyssidae): new locality and host-association records with additional molecular data
Figure 1 Light Microscopy images of the female Parichoronyssus bakeri. A – General view of the ventral idiosoma; B – General view of the dorsal idiosome; C – Close up of sternal shield; D – Close up of genital and anal shields; E – Gnathosoma and coxa of the Leg I, with the black arrow pointed out the spine-like projection; F – Close up of the dorsal shield. Scales: A and B 50µm, C-F 20µm.
Data for a publication: "A new promising material for biological applications: multi-level physical modification of AgNPs-decorated PEEK"
<p>The data set contains the data that were used within the article "A New Promising Material for Biological Applications: Multilevel Physical Modification of AgNP-Decorated PEEK" published in the journal Nanomaterials.</p> <p><strong>Versions:</strong></p> <p><strong>V1&2</strong>: The dataset contained AFM and UV VIS data.</p> <p><strong>V3</strong>: All the data used in the article are sorted in the file structure, which description is thoroughly described in the READ ME file. Additionally, the preprint DOI was added.</p> <p> </p> <p> </p>
Figs 10-11 in New faunistic and taxonomic data of the genus Pachyteria Audinet-Serville, 1883 (Coleoptera: Cermabycidae: Callichromatini)
Figs 10-11. Aedeagus of Pachyteria diversipes bouvieri Ritsema, 1896: 10 – dorsal view; 11 – lateral view. Scale bar = 1.0 mm.
Figs. 1-5 in A new species and new data of the genus Aristolebia Bates, 1892 (Coleoptera: Carabidae: Lebiini)
Figs. 1-5. Habitus and aedeagus of Aristolebia. 1 and 4 - A. saluki sp. n., Holotype; 2 - A. klimenkoi sp. n., Holotype; 3 and 5 - A. apicalis Baehr, 2010.
Data for iPyCLES v1.0: A New Isotope-Enabled Large-Eddy Simulator for Mixed-Phase Clouds
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Fig. 6 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 6. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model for 2041–2060 (all distribution data and bioclimatic variables; point-wise
Fig. 3 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 3. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model (all distribution data and bioclimatic variables for 1970–2000; point-wise
Fig. 5 in New data on distribution of Miramiola pusilla (Miram, 1927) (Orthoptera: Tettigoniidae
Fig. 5. Predicted probabilities of suitable conditions for Miramiola pusilla according the Maxent model for 2021–2040 (all distribution data and bioclimatic variables; point-wise
Figure 6 in Description of a new species of the genus Rana (Anura: Ranidae) from western Guizhou, China, integrating morphological and molecular genetic data
Figure 6. Variation of the live adult male paratype GZNU20220705001 of Rana zhijinensis Luo, Xiao & Zhou, sp. nov. A. Dorsolateral view; B. Dorsal view; C. Ventral view.
Figure 1 in Description of a new species of the genus Rana (Anura: Ranidae) from western Guizhou, China, integrating morphological and molecular genetic data
Figure 1. Sampling localities of Rana zhijinensis Luo, Xiao & Zhou, sp. nov., R. culaiensis, R. hanluica, and R. omeimontis in Guizhou Province, China. A. Guiguo Town, Zhijin County; B. Supu Town, Qianxi County; C. Zhujianshan Nature Reserve, Huangping County; D. Leigongshan National Nature Reserve, Leishan County.
Figure 2 in Description of a new species of the genus Rana (Anura: Ranidae) from western Guizhou, China, integrating morphological and molecular genetic data
Figure 2. Phylogenetic tree based on three mitochondrial genes and six nuclear genes. A. Maternal tree; B. Nuclear gene tree. In both phylogenetic tree, ultrafast bootstrap support (UFB) values from ML analyses/Bayesian posterior probabilities (BPP) from BI analyses are given beside nodes. Scale bars denote nucleotide substitutions per sites for mitochondrial and nuclear genes.
Figure 5 in Description of a new species of the genus Rana (Anura: Ranidae) from western Guizhou, China, integrating morphological and molecular genetic data
Figure 5. Morphological features of the live adult male holotype GZNU2018081606 of Rana zhijinensis Luo, Xiao & Zhou, sp. nov. A. Dorsolateral view; B. Dorsal view; C. Ventral view; D. Egg cluster; E. Ventral view of hand and dark gray-blackish nuptial pad; F. Ventral view of foot.
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.