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Fig. 2 in Clarifications and new data on the distribution of Cacyreus marshalli Butler, 1898 in Bulgaria (Insecta, Lepidoptera, Lycaenidae)
Fig. 2. Right: Adult Cacyreus marshalli Butler, 1898 from NW Bulgaria: Vinarovo, 28.12.2017; left and center: Pupal exuvia of Cacyreus marshalli Butler, 1898 on a Pelargonium leaf, same locality. Photos: Tsvetomir Tsvetanov.
Data for: The rise of New Guinea and the fall of Neogene global temperatures
<p class="MsoPlainText">This dataset contains the output files of numerical simulations of the model GEOCLIM-DynSoil-steady-state, which were conducted for the study "The rise of New Guinea and the fall of Neogene global temperatures". Those outputs are modelled fields of erosion rate, silicate weathering flux, regolith thickness and primary phase depletion, on the island of New Guinea, at 30-minute resolution, and for 19 time slices from 15 Ma to present-day. This dataset also contains additional Python scripts for generating inputs of the model (namely, slope field) and for projecting the 2D New Guinea erosion field on the 1D transect highlighted in the abovementioned study.</p>
Data for: Range reshuffling: climate change, invasive species, and the case of Nothofagus forests in Aotearoa New Zealand
<p class="MsoNormal"><strong>Aim: </strong></p> <p class="MsoNormal">The impact of climate change on forest biodiversity and ecosystem services will be partly determined by the relative fortunes of invasive and native forest trees under future conditions. Aotearoa New Zealand has high conservation value native forests and one of the world's worst invasive tree problems. We assess the relative effects of habitat redistribution on native <em>Nothofagus </em>and invasive conifer (Pinaceae) species in New Zealand as a case study on the compounding impacts of climate change and tree invasions.</p> <p class="MsoNormal"><strong>Location: </strong></p> <p class="MsoNormal">Aotearoa New Zealand</p> <p class="MsoNormal"><strong>Methods: </strong></p> <p class="MsoNormal">We use species distribution models (SDMs) to predict the current and future distribution of habitat for five native <em>Nothofagus</em> species and 13 invasive conifer species under two 2070 climate scenarios. We calculate habitat loss/gain for all species and examine overlap between the invasive and native species now and in the future. </p> <p class="MsoNormal"><strong>Results: </strong></p> <p class="MsoNormal">Most species will lose habitat overall. The native species saw large changes in the distribution of habitat with extensive losses in North Island and gains mostly in South Island. Concerningly, we found that most new habitat for <em>Nothofagus </em>was also suitable for at least one invasive species. However, there were refugia for the native species in the wetter parts of the climate space.</p> <p class="MsoNormal"><strong>Main conclusion:</strong></p> <p class="MsoNormal">If the predicted changes in habitat distribution translate to shifts in forest distribution it would cause widespread ecological disruption. We discuss how acclimation, adaptation and biotic interactions may delay some changes. But we also highlight how the poor migration and establishment capacity of native <em>Nothofagus</em> and the competitive ability of invasive conifers will be a persistent conservation challenge in areas of both new habitat and forest retreat. Pinaceae are problematic invaders globally, and our results highlight that control of invasions and active native forest restoration will likely be key to managing forest biodiversity under future climates.</p>
Microsatellite data of the paper "A putatively new ant species from the Cataglyphis cursor group displays low levels of polyandry with standard sexual reproduction"
<p>Fifty colonies of the ant Cataglyphis cursor were sampled at their nest entrance in two localities separated by 79km in the plain of Avila, west of Madrid, in July 2015 for Salobralejo (27 colonies) and in April 2014 for Castrillo de Guareña (23 colonies). Only workers near the nest entrance were collected. In Salobralejo, we also collected nine gynes at the nest entrance in three colonies. After collection, the individuals were preserved in 95% Ethanol (with 5% Tris-EDTA). From the 50 colonies sampled, we genotyped a single worker per colony for 37 colonies (Table S1). For the other 13 colonies, 114 workers were collected and genotyped to assess the colony genetic structure (86 workers from nine colonies in Salobralejo and 28 workers from four colonies in Castrillo). We also genotyped the nine gynes found in three colonies in Salobralejo. A total of 160 individuals were screened for thirteen microsatellite loci used by Eyer et al. (2023) and two supplementary loci (L76 and L3653) were amplified. The L26 locus was excluded because of amplification failures in nine individuals (18% of samples) and a highly significant Hardy-Weinberg disequilibrium (<em>P</em> < 00001 for both sites). </p> <p>The file contain the locality (Salobralejo or Castrillo), the colony number and individual identification number (code), the caste (worker or gyne). For each locus, the two alleles are provided and characterised by their size. </p>
Data from: A review of the glacial environment arthropod trace fossils Umfolozia and Warvichnium with the description of new ichnotaxa
<p><span>Trace fossils are important records of the presence and behaviour of animals in the past, especially in deposits where few body fossils are preserved. They tend to provide the main palaeobiological </span>record for past glacial environments and are thus very important for understanding the ecology of these palaeoenvironments. Two ichnogenera are common from past glacial environments: <em>Umfolozia</em> and <em>Warvichnium</em>. Both <em>Umfolozia</em> and <em>Warvichnium</em> are attributed to arthropods, and the former occurs across the Late Palaeozoic Ice Age (LPIA) and the latter occurs during both the LPIA and the Quaternary glacial event. Here, we review the stratigraphic record, ichnotaxonomy, palaeoecology, palaeoenvironments, and likely tracemakers of these two ichnogenera. In addition to assessing morphological ichnotaxobases, we use multivariate morphometric analysis and inferential statistical tests to support our ichnotaxonomic revisions. The diagnosis of <em>Umfolozia</em> is revised, with the description of a new ichnospecies, <em>Umfolozia</em> <em>terere</em> isp. nov., and the emendation of the previously named <em>Umfolozia</em> <em>riojana</em> (formerly <em>Umfolozia</em> <em>longula</em>) nom. rev. emend. We revised Warvichnium, maintaining the original <em>Warvichnium</em> <em>ulbrichi</em>, and allocating two morphologies to the ichnogenus <em>Irichnus</em>: <em>Irichnus</em> <em>saltatorius</em> and <em>I. paripinnatus</em> isp. nov. These trace fossils record several behaviours, and have implications for palaeoenvironmental interpretations and the evolution of invertebrate ecosystems. Using <em>Umfolozia</em> and <em>Warvichnium</em> as case studies, we demonstrate the application of morphometric analysis in ichnotaxonomy and highlight this as a tool that may be applied to other trace-fossil groups.</p>
Figs. 1–5 in New data on distribution of winter insects (Mecoptera: Boreidae; Diptera: Limoniidae) in Western Siberia
Figs. 1–5. Winter insects of Western Siberia. 1, 2 – Boreus westwoodi: 1 – ♀; 2 – ♂; 3 – Chionea araneoides, ♀; 4, 5 – Chionea crassipes crassipes: 4 – ♀; 5 – ♂.
Data: "Happy new ears: rapid adaptation to novel spectral cues in vertical sound localization."
<p>Data related to the manuscript entitled: "Happy new ears: rapid adaptation to novel spectral cues in vertical sound localization.". For more information, read the README file.</p>
FIG. 22 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 22. — Distribution map of Ctenorillo ferrarai Campos-Filho, Araujo & Taiti, 2014. Abbreviations: PA, state of Pará; SL, Serra Leste; TO, state of Tocantins.
FIG. 20 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 20. — Trichorhina amplitelson Campos-Filho, Carpio-Díaz & Borja-Arrieta, n. sp.: A, female paratype, LES 27990 uropod; B-I, male paratype, LES 27990: pereopod 1 (B); pereopod 7 (C); genital papilla (D); pleopod 1 (E); pleopod 2 (F); pleopod 3 exopod (G); pleopod 4 exopod (H); pleopod 5 exopod (I).
FIG. 7 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 7. — Caraiboscia jabutiensis Campos-Filho, Taiti & Bichuette, n. sp., A, female paratype, LES 27986: uropod; B-H, male paratype, LES 27986: pereopod 1 (B); pereopod 7 (C); genital papila (D); pleopod 1 (E); pleopod 2 (F); pleopod 3 exopod (G); pleopod 4 exopod (H).
FIG. 6 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 6. — Caraiboscia jabutiensis Campos-Filho, Taiti & Bichuette, n. sp., female paratype, LES 27986: A, dorsal habitus; B, scale-seta; C, noduli laterales d/c coordinates; D, noduli laterales b/c coordinates; E, cephalon, dorsal view; F, cephalon, frontal view; G, pleonite 5 and telson; H, antennula; I, antenna; J, left mandible; K, right mandible; L, maxillula; M, maxilla; N, maxilliped. Scale bar: A, 1 mm.
FIG. 26 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 26. — Diploexochus carrapicho Campos-Filho, López-Orozco & Taiti, n. sp.: A, B, female paratype LES 28001: uropod frontal view (A); uropod, ventral view (B), C-H, male holotype, LES 28000: pereopod 7 (C); pleopod 1 (D); pleopod 2 (E); pleopod 3 exopod (F); pleopod 4 exopod (G); pleopod 5 exopod (H).
FIG. 41 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 41. — Venezillo dioi Campos-Filho, Araujo & Taiti, n. sp., male holotype, LES 28010: A, lateral habitus; B, scale-seta; C, cephalon and pereonites 1 and 2, frontal view; D, cephalon, back view; E, cephalon, frontal view; F, cephalon, dorsal view; G, pereonite 1 epimeron, dorsal view; H, pereonite 1 epimeron, ventral view; I, pereonite 2 epimeron, dorsal view; J, pereonite 2 epimeron, ventral view; K, pleonites 3-5, telson, and uropods, dorsal view; L, telson; M, antennula; N, antenna. Scale bar: A, 1 mm.
FIG. 47 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 47. — Venezillo muriloi Campos-Filho, Sfenthourakis & Taiti, n. sp., male holotype, LES 28048: A, left mandible; B, right mandible; C, maxillula; D, maxilla; E, maxilliped.
FIG. 42 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 42. — Venezillo dioi Campos-Filho, Araujo & Taiti, n. sp., male holotype, LES 28010: A, left mandible; B, right mandible; C, maxillula; D, maxilla; E, maxilliped.
FIG. 17 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 17. — Circoniscus caeruleus Campos-Filho, Sfenthourakis & Bichuette, n. sp., male holotype, LES 27987: A, left mandible; B, right mandible; C, maxillula; D, maxilla; E, maxilliped.
FIG. 35 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 35. — Venezillo moreirai Campos-Filho, Carpio-Díaz & Bichuette, n. sp., female paratype, LES 28007: A, lateral habitus; B, scale-seta; C, cephalon and pereonites 1-3, lateral view; D, cephalon, back view; E, cephalon and pereonites 1 and 2, frontal view; F, cephalon and pereonite 1 epimera, dorsal view; G, pereonite 1 epimeron, dorsal view; H, pereonite 1 epimeron, ventral view; I, pereonite 2 epimeron, dorsal view; J, pereonite 2 epimeron, ventral view; K, pleonites 3-5, telson, and uropods, dorsal view; L, pleonites 3-5 epimera, telson, and uropods, ventral view; M, antenulla; N, antenna. Scale bar: A, 1 mm.
FIG. 40 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 40. — Venezillo garimpeiro Campos-Filho, Borja-Arrieta & Bichuette, n. sp., male holotype, LES 28008: A, pereopod 1; B, pereopod 7; C, genital papilla; D, pleopod 1 exopod; E, pleopod 2 exopod; F, pleopod 3 exopod; G, pleopod 4 exopod; H, pleopod 5 exopod.
FIG. 49 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 49. — Distribution map of Porcellionides pruinosus (Brandt, 1833). Abbreviations of states: BA, Bahia; MG, Minas Gerais.
FIG. 24 in Shedding light into Brazilian subterranean isopods (Isopoda, Oniscidea): expanding distribution data and describing new taxa
FIG. 24. — Diploexochus carrapicho Campos-Filho, López-Orozco & Taiti, n. sp., female paratype LES 28001: A, dorsal habitus; B, lateral habitus; C, scale-seta; D, pereonite 1-7 epimera, ventral view; E, cephalon and pereonites 1-3, frontal view; F, cephalon and pereonite 1, back view; G, cephalon, dorsal view; H, pereonite 7, pleon, telson, and uropods, dorsal view; I, pleonites 4 and 5, telson and uropods, ventral view. Scale bar: A, 1 mm.
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.