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Figure 5 in Colotis lais (Butler, 1876) and Colotis euippe omphale (Godart, [1819]) use Cadaba aphylla (Thunb.) Wild LC as a host-plant at Tswalu Kalahari, Northern Cape Province, South Africa)
Figure 5 – Colotis euippe omphale male puddling (imbibing water and nutrients from wet soil) at a damp area near the Dedeben Research Centre, Tswalu Kalahari, South Africa, 22 December 2021. Photo: R.F. Terblanche.
Figure 3 in Colotis lais (Butler, 1876) and Colotis euippe omphale (Godart, [1819]) use Cadaba aphylla (Thunb.) Wild LC as a host-plant at Tswalu Kalahari, Northern Cape Province, South Africa)
Figure 3 – Colotis lais female resting on bare ground with open wings in typical fashion, north-west of the Dedeben Research Centre, Tswalu Kalahari, South Africa, 22 December 2021. Photo: R.F. Terblanche.
Figure 4 – Freshly emerged Colotis euippe omphale reared from a in Colotis lais (Butler, 1876) and Colotis euippe omphale (Godart, [1819]) use Cadaba aphylla (Thunb.) Wild LC as a host-plant at Tswalu Kalahari, Northern Cape Province, South Africa)
Figure 4 – Freshly emerged Colotis euippe omphale reared from a larva collected on 19 December 2021 on a Cadaba aphylla shrub, north of the Dedeben Research Centre, Tswalu Kalahari, South Africa. The CRG reference number for this rearing is RFT21H79. Photo: R.F. Terblanche.
Figure 2 in Colotis lais (Butler, 1876) and Colotis euippe omphale (Godart, [1819]) use Cadaba aphylla (Thunb.) Wild LC as a host-plant at Tswalu Kalahari, Northern Cape Province, South Africa)
Figure 2 – Colotis lais male, puddling (imbibing water and nutrients from wet soil) at a damp area near the Dedeben Research Centre, Tswalu Kalahari, South Africa, 24 December 2021. Photo: R.F. Terblanche.
Figure 1 in Colotis lais (Butler, 1876) and Colotis euippe omphale (Godart, [1819]) use Cadaba aphylla (Thunb.) Wild LC as a host-plant at Tswalu Kalahari, Northern Cape Province, South Africa)
Figure 1 – Freshly emerged adult male of Colotis lais reared from a larva collected on 19 December 2021 on a Cadaba aphylla shrub, north of the Dedeben Research Centre, Tswalu Kalahari, South Africa. The CRG reference number for this rearing is RFT21H78. Photo: R.F. Terblanche.
Haemobacteria in Colombian wild birds
<p>This is a database of genetic sequences obtained from a study aimed at identifying bacterial agents in the blood of a wild bird population captured in the municipality of Jardín (Antioquia, Colombia) through 16S qPCR and sequencing. A descriptive cross-sectional study was conducted using non-probabilistic convenience sampling. Blood samples were collected from wild birds captured using mist nets. Blood was drawn from each animal via puncture of the brachial vein using sterile lancets, with a drop of blood collected on filter paper for qPCR analysis. The 16S gene in bacterial genomes was detected in 13 out of 46 wild birds of the Passeriformes and quasi-Passeriformes orders, captured at three different locations within the study municipality at altitudes ranging from 1,665 to 2,034 meters above sea level. Seven different bird species were recorded, including five adults and one juvenile (when possible, to determine age group), as well as one male and one female (when possible, to determine sex), and four different haemobacteria were identified (i.e., <em>Exiguobacterium</em> spp., <em>Escherichia coli</em>, <em>Stenotrophomonas</em> spp., and <em>Stenotrophomonas maltophilia</em>).</p>
Expansion of the early warning system for avian influenza in the EU to evaluate the risk of spillover from wild birds to poultry
<p>GIF 1: Animated map of the spatiotemporal variations of the estimated number of infectious wild birds between February 2023 and March 2024</p> <p>GIF 2: Animated map of the spatiotemporal variations of transmission rate from wild birds to indoor chicken between February 2023 and March 2024</p> <p>GIF 3: Animated map of the spatiotemporal variations of transmission rate from wild birds to outdoor chicken between February 2023 and March 2024</p> <p>GIF 4: Animated map of the spatiotemporal variations of transmission rate from wild birds to indoor duck between February 2023 and March 2024</p> <p>GIF 5: Animated map of the spatiotemporal variations of transmission rate from wild birds to outdoor duck between February 2023 and March 2024</p> <p>GIF 6: Animated map of the spatiotemporal variations of the probability of HPAI introduction into indoor chicken farms between February 2023 and March 2024</p> <p>GIF 7: Animated map of the spatiotemporal variations of the probability of HPAI introduction into outdoor chicken farms between February 2023 and March 2024</p> <p>GIF 8: Animated map of the spatiotemporal variations of the probability of HPAI introduction into indoor duck farms between February 2023 and March 2024</p> <p>GIF 9: Animated map of the spatiotemporal variations of the probability of HPAI introduction into outdoor duck farms between February 2023 and March 2024</p> <p>GIF 10: Animated map of the spatiotemporal variations of the probability of HPAI introduction into poultry farms between February 2023 and March 2024 (scenario A)</p> <p>GIF 11: Animated map of the spatiotemporal variations of the probability of HPAI introduction into poultry farms between February 2023 and March 2024 (scenario B)</p>
Vitamin D status is heritable and under environment-dependent selection in the wild
<p>Vitamin D has a well-established role in skeletal health and is increasingly linked to chronic disease and mortality in humans and companion animals. Despite the clear significance of vitamin D for health and obvious implications for fitness under natural conditions, no longitudinal study has tested whether the circulating concentration of vitamin D is under natural selection in the wild. Here, we show that concentrations of dietary-derived vitamin D and endogenously-produced vitamin D metabolites are heritable and largely polygenic in a wild population of Soay sheep (<em>Ovis aries</em>). Vitamin D status was positively associated with female adult survival, and vitamin D status predicted female fecundity in particular, good environment years when sheep density and competition for resources was low. Our study provides evidence that vitamin D status has the potential to respond to selection, as well as new insights into how vitamin D metabolism is associated with fitness in the wild. </p>
Mutation Testing in the Wild: Findings from GitHub
<p>Supplementary material for the articule "Mutation Testing in the Wild: Findings from GitHub" submitted to the Empirical Software Engineering Journal. It includes:</p> <ul> <li>Literature_search_for_mutation_tools_2018-2021.xlsx. This document contains the papers found in the search for mutation testing tools performed between 2018 and 2021.</li> <li>Mutation_tools.xlsx: This document includes the 127 mutation testing tools identified in our study along with tables and graphs.</li> <li>Repositories_raw_data.xlsx: All repositories data mined from Github as evidence of use of the top 10 mutation tools analyzed in our study. In addition, tables with calculations and graphs used in our work are included.</li> <li>Search_strings_mutation_tools.xlsx: The search strings used to look for repositories using each mutation tool in Github.</li> </ul>
Fig. 2 in On the proper type designation for Camelina microcarpa, a wild relative and possible progenitor of the crop species C. sativa (Brassicaceae)
Fig. 2. – Isotype of Camelina microcarpa Andrz. ex DC. [KW, Besser herbarium: KW001003104; © National Herbarium of Ukraine, Kiev]
Fig. 1 in On the proper type designation for Camelina microcarpa, a wild relative and possible progenitor of the crop species C. sativa (Brassicaceae)
Fig. 1. – Isotype of Camelina microcarpa Andrz. ex DC. [KW, Besser herbarium: KW001003103; © National Herbarium of Ukraine, Kiev]
Fig. 1 in First record of a presumed wild common genet (Genetta genetta) in Switzerland
Fig. 1. Screen capture of the video recording a common genet (Genetta genetta) walking away from a camera trap set in the Châtillon forest, near Bernex, Geneva. This video was trigged by the genet on the 15th June 2019 at 09:58 p.m and is the second time that supposedly the same animal triggered the same camera six days earlier. The video recordings are available at https://doi.org/10.5281/zenodo.3617966.
Fig. 2 in Feeding and social behavior of the piabanha, Brycon devillei (Castelnau, 1855) (Characidae: Bryconinae) in the wild, with a note on following behavior
Fig. 2. Mean values of proportion of time expressing different foraging tactics by Brycon devillei for each season in the RPSP, between July 2006 and April 2009.
Fig. 3 in Feeding and social behavior of the piabanha, Brycon devillei (Castelnau, 1855) (Characidae: Bryconinae) in the wild, with a note on following behavior
Fig. 3. Two individuals of Brycon devillei aligned sideways to the timburé, Leporinus garmani, on a sand bank in the rio Preto channel. Photo by P. G. Azevedo.
Fig. 1 in Study of some European wild hybrids of Erica L. (Ericaceae), with descriptions of a new nothospecies: Erica nelsonii Fagúndez and a new nothosubspecies: Erica veitchii nothosubsp. asturica Fagúndez
Fig. 1. – Erica ×nelsonii Fagúndez. A. Synflorescence of upper left fragment (typus); B. General view of upper right fragment. [P. F. Hunt 1636, K] [Drawn by the author]
Fig. 2 in Study of some European wild hybrids of Erica L. (Ericaceae), with descriptions of a new nothospecies: Erica nelsonii Fagúndez and a new nothosubspecies: Erica veitchii nothosubsp. asturica Fagúndez
Fig. 2. – Seeds of different species of Erica L. A: Erica tetralix L.; B: E. tetralix (detail of surface cells); C: E. tetralix × E. ciliaris; D: E. tetralix × E. ciliaris (detail of surface cells); E: E. ciliaris L.; F: E. ciliaris (detail of surface cells). [A: Fagúndez s.n., SANT-BG [119]; B: Fagúndez s.n., SANT-BG [211]; C-D: Fagúndez 3266, SANT; E: Fagúndez & Reyes s.n., SANT-BG [266]; F: Fagúndez & Reyes s.n., SANT-BG [273]]
Genetic diversity of wild and cultivated Coffea canephora in northeastern DR Congo and the implications for conservation - Additional Data
<p>List of wild and cultivated <em>Coffea canephora </em>accessions from northeastern Democratic Republic of the Congo included in Vanden Abeele et al. 2021 - American Journal of Botany, and the corresponding alleles for each of the 18 microsatellite markers (0 indicates missing alleles).</p>
Figure 3 in Wild Relatives of the Eggplant (Solanum melongena L.: Solanaceae): New Understanding of Species Names in a Complex Group
Figure 3. Fruit shape and colour variation in cultivars of the common eggplant, Solanum melongena. Photograph taken by J. Prohens. doi:10.1371/journal.pone.0057039.g003
Figure 2. A in Wild Relatives of the Eggplant (Solanum melongena L.: Solanaceae): New Understanding of Species Names in a Complex Group
Figure 2. A sample of form and leaf variation in Solanum campylacanthum A.Rich. from across its morphological and geographical range showing the cline in leaf shape from south to north. A. Habit with narrow elliptic leaves. B. Habit with small leaves, small flowers, and dense curved prickles. C. Habit with ovate leaves and no prickles. D. Habit with large prickles and multiple fruits per infructescence. E. Habit with lobed leaves. F. Habit with cordate leaves. G. Short-stalked trichome from abaxial side of leaf. (Based on: A, Mott 11B, country; B, Gilfillan 6056, country; C, Torre 7145, Mozambique; D, Stewart E33, country; E, G, Friis et al. 8107, Ethiopia; F, Friis 8505, Ethiopia) Scale bar: A–F = 4 cm; G = 0.4 mm. Drawn by Lucy T. Smith. doi:10.1371/journal.pone.0057039.g002
Figure 1 in Wild Relatives of the Eggplant (Solanum melongena L.: Solanaceae): New Understanding of Species Names in a Complex Group
Figure 1. Representative flower and fruit morphology of eggplant and its wild relatives. A. Solanum campylacanthum inflorescences (Kenya - Vorontsova et al. 157); B. Solanum incanum immature fruit (Kenya – Vorontsova et al. 203); C. Solanum insanum fruit cross-section (China – Wang et al. 2047); D. Solanum insanum inflorescence with several hermaphrodite flowers (China – Wang et al. 2039); E. Solanum linnaeanum with yellow mature and mottled green immature fruit, note highly dissected leaves (Spain - Knapp IM-10096); F. Solanum melongena flower with duplicated parts (China – Wang et al. 2042). Photographs: A, B taken M.S. Vorontsova; C, D, E, F taken by S. Knapp. doi:10.1371/journal.pone.0057039.g001
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.