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Figure 4 Cunaxa minidiscondyla n in Additional contributions to the knowledge of Philippine predatory mites mainly of the subfamilies Cunaxinae and Cunaxoidinae (Acari: Prostigmata: Cunaxidae)
Figure 4 Cunaxa minidiscondyla n. sp., tritonymph: a – venter of idiosoma; b – leg I (trochanter to base of tarsus); c – leg II; d – leg III; e – leg IV. Scale bar 100 µm.
Figure 3 Cunaxa minidiscondyla n in Additional contributions to the knowledge of Philippine predatory mites mainly of the subfamilies Cunaxinae and Cunaxoidinae (Acari: Prostigmata: Cunaxidae)
Figure 3 Cunaxa minidiscondyla n. sp., female: a – Leg I; b – Leg II; c – Leg III; d – Leg IV. Scale bar 100 µm.
Data from: Resource addition drives taxonomic divergence and phylogenetic convergence of plant communities
1. Anthropogenic environmental changes are known to affect the Earth's ecosystems. However, how these changes influence assembly trajectories of the impacted communities remains a largely open question. 2. In this study, we investigated the effect of elevated nitrogen (N) deposition and increased precipitation on plant taxonomic and phylogenetic β-diversity in a 9-year field experiment in the temperate semi-arid steppe of Inner Mongolia, China. 3. We found that both N and water addition significantly increased taxonomic β-diversity, whereas N, not water, addition significantly increased phylogenetic β-diversity. After the differences in local species diversity were controlled using null models, the standard effect size of taxonomic β-diversity still increased with both N and water addition, while water, not N, addition, significantly reduced the standard effect size of phylogenetic β-diversity. The increased phylogenetic convergence observed in the water addition treatment was associated with the colonization of different, but phylogenetically closely related, species into different replicate plots of the treatment. Species colonization in this treatment was found to be trait-based, with leaf nitrogen concentration being the key functional trait. 4. Synthesis. Our analyses demonstrate that anthropogenic environmental changes may affect the assembly trajectories of plant communities at both taxonomic and phylogenetic scales. Our results also suggest that while stochastic processes may cause communities to diverge in species composition, deterministic process could still drive communities to converge in phylogenetic community structure.
Additional Data of O.Buß and S.Jager: "Statistical Evaluation of HTS Assays for Enzymatic Hydrolysis of ß-Keto Esters")
<p>The additional data set includes:</p> <ul> <li>Pdb structure files, which were used for calculations/pictures.</li> <li>R-scripts for calculation of statistical measures like Z-factor, SSMD and others.</li> <li>Data of different activity assays, which were used for R-script calculations.</li> <li>a SDS-PAGE (gel with all used enzymes)</li> </ul> <p>View our publication under: http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0146104</p>
Domain-specific model selection for structural identification of the Rab5-Rab7 dynamics in endocytosis - Additional Files
<p>Additional files from the manuscript titled "Domain-specific model selection for structural identification of the Rab5-Rab7 dynamics in endocytosis" published in BMC Systems Biology:</p> <ul> <li>Data containing delimited time points and measurements used for fitting the different model structures</li> <li>Supplementary material containing additional figures and tables</li> <li>Archive containing the complete library, the incomplete model and the task used for modeling the Rab5-Rab7 switch</li> </ul> <p> </p>
Additional plots referenced in Ghyselen (2016)
<p>The plots here included provide information on the linguistic repertoire structure in Ypres (Belgium) and accompany the chapter of Ghyselen (2016) in <em>The Future of Dialects</em> (eds.: Marie-Hélène Côté, Remco Knooihuizen & John Nerbonne).</p>
FIGURE 2. Dichogaster caraibensis n in New species of Dichogaster Beddard, 1888 (Clitellata: Benhamiidae) with additional records of earthworms from Guadeloupe (French West Indies)
FIGURE 2. Dichogaster caraibensis n. sp. A. Dorsal view, live photo. B. Ventral view, clitellum region. C. Spermatheca.
FIGURE 1. Dichogaster spolstoni n in New species of Dichogaster Beddard, 1888 (Clitellata: Benhamiidae) with additional records of earthworms from Guadeloupe (French West Indies)
FIGURE 1. Dichogaster spolstoni n. sp. A. Dorsal view, recently fixed. B. Ventral view. C. Ventral view clitellum region. D. Spermatheca.
Figure 1. from Additional moults into 'elongatus' males in laboratory-reared Polydesmus angustus Latzel, 1884 (Diplopoda, Polydesmida, Polydesmidae) – implications for taxonomy - ZooKeys 156: 41-48 (20 December 2011) https://doi.org/10.3897/zookeys.156.2045
Figure 1. - Dorsal view of a Polydesmus angustus male of stadium IX after its death at the age of 19 months. The trunk consists of 19 podous rings – bearing 32 pairs of legs plus regressed gonopods (8th leg-pair) – and one apodous ring anterior to the telson.
- Wings yellowish with apex blackish and an additional subapical transverse blackish band on fore wing (a); epicnemial carina very short, hardly extending onto mesopleuron (b) ………E. maynei Benoit, 1952 in A review of the Afrotropical Rhyssinae (Hymenoptera: Ichneumonidae) with the descriptions of five new species
- Wings yellowish with apex blackish and an additional subapical transverse blackish band on fore wing (a); epicnemial carina very short, hardly extending onto mesopleuron (b) ………E. maynei Benoit, 1952
Additional information to Research Letter "Immunogenicity of Cephalosporin Components in Non-IgE Mediated Cephalosporin Allergy"
<p>The file contains the following information:</p><p><strong>Additional information</strong></p><p><strong>Description</strong></p><p><strong>Page</strong></p><p>Materials and Methods</p><p>Study materials, syntheses of degradation products and enzyme-linked immunospot assay used in the study</p><p>1-3</p><p>Table 1</p><p>In vitro reactivity to different components of ceftriaxone degradation products in patients with positive ELISpot to ceftriaxone or cephalosporine with similar R1 side chain to ceftriaxone (N=21), categorized by underlying diseases and drug allergic phenotypes</p><p>4</p><p>Table 2</p><p>Clinical characteristics of patients with a confirmed non-IgE mediated hypersensitivity reaction to ceftriaxone or cephalosporin with a similar R1 side chain to ceftriaxone</p><p>5-6</p><p>Table 3</p><p>Frequencies of IFN-γ releasing cells and proportions of positive IFN-γ ELISpot assay upon stimulation with the suspected culprit drugs and different cephalosporins in patients with a history of non-IgE mediated reaction to ceftriaxone or cephalosporins with a similar R1 side chain (N= 21)</p><p>7-9</p><p>Figure captions and Figure legends</p><p> </p><p>Figure captions and figure legends for figures 1, 2, 3A, 3B, and 4.</p><p> </p><p>10</p><p> </p><p>Figure 1</p><p> </p><p>Mass spectrum results of the synthesized octalysine-ceftriaxone conjugates</p><p> </p><p> Figure 2</p><p>Chemical structures of cephalosporin components in this study</p><p> </p><p>Fig 3</p><p>Representative figures of IFN-γ releasing cells after stimulating PBMCs with different cephalosporins and their components, as demonstrated by ELISpot assay in two patients with a history of ceftriaxone-induced DRESS. Figure 3A shows the results for a single cephalosporin reactor, and Figure 3B shows the results for a multiple cephalosporin reactor.</p><p> </p><p>Fig 4</p><p>The frequencies of IFN-γ releasing cells and proportions of positive IFN-γ ELISpot assay upon stimulation with the suspected culprit drugs, other cephalosporins, and different components in patients with a history of non-IgE mediated reaction to ceftriaxone or cephalosporins with a similar R1 side chain (N= 21)</p><p> </p><p> </p>
Figure 6 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 6. Trestoncideres santossilvai, sp. nov. a) Holotype male, dorsal habitus. b) Allotype female, lateral habitus. c) Holotype male, close-up of head. d) Holotype male, close-up of pronotum.
Figure 5 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 5. Touroultia obscurella (Bates, 1865), holotype male? a) Dorsal habitus with original labels. b) Lateral habitus. c) Close-up of head. d) Close-up of pronotum.
Figure 3 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 3. Priscatoides tatila Dillon and Dillon, 1945, holotype female. a) Dorsal habitus. b) Lateral habitus with original labels. c) Close-up of head. d) Close-up of pronotum.
Figure 1 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 1. Jamesia ramirezi, sp. nov. a) Holotype female, dorsal habitus. b) Allotype male, ventral habitus.
Figure 4 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 4. Two species of Touroultia, gen. nov. a) T. lordi, sp. nov., holotype male, dorsal habitus. b) T. swifti, sp. nov., holotype male, dorsal habitus. c) T. lordi, sp. nov., holotype male, close-up of head. d) T. swifti, sp. nov., holotype male, close-up of head.
Figure 9 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 9. Malthonea cuprascens (Waterhouse, 1880), holotype. a) Dorsal habitus. b) Lateral habitus with original labels. c) Close-up of head. d) Close-up of pronotum
Figure 7 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 7. Nine species of Clavidesmus Dillon and Dillon, dorsal habitus. a) C. chicae Giorgi, 1998, holotype male. b) C. columbianus Breuning, 1961, holotype female. c) C. funerarius (Lane, 1958), holotype female. d) C. heterocerus (Buquet, 1852), holotype male. e) C. indistinctus Dillon and Dillon, 1952, holotype female. f) C. lichenigerus (Lane, 1958), holotype female. g) C. metallicus (Thomson, 1868), holotype female. h) C. monnei Giorgi, 1998, holotype male. i) C. rubigineus Dillon and Dillon, 1949, holotype female.
Figure 8 in New Taxa and Combinations in Onciderini Thomson, 1860 (Coleoptera: Cerambycidae: Lamiinae) from Central and South America, with notes on additional taxa Eugenio H. Nearns
Figure 8. Two species of Jamesia Jekel, 1861. a) J. lineata Fisher, 1926, holotype female, dorsal habitus with original labels. b) J. globifera Jekel, 1861, female, dorsal habitus. c) J. lineata Fisher, 1926, holotype, close-up of head. d) J. globifera Jekel, 1861, female, close-up of head.
Fig. 1 in Aphelocheirus (s.str.) freitagi nov.sp. from Mindoro Island and additional notes on Philippine Aphelocheiridae (Heteroptera)
Fig. 1: Aphelocheirus (s.str.) freitagi nov.sp., brachypterous male (paratype; body length 9.0 mm), dorsal aspect. Photo: © NHMW Hemiptera Image Collection, printed with permission.
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.