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Fig. 6 in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis
Fig. 6. Bayesian Inference tree (A) based on partial (478 bp) cytb sequences of Haemoproteus angustus n. sp. (lineage hCWT7) and the 20 closest related Haemoproteus lineages. Bayesian posterior probabilities and Maximum Likelihood bootstrap values were indicated above and below nodes, respectively. For each lineage, representative GenBank accession numbers and MalAvi lineage codes (if available) are indicated as well as the most common bird host. The scale bar indicates the expected mean number of substitutions per site according to the model of sequence evolution applied. Images B and C show the Median-Joining DNA haplotype network of partial (478 bp) cytb sequences of H. angustus hCWT7 and the 20 closest related Haemoproteus lineages. The upper image (B) shows the host distribution, and the lower image (C) depicts the geographic distribution according to the United Nations geoscheme. Each circle represents a unique haplotype/lineage. The frequency of each lineage is indicated for all haplotypes with more than one record and roughly corresponds to the size of circles. Bars on branches indicate the number of substitutions between two haplotypes. Small white circles represent median vectors, which are hypothetical (often ancestral or unsampled) sequences required to connect existing haplotypes with maximum parsimony.
Fig. 3 in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis
Fig. 3. Comparison of fully grown gametocytes of Haemoproteus angustus n. sp. (lineage hCWT7) from the blood of Curruca communis (A–D), H. belopolskyi (lineage hHIICT1) from the blood of Hippolais icterina (E–H) as well as H. parabelopolskyi (hSYAT2) (I–L), H. pallidulus (hSYAT3) (M–P), H. homogeneae (hSYAT16) (Q–T) and H. majoris (hWW2) (U–X) from the blood of Sylvia atricapilla. Note: the markedly attenuated gametocytes of the new species (A–D), which are not present in other Haemoproteus parasites (E–X); the fully grown gametocytes of H. belopolskyi (F, H) and H. parabelopolskyi (J, L) are bigger than those of H. angustus n. sp.; the pigment granules are predominantly roundish and small in H. pallidulus (M–P); the fully grown gametocytes are small and do not reach poles of infected erythrocytes in H. homogeneae (R, T); the erythrocyte nuclei are displaced laterally by H. majoris (V, X) – all these feature are not characteristic of H. angustus sp. nov. Symbols are the same as in Fig. 2. Giemsa-stained thin blood films. Scale bar = 10 µm.
Fig. 1. Bayesian phylogenetic tree constructed using partial cytochrome b in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis
Fig. 1. Bayesian phylogenetic tree constructed using partial cytochrome b sequences of 61 lineages of Haemoproteus, 4 lineages of Plasmodium, and Leucocytozoon sp. lSISKIN2 as outgroup. Posterior probabilities higher than 0.8 are indicated close to the respective nodes. Red font indicates the parasite lineage described in this publication. Vertical bars (A–D) show groups of closely related lineages, which complete development and produce gametocytes only in non-passerines (A, D), both non-passerines and passerines (B), and only passerines (C). Blue font indicates Haemoproteus species, which develop in non-passerine avian hosts, which are indicated by symbols (● – Psittaciformes; ∎ - Coraciiformes; ▴ - Strigiformes; ◆ - Anseriformes; ★ - Charadriiformes; ♥ - Pelecaniformes; ⋄ - Piciformes; ⊠ - Sphenisciformes; Ω - Musophagiformes; § - Trochiliformes; Ψ – Falconiformes; Σ – Columbiformes; Φ - Galliformes). Lineage names were provided (according to MalAvi database), followed by parasite species names and sequence GenBank accession numbers.
Fig. 5. Haemoproteus angustus n in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis
Fig. 5. Haemoproteus angustus n. sp. (lineage hCWT7) gametogenesis (A–H) and ookinete development (I–L) in vitro: A, B – initial stages of rounding up of gametocytes after the exposure of infected blood to air; C, E – rounded up macrogametocyte (C) and microgametocyte (E); F – the exflagellation; G – microgamete; H – fertilization; I – initial stage of ookinete development; J – medium differentiated ookinete; K – nearly mature ookinete with a residual body; L – mature ookinete without residual body. Note: the presence of several small residual bodies in erythrocytes containing gametocytes, which were preparing to escape from infected erythrocytes (A-C, E) – a unique character of this species during the initial stage of gametogenesis. Short triangle wide arrows – residual bodies; triangle arrowhead – macrogamete; triangle wide arrowheads – microgametes; short barbed arrows – finger-like outgrowth; long barbed arrows – apical end of developing ookinete; simple wide arrowhead – residual body of ookinete. Other symbols as in Fig. 2. Giemsa-stained thin blood films. Scale bar = 10 µm.
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 15. Drawing of autocorrelation function and partial correlation of the residues for males and females primary stage students
<p>After diagnosing and evaluating the models, the accommodating and the sufficiency of the models must be checked for males and females of primary stage students, through applying the compute (Ljung-Box Q) to check the model accommodation on the Function level 0.05 so the Q value occurs of males and females of primary stage students: Ljung-Box Q' = 1.10306, With p-value = P(Chi-square(1) > 1.10306) = 0.2936 Note that the Tabulated value equals 3.841 while the Q value is less than Tabulated value, so it takes the Null Hypothesis which manifests that the emptiness of the evaluated model out of the contrast in accordance trouble. It's possible to notice that the two parameters functions (Autocorrelation and Partial correlation Functions) of the residues for male females primary stage, in which the residues value is located within confidence interval limits, which means the residues series is random and the evaluated model is good and convenient as it is presented.</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 13. Drawing of autocorrelation Function and partial correlation of the residues for primary stage males students
<p>It's possible to notice the two parameters functions (Autocorrelation and Partial correlation Functions) of the residues for males primary stage, in which the residues value is located within the confidence interval limits which means the residues series is random and the Evaluated Model is good and convenient as it is presented.</p>
Stable Modeling on Resource Usage Parameters of MapReduce Application-Figure 2. ACF plot of Residuals of Regression Model of Terasort
<p>, are uncorrelated. If the error term is uncorrelated, it proves that there exists strong randomness in residuals of the model and provides the evidence for the unbiased estimate for the true standard error. The autocorrelation plot is used to check this assumption. Figure 2 shows the autocorrelation plot of residuals of regression models of TeraSort application. In Figure 2, the horizontal axis represents lag time and the vertical axis indicates the autocorrelation between residual at time t and residual at other lag time. At lag 0, autocorrelation is always equal to 1 and represents time series itself. Most of the autocorrelation at other lag time fall into the 95% confidence interval, only few of them violate the dashed line. Such a shape of ACF plot proves that residuals are uncorrelated and respects to the independent assumption of the linear regression model residuals.</p>
The Prediction of the Rate of the Dropout of the Primary Schools Students by Using the Genetic Algorithm-Figure 14. Drawing of autocorrelation function and partial correlation of the residues for primary stage males students
<p>After diagnosing and evaluating the models, the accommodating and the sufficiency of the models must be checked for primary stage female students, through applying the compute (Ljung- Box Q) to check the model accommodation on the function level 0.05 so the Q value occurs of primary stage female students: Ljung-Box Q' = 0.966626, With p-value = P(Chi-square(1) > 0.966626) = 0.3255 However, the Tabulated value equals 3.841 whilst the Q value is less than Tabulated value, so it accepts the Null Hypothesis which indicates the emptiness of the evaluated model out of the contrast accordance trouble. It's possible to notice the two parameters functions (Autocorrelation and Partial Correlation Functions) of the residues for females primary stage students, in which the residues value is located within the confidence interval limits, which means the residues series is random and the evaluated model is good and convenient as it is shown.</p>
Data providers package for reporting monitoring results for veterinary medicinal product residues (official data reporting phase)
<p>This data providers package provides the data collection configuration and supporting materials for reporting veterinary medicinal product residues (VMPR) results according to Council Directive 96/23/EC of 29 April 1996 on measures to monitor certain substances and residues thereof in live animals and animal products and repealing Directives 85/358/EEC and 86/469/EEC and Decisions 89/187/EEC and 91/664/EEC. These are to be used for the official data reporting phase.</p> <p>The package includes:</p> <p>Advice on the values to be reported for the mandatory fields specified for this data collection.</p> <p>The Standard Sample Description Version 2 XML schema definition for VMPR reporting.</p> <p>The STX transformation file which automatically assigns sampEventId and sampAnId when this information is not provided.</p> <p>The general and VMPR specific business rules applied for the automatic validation of the submitted datasets.</p> <p>The VMPR specific terminologies to be used for reporting analytical methods and the residues included in the scope of the analytical methods.</p> <p>An example of a reportable dataset following the Quick Start Reporting guide.</p> <p>Excel Mapping tool to convert excel files after mapping into XML document.</p> <p>Guidance on how to use the Excel Mapping tool.</p> <p>Guidance on how to run the validation report after submitting data to the DCF.</p>
SSD2 tool for Veterinary Medicinal Product Residues Occurrence Data
<p>Member States and other stakeholders can submit their Veterinary Medicinal Product Residues (VMPR) occurrence data using the EFSA mapping tool created for this purpose.</p> <p>Tools are structured in accordance with the SSD2 guidance and provide features that support manual data entry.Further details of reporting requirements can be found in the guidance ‘<a href="https://doi.org/10.5281/zenodo.2543210">Chemical Monitoring Reporting Guidelines (SSD2)</a>’</p> <p>Please read the instructions before using the tools.</p> <p><strong>This version replaces version 1 to fix a bug in the mapping tool.</strong></p>
Figure 2. A in Estimation of heavy metal residues from the feathers of Falconidae, Accipitridae, and Strigidae in Punjab, Pakistan
Figure 2. A comparison of concentrations (µg/g) of 6 different metals estimated from the feathers of raptors in 3 different regions of Punjab Province. Values expressed as mean ± SE.
Figure 1 in Organochlorine pesticide residues in feathers of four bird species from western part of Turkey
Figure 1. Specimen collecting locations from four geographical regions (A: Central Anatolia; B: Aegean; C: Mediterranean; D: Marmara; triangle: common buzzard, square; common kestrel; circle: common blackbird; ring: house sparrow) across Turkey.
Fig 2 in Relationship between field captures of Mediterranean fruit flies (Diptera: Tephritidae) and the residual amount and release rate of trimedlure from polymeric plugs
Fig 2. Captures of male medflies, Ceratitis capitata, in traps baited with fresh liquid trimedlure or weathered trimedlure plugs over the 12-wk study period in Florida in 2020 (top; means ± SE, N = 12 per treatment) and trimedlure content (means ± SD) and release rate from plugs over the study period (bottom, N = 5 per parameter).
Fig. 1 in Relationship between field captures of Mediterranean fruit flies (Diptera: Tephritidae) and the residual amount and release rate of trimedlure from polymeric plugs
Fig. 1. Captures of male medflies, Ceratitis capitata, in traps baited with fresh liquid trimedlure or weathered trimedlure plugs over the 10-wk study period in Hawaii in 2018 (top; means ± SE, N = 12 per treatment) and trimedlure content (means ± SD) and release rate from plugs over the study period (bottom, N = 5 per parameter).
Fig. 9 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids
Fig. 9. Species of the genus Pachycrommium Woodring, 1928, under UV light. A. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30476 (Faullummel coll.), Chaussy, Val d'Oise, France, Lutetian, in ventral view. B. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30874 (Faullummel coll.), Fontenay−en−Vexin, Eure, France, Lutetian, in ventral (B1) and dorsal (B2) views. C. Pachycrommium acuminatum, MNHN A25003 (Faullummel coll.), Chaussy, in dorsal view. D. Pachycrommium acuminatum (Lamarck, 1804), MNHN A25004 (Faullummel coll.), VilliersSaint−Frédéric, Yvelines, France, Lutetian, in apical view. E. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30479 (Faullummel coll.), Chaussy, in ventral view. F. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30875 (Faullummel coll.), Fontenay−en−Vexin, in ventral (F1) and dorsal (F2) views. G. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30872 (Faullummel coll.), Fontenay−en−Vexin, in ventral (G1) and dorsal (G2) views. H. Pachycrommium acuminatum (Lamarck, 1804), MNHN A30873 (Faullummel coll.), Fontenay−en−Vexin, in ventral (H1) and dorsal (H2) views. I. Pachycrommium eburnoides (Grateloup, 1847), MNHN A30405 (Faullummel coll.), Saint−Paul−lès−Dax, Landes, France, Burdigalian, in ventral (I1) and apical (I2) views. J. Pachycrommium eburnoides (Grateloup, 1847), MNHN A30411 (Cossman coll.), Dax, Landes, France, Early Miocene, in detailed view of the first whorls (J1) and apical (J2) view. K. Pachycrommium eburnoides (Grateloup, 1847), MNHN A30410 (Cossmann coll.), Dax, in ventral (K1), dorsal (K2), and apical (K3) views. Scale bars for all 10 mm, except 5 mm (I3, J2), 2 mm (J1). Photographs by C. Lemzaouda and P. Loubry (MNHN).
Fig. 8 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids
Fig. 8. Species of the genus Pachycrommium Woodring, 1928, under UV light. A. Pachycrommium suessoniensis (d'Orbigny, 1850), MNHN A30881 (Pacaud coll.), Celles−sur−Aisne, Aisne, France, Ypresian (Cuisian), in ventral (A1) and apical (A2) views. B. Pachycrommium suessoniensis (d'Orbigny, 1850), MNHN A30882 (Pacaud coll.), Celles−sur−Aisne, in apical (B1) and dorsal (B2) views. C. Pachycrommium productum (Deshayes, 1864), MNHN A30945 (Pacaud coll.), Chaussy, Val d'Oise, France, Lutetian, in dorsal view. D. Pachycrommium sp., MNHN A30482 (Pacaud coll.), Monampteuil, Aisne, France, Ypresian (Cuisian), in ventral (D1) and dorsal (D2) views. E. Pachycrommium scalariformis (Deshayes, 1825), MNHN A30401 (Ledon leg.), Fontenay−en−Vexin, Lutetian, in apical view. F. Pachycrommium scalariformis (Deshayes, 1825), MNHN A30402 (Ledon leg.), Fontenay−en−Vexin, view of a shell fragment. Scale bars 10 mm. Photographs by C. Lemzaouda and P. Loubry (MNHN).
Fig. 2 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids
Fig. 2. Species of the genus Ampullina Bowdich, 1822, under UV light. A. Ampullina depressa (Lamarck, 1804), MNHN J02192 (Cossmann coll.), Hérouval, Oise, France, Lutetian, in ventral (A1) and dorsal (A2) views. B. Ampullina parisiensis (d'Orbigny, 1850), MNHN A30403 (MNHN coll.), Villiers−Saint−Frédéric, Yvelines, France, Lutetian, in dorsal view. C. Ampullina parisiensis (d'Orbigny, 1850), MNHN B58545 (Lhomme coll.), Chavençon (La Tranchée), Oise, France, Priabonian, in abapertural (C1) and ventral (C2) views. D. Ampullina rustica (Deshayes, 1864), MNHN A30414 (Ledon coll.), Douains, Eure, France, Lutetian, in apical (D1) and dorsal (D2) views. E. Ampullina grossa (Deshayes, 1864), MNHN B58581 (MNHN coll.), Mont−Saint−Martin, Aisne, France, Bartonian (Auversian), in apical view. F. Ampullina chenayensis Cossmann, 1892, MNHN A31127 (Faullummel coll.), Chenay, Marne, France, Thanetian, in labral (F1) and dorsal (F2) views. G. Ampullina aizyensis (Bayan, 1870), MNHN A30408 (Ledon coll.), Bachivillers, Oise, France, Thanetian, in dorsal view. H. Ampullina aizyensis (Bayan, 1870), MNHN A30409 (Ledon coll.), Bachivillers, in ventral (H1) and abapertural (H2) views. I. Ampullina stampinensis (Cossmann and Lambert, 1884), syntype of Natica stampinensis MNHN J05147 (Lambert coll.), Saint−Hilaire (Pierrefitte), Essonne, France, Rupelian (Stampian), in dorsal view. J. Ampullina perusta (Defrance in Brongniart, 1823), MNHN A30821 (MNHN coll.), Ronca, Italy, Lutetian, in ventral (J1) and abapertural (J2) views. K. Ampullina perusta (Defrance in Brongniart, 1823), MNHN A30822 (MNHN coll.), Ronca, in dorsal view. Scale bars 10 mm. Photographs by C. Lemzaouda and P. Loubry (MNHN).
Fig. 5 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids
Fig. 5. Species of the genus Globularia Swainson, 1840, under UV light. A. Globularia (Globularia) peyreirensis (Cossmann and Peyrot, 1919), MNHN Cossmann (A30480 coll.), Peyreire, Gironde; France, Chattian, in dorsal (A1), abapertural (A2), labral (A3), and apical (A4) views. B.?Globularia (Globularia) pilula (Deshayes, 1864), MNHN J02181 (Cossmann coll.), Villiers−Saint−Frédéric, Yvelines, France, Lutetian, in ventral (B1) and dorsal (B2) views. C.?Globularia (Globularia) pilula (Deshayes, 1864), MNHN A30398 (MNHN coll.), Grignon, Yvelines, France, Lutetian, in ventral (C1) and dorsal (C2) views. D. Globularia (Cernina) fluctuata (Sowerby, 1825), MNHN IM (Staadt coll.), Banggi Island, Kudat division of Sabah, Malaysia, Recent, in ventral (D1), dorsal (D2), and labral (D3) views. E. Globularia (Cernina) fluctuata (Sowerby, 1825), MNHN IM (MNHN coll.), Philippines, Recent, in ventral (E1) and dorsal (E2) views. F. Globularia (Cernina) compressa (Basterot, 1825), MNHN A30399 (MNHN coll.), Mérignac, Gironde, France, Aquitanian, in dorsal (F1) and apical (F2) views. G. Globularia (Cernina) compressa (Basterot, 1825), MNHN A30400 (MNHN coll.), Mérignac, in dorsal view. H. Globularia (Cernina) sp., MNHN A30459 (Varone coll.), Saint−Martin−d'Oney, Landes, France, Aquitanian, in dorsal view. I. Globularia (Cernina) sp., MNHN A30460 (Varone coll.), Saint−Martin−d'Oney, in dorsal view. J. Globularia (Deshayesia) parisiensis (Raulin, 1844), MNHN A30892 (Cossmann coll.), Morigny (Château de Brunehaut), Essonne, France, Rupelian (Stampian), in labral (J1), abapertural (J2) and dorsal (J3) views. Scale bars 10 mm. Photographs by C. Lemzaouda and P. Loubry (MNHN).
Fig. 11 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids
Fig. 11. Comparisons of residual colour patterns between Naticidae and Ampullinidae under UV light. A–C. Naticidae. Indeterminate class: parallel zigzagging stripes, few zigzags per stripes, homogeneous zigzags' amplitude. A. Natica stoppanii Deshayes, 1864, MNHN A42002 (MNHN coll.), CuiseLamotte, Oise, France, Ypresian (Cuisian), in apical (A1) and dorsal (A2) views. B. Payraudeautia perforata (Deshayes, 1864), MNHN A31803 (MNHN coll.), Grignon, Yvelines, France, Lutetian, in dorsal view. C. Cepatia cepacea (Lamarck, 1804), MNHN B58269 (MNHN coll.), Croix−Blanche, France, Lutetian, in ventral view. D–F. Ampullinidae. Class II: non−parallel zigzagging stripes, numerous zigzags per stripes, heterogeneous zigzags' amplitude. D. Globularia (Cernina) compressa (Basterot, 1825), MNHN A30400 (MNHN coll.), Mérignac, Gironde, France, Aquitanian, in dorsal view. E. Globularia (s.s.) sigaretina (Lamarck, 1804), MNHN A30859 (MNHN coll.), Grignon, Yvelines, France, Lutetian, in dorsal view. F. Globularia (s.s.) semipatula (Deshayes, 1864), MNHN A30488 (Faullummel coll.), Cuise−Lamotte, Oise, France, Ypresian (Cuisian), in ventral view. Scale bars 10 mm for all, except 5 mm (B, C). Photographs by C. Lemzaouda and P. Loubry (MNHN).
Fig. 1 in Taxonomic implications of the residual colour patterns of ampullinid gastropods and their contribution to the discrimination from naticids
Fig. 1. Descriptive terminology of the residual colour patterns of the Ampullinidae. A. Crommium acutum (d'Orbigny, 1850), MNHN B58618 (MNHN coll.), Parnes, Oise, France, Lutetian, in ventral view. B. Globularia (Cernina) fluctuata (Sowerby, 1825), MNHN IM (Staadt coll.), Banggi Island, Kudat division of Sabah, Malaysia, Recent, in dorsal view. C. Ampullina parisiensis (d'Orbigny, 1850), MNHN A30403 (MNHN coll.), VilliersSaint−Frédéric, Yvelines, France, Lutetian, in dorsal view. D. Globularia (Deshayesia) parisiensis (Raulin, 1844), MNHN A30892 (Cossmann coll.), Morigny (Château de Brunehaut), Essonne, France, Rupelian (Stampian), in dorsal view. E. Ampullina rustica (Deshayes, 1864), MNHN A30414 (Ledon coll.), Douains, Eure, France, Lutetian, in apical view. F. Ampullina intermedia (Deshayes, 1832), MNHN A30416 (MNHN coll.), Cuise−la−Motte, Oise, France, Ypresian (Cuisian), in dorsal view. G. Ampullina intermedia (Deshayes, 1832), MNHN A30417 (MNHN coll.), Cuise−Lamotte, in labral view. Scale bars 10 mm. Photographs by C. Lemzaouda and P. Loubry (MNHN).
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.