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Animal disease data complementing the European Union One Health 2020 Zoonoses Report

This dataset contains the mandatory annual data reported for bovine tuberculosis and for bovine and ovine and caprine brucellosis based on Directive 2003/99 that cites in Recital 7 the Council Directives 64/432/EEC and 91/68/EEC. The relevant Commission Decisions relating to the officially free (OF) MS and MS' regions and related reporting are: Decision 2003/467/EC for bovine tuberculosis and bovine brucellosis, and Decision 93/52/EC for sheep and goat brucellosis (B. melitensis). REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: Disease_status_data_2020_20211109: >>

Prevalence data complementing the European Union One Health 2020 Zoonoses Report

This dataset contains monitoring data on zoonoses and zoonotic agents under the Directive 2003/99/EC. This Directive requires Member Sates (MSs) to collect, evaluate and report data on zoonoses and zoonotic agents. MSs can also report monitoring data and information on some other pathogenic microbiological agents in foodstuffs. Relevant EU legislation: Commission Regulation (EC) No 2073/2005,Commission Regulation (EC) No 1441/2007, Commission Regulation (EU) No 1086/2011, Commission Regulation (EU) No 209/2013, Commission Regulation(EU) No 217/2014. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: Prev_data_2020 >>

Sample based prevalence data complementing the European Union One Health 2020 Zoonoses Report - the United kingdom

Sample based prevalence data complementing the European Union One Health 2020 Zoonoses Report - Finland

Sample based prevalence data complementing the European Union One Health 2020 Zoonoses Report - Sweden

Supporting data for the AI education publication statistics in "An Experience Report of Executive-Level Artificial Intelligence Education in the United Arab Emirates"

Supporting data for the AI education publication statistics presented in the paper "An Experience Report of Executive-Level Artificial Intelligence Education in the United Arab Emirates" to be published at the Twelfth AAAI Symposium on Educational Advances in Artificial Intelligence (EAAI-22). The data was used to plot the figure showing the cumulative number of publications from 1976 to 2020 relating to AI education.

FIG. 6. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 6. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: left anterior part of the shell in oblique posterolateral view showing the delimitation of marginals 2 and 3, and of plastral scutes by the indentation at the end of sulci border, and the ventral bulges of the scutes. Abbreviations: ax b, axillary buttress; 3d per, third peripheral. The arrows indicate ends of sulci at the border of the peripherals and anterior plastral lobe. Scale bar: 5 cm.

FIG. 9 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 9. — Comparison of the decoration of Sindhochelys ragei n. gen., n. sp. from the Paleocene of Ranikot, locality K18-12, Southern Pakistan, and Taphrosphys sulcatus (Leidy, 1856) from the early Paleocene of New Jersey (United States): A-D, Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3: A, nuchal part; B, left peripherals 2, dorsal face with smaller polygons than in other parts; C, suprapygal-pygal part, dorsal views; D, imprint of an isolated plate, ventral view; E-G, Taphrosphys sulcatus: E, AMNH 1470, "Barnsboro, N.J." (Cope collections), nuchal border of three plates, dorsal view; F, G, AMNH 2522, «Tinton Falls, N.J.», syntype: F, peripheral 6 (medial plate of three in Leidy (1856: pl. 19, fig.4), and in Gaffney et al. (2006: fig. 20), dorsal view; G, xiphiplastron, ventral view. Scale bars: A-C, E-G, 5 cm; D, 2 cm.

FIG. 10 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 10. — Fragmentary part of a carapace of an undetermined Bothremydidae, from the Paleocene of Ranikot, locality K18-12, CPAG-RANKT-V4, Southern Pakistan: A, B, ventral and dorsal views; C, detail of the dorsal decoration. Abbreviations: cost3, costal 3; cost5, costal 5; pcs, suture of the peripheral border with the border of plastral processes; per 5-8, peripherals 5, 6, 7, 8; perf, pholad perforations. Scale bars: A, B, 4 cm; C, 1 cm.

FIG. 5. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 5. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: A, anterolateral part of the carapace after removal of a part of the costal 1 with part of the neural l and the costal 2, to show the imprints of the thoracic ribs 1 and 2, and axillary buttress, in dorsal view; B, same removed part in ventral view. Abbreviations: ax b, axillary buttress; cost 1, costal 1; n1, neural 1; nu, nuchal; per 2, peripheral 2; rib 1, rib 2, medial part of thoracic ribs 1 and 2. Scale bar: 4 cm.

FIG. 4. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 4. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: A, B, shell drawings, in dorsal (A) and ventral (B) views. Scale bars: 10 cm.

FIG. 1 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 1. — Location and stratigraphic position of fossil material: A, location of the Laki Range in eastern Sindh Province, southern Pakistan, and simplified geological map of the Ranikot Fort area (adapted from Schelling 1999); B, stratigraphic position of the fossil assemblage within the Waddi Sawri section. Note that the base of this section is close to the base of the Khadro Formation; in this area the thickness of the Khadro Formation is c. 80 m, and the fossil locality K18-12 is in the lower Khadro Formation.

FIG. 3. — Sindhochelys ragei n. gen., n in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 3. — Sindhochelys ragei n. gen., n. sp., holotype CPAG-RANKT-V-3, from the Paleocene of Ranikot, locality K18-12, Southern Pakistan: A, B, shell photographs in dorsal (A) and ventral (B) views. Scale bar: 10 cm.

FIG. 2 in First report of a bothremydid turtle, Sindhochelys ragei n. gen., n. sp., from the early Paleocene of Pakistan, systematic and palaeobiogeographic implications

FIG. 2. — Turtle shell, CPAG-RANKT-V-3, holotype of Sindhochelys ragei n. gen., n. sp., in situ, during and after excavation at the locality K18-12: A, carapace in posterior view; A1, close-up of a lateral border showing the presence of a venerid bivalve in life position inside the carapace; B, carapace in dorsal view after excavation and split into three blocks. Scale bar: 30 cm.

Figure 89 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report

Figure 89: Reconstruction of the maximum glacial extent during the high point of the last ice-age (26 – 20 thousand years ago). Figure adapted from the publication Geologische Bundesanstalt (Hrsg.) (2013): Der Alpenraum zum Höhepunkt der letzten Eiszeit – Posterkarte. Geologische Bundesanstalt, Wien.

Figure 90 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report

Figure 90: Representation of the seasonal cycle of stratification and mixing in a dimictic lake throughout a year.

Figure 88 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report

Figure 88: Water temperature in lakes of the Po river catchment (orange) were generally warmer than in lakes of the Rhone (green) and Rhine (red) catchments. The lakes on the northern edge of the Alps remain cooler in summer and the lakes in the south remain warmer in winter. Upper panel shows 95 % quartile and lower panel shows 5% quartile of monthly mean lake surface water temperatures based on remote sensing (Advanced Very High Resolution Radiometer; 1989 – 2014 [214]). Quar- tiles were used rather than true minimum/maximum to avoid the effects of outliers.

Figure 85 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report

Figure 85: Histograms showing variation in lake surface area (left column), lake maximum depth (middle column) and height above sea level (altitude; right column) among the major catchments.

Figure 84 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report

Figure 84: Distance among lakes by river in the Rhine (upper panel), Rhone (middle panel) and Po (lower panel) river catchments.

Figure 81 in Diversity, distribution and community composition of fish in perialpine lakes – "Projet Lac" synthesis report

Figure 81: Depth distribution of fish weight (biomass per unit effort) in pelagic habitats to 50 m deep according to deep-set vertical nets (fish in the 3 m of net close to the lake floor were excluded).