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MERICS China Podcast: Austria, Denmark, Ireland, and their relations with China, with Alexander Davey, Lucas Erlbacher and Andreas Forsby

<p>European countries have become more aligned on how to deal with China in the past years, but national approaches towards the country still vary. In this episode of the MERICS China Podcast, we zoom in on Austria, Denmark, and Ireland and how their relationships with China have evolved, how they work with Brussels on China issues, and what is in store for the near future.<br><br><strong>Johannes Heller-John&nbsp;</strong>is joined by&nbsp;<strong>Alexander Davey</strong>, analyst at MERICS,&nbsp;<a href="https://www.aies.at/english/staff/erlbacher.php" target="_blank" rel="noopener noreferrer"><strong>Lucas Erlbacher</strong></a>, research associate with the Austrian Institute for European and Security Studies, and&nbsp;<a href="https://www.diis.dk/en/experts/andreas-boje-forsby" target="_blank" rel="noopener noreferrer"><strong>Andreas Forsby</strong></a>, senior researcher with the Danish Institute for International Studies. They contributed the country chapters for Ireland, Austria, and Denmark, respectively, in&nbsp;<a title="From a China strategy to no strategy at all: Exploring the diversity of European approaches" href="https://merics.org/en/report/china-strategy-no-strategy-all-exploring-diversity-european-approaches" target="_blank" rel="noopener">the most recent report of the European Thinktank Network on China (ETNC)</a>.</p>

opencc-by-4.0Dec 2023View details →
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Fig. 1 in Botanophila biclavata, a new species of Anthomyiidae (Brachycera, Diptera) from Austria

Fig. 1: Botanophila biclavata nov.sp. (male). (1) terminalia in lateral view, (2) cercal plate and surstyli in rear view, (3) sternite V.

opencc-by-4.0Dec 2023View details →
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Figs 2-5 in Botanophila biclavata, a new species of Anthomyiidae (Brachycera, Diptera) from Austria

Figs 2-5: (2-3) Botanophila biclavata nov.sp. (male); (4) Botanophila biclavata nov. sp., inner male genitalia; (5) Botanophila biclavata, nov.sp. (male), epandrium, cercal plate and surstyli, rear view.

opencc-by-4.0Dec 2023View details →
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Figs 4-8 in Description of a new species of Idiolispa FÖRSTER (Hymenoptera, Ichneumonidae, Cryptinae) from Austria

Figs 4-8: Holotype (♀) of Idiolispa vivarii nov.sp.; head dorsally (4), mesoscutum (5), propodeum dorsally (6), second tergite of metasoma (7), ovipositor tip (8).

opencc-by-4.0Dec 2023View details →
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Figs 1-3 in Description of a new species of Idiolispa FÖRSTER (Hymenoptera, Ichneumonidae, Cryptinae) from Austria

Figs 1-3: Holotype (♀) of Idiolispa vivarii nov.sp.; habitus laterally (1), base of antenna dorsally (2), head in facial view (3).

opencc-by-4.0Dec 2023View details →
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Figure 9 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 9. Additional phylogenetic analyses executed in TNT 1.5 for cross-checking results obtained from the main analysis. A, 50% majority rule consensus tree (tree length =148 steps, CI =0.57, RI =0.84) detected by excluding dental characters (59 to 70 of Supplemental material, Appendix A) from the main analysis; B, 50% majority rule consensus tree (tree length = 212 steps, CI = 0.46, RI = 0.76) detected using the New Technology Search analysis; C, 50% majority rule consensus tree (tree length = 212 steps, CI = 0.46, RI =0.76) detected by branch-and-bound method, using the swapping algorithm tree bisection reconnection (TBR) via 1000 replications; D, 50% majority rule consensus tree (tree length = 212, CI = 0.46, RI = 0.76) detected by branch-and-bound method, using the swapping algorithm tree bisection reconnection (TBR) via 100 replications, saving 100 trees per replication.

opencc-by-4.0Oct 2018View details →
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Figure 3 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 3. Ostarriraja parva gen. et sp. nov. from the early Miocene of Upper Austria, holotype, NHMW 2005z0283/0097. A, closeup of the head and pectoral region of the holotype under UV light; B, restoration. Abbreviations: ac, antorbital cartilage; cb, 5th ceratobranchial; fpf, fronto-parietal fontanelle; hyo, hyomandibula; mc, Meckel's cartilage; mes, mesopterygium; met, metapterygium; nc, nasal capsule; pa, pectoral arch; pq, palatoquadrate; pro, propterygium; rad, radials; syn, synarcual. Scale bars: 5 mm.

opencc-by-4.0Oct 2018View details →
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Figure 4 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 4. Anatomical details of some of the living skate representatives used for comparisons. A–D, Amblyraja sp., UNIVIE EMRG-Chond-H1, cleared and stained specimen; E, Raja clavata Linnaeus, 1758, UNIVIE EMRG-H2, micro-CT scan of the tail; A, overall view of the specimen in ventral view; B, close-up of the head and pectoral region; C, close-up of the pelvic girdle and fins; D, detail of the propterygial radials near the head region; note their reduced catenated calcification; E, detail of the vertebral column on the tail of UNIVIE EMRG-H2 in ventral view, showing the prismatic calcification of the cartilage forming the haemal arches. Abbreviations: ac, antorbital cartilage; bas, basipterygium; cb, 5th ceratobranchial; cr, compound radial; ha, haemal arches; hyo, hyomandibula; mc, Meckel's cartilage; mes, mesopterygium; met, metapterygium; nc, nasal capsule; pq, palatoquadrate; pro, propterygium; prp, prepelvic process; pub, puboischiadic bar; ro, rostral cartilage; sca, scapulocoracoid; syn, synarcual; th, thorns. Scale bars: A–C = 20 mm; D = 10 mm; E = 5 mm.

opencc-by-4.0Oct 2018View details →
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Figure 12. Cyclobatis oligodactylus Egerton, 1844 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 12. Cyclobatis oligodactylus Egerton, 1844 from the Late Cretaceous (Cenomanian) of Hjoula, Lebanon. A, MNHN F.HDJ505a; B, detail of the pelvic girdle and fins, showing the compound radial articulating with several radials in parallel fashion (arrow); C, detail of the head, showing the articulation of nasal capsules with propterygia (arrow); D, MNHN F.HDJ505b, counterpart, detail of the of the pectoral girdle showing the suprascapulae (arrow). The arrowheads in C and D show the distance between pro-, meso- and metacondyles. Scale bars: 10 mm.

opencc-by-4.0Oct 2018View details →
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Figure 8. The 50 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 8. The 50% majority rule consensus tree detected from the analysis of 74 morphological characters coded for 36 taxa showing the hypothetical relationships of Ostarriraja parva gen. et sp. nov. within Rajiformes. The list of synapomorphies on each node (capital letters) is given in Supplemental material, Table S1. Numbers below the nodes indicate the Bremer support.

opencc-by-4.0Oct 2018View details →
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Figure 10 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 10. Palaeobiogeography of skates from the Late Cretaceous to Neogene: 1 – Egypt, 2 – India, 3 – Arkansas, 4 – Maryland, 5 – Texas, 6 – Sweden, 7 – Antarctica, 8 – Belgium, 9 – Germany, 10 – South Carolina, 11 – Oregon, 12 – France, 13 – England, 14 – Jordan, 15 – Switzerland, 16 – Niger, 17 – Czech Republic, 18 – Mexico, 19 – Ukraine, 20 – Portugal, 21 – Netherlands, 22 – Denmark, 23 – Austria, 24 – Poland, 25 – Malta, 26 – Japan, 27 – Costa Rica, 28 – California, 29 – Italy, 30 – Slovakia, 31 – Argentina. Data from Fischer-Ooster (1866), Lawley (1876), Leriche (1927), Radwanski (1965), Steininger (1966), Jonet (1968), Ray et al. (1968), Cappetta (1970, 2012), Welton (1972), Herman (1974), Langenwalter (1975), Ceuster (1976), Steurbaut &amp; Herman (1978), Glaser (1979), Schultz (1979, 2013), Sahni &amp; Mehrotra (1980), Ward (1984), Itoigawa et al. (1985), Werner (1989), Cappetta &amp; Nolf (1991), Prasad &amp; Cappetta (1993), Welton &amp; Farish (1993), Long (1994), Hovestadt &amp; Hovestadt-Euler (1995), Case &amp; Cappetta (1997), Antunes et al. (1999), Laurito (1999), Muller (1999), Purdy et al. (2001), Siverson &amp; Cappetta (2001), Ward &amp; Bonavia (2001), Muller &amp; Rozenberg (2003), Reinecke et al. (2005), Roth &amp; Hoedemakers (2005), Adnet (2006), Becker et al. (2006), Cappetta &amp; Cavallo (2006), Sabol &amp; Kovac (2006), Antunes &amp; Balbino (2007), Cahuzac et al. (2007), Adnet &amp; Cappetta (2008), Gonźalez-Barba (2008), Wijnker et al. (2008), Brisswalter (2009), Cicimuri &amp; Knight (2009), Schultz et al. (2010), Boessenecker (2011, 2013), Cione et al. (2012), Reinecke (2015), Pollerspock &amp; Straube (2017), Engelbrecht et al. (2018). Maps are adopted and modified from Scotese (2002).

opencc-by-4.0Oct 2018View details →
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Figure 2 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 2. Ostarriraja parva gen. et sp. nov. from the early Miocene of Upper Austria. A, NHMW 2005z0283/0097a, holotype under normal light; B, NHMW 2005z0283/0097a, holotype under UV light; C, NHMW 2005z0283/0097b, holotype, counterpart under normal light; D, NHMW 2005z0283/0097b, holotype, counterpart under UV light. Scale bars: 10 mm.

opencc-by-4.0Oct 2018View details →
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Figure 1. A in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 1. A, location and simplified geological map of Upper Austria, based on Rupp et al. (2008), showing the position of the locality (red dot) where Ostarriraja parva gen. et sp. nov. was found. B, palaeogeographical sketch-maps of the Paratethys seas during the Ottnangian, middle Burdigalian, early Miocene showing the possible location of the locality in A, based on Rogl (1998).

opencc-by-4.0Oct 2018View details →
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Figure 5 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 5. Ostarriraja parva gen. et sp. nov. from the early Miocene of Upper Austria, holotype, NHMW 2005z0283/0097. A, closeup of the tail with the anterior part on the left side; B, detail of the radials in the pectoral disc; C, close-up of the teeth; D, detail of some tail thorns. Abbreviations: mc, Meckel's cartilage; pq, palatoquadrate; th, thorns; vc, vertebral centra. The arrows indicate the rostral direction. Scale bars: A–C = 1 mm; D = 0.5 mm.

opencc-by-4.0Oct 2018View details →
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Figure 6 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 6. Ostarriraja parva gen. et sp. nov. from the early Miocene of Upper Austria. A, NHMW 2005z0283/0097, close-up of the pelvic girdle and fins of the holotype under UV light; B, restoration. Abbreviations: bas, basipterygium; cr, compound radial; prp, prepelvic process; pub, puboischiadic bar; rad, radials. Scale bars: 10 mm.

opencc-by-4.0Oct 2018View details →
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Figure 7 in A new Miocene skate from the Central Paratethys (Upper Austria): the first unambiguous skeletal record for the Rajiformes (Chondrichthyes: Batomorphii)

Figure 7. Ostarriraja parva gen. et sp. nov. from the early Miocene of Upper Austria. Three isolated teeth from the holotype NHMW 2005z0283/0097 in A, occlusal; B, lingual; C, labial; and D, lateral view. Scale bar: 200 µm.

opencc-by-4.0Oct 2018View details →
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Vulnerability tools - Austrian Alps (Austria)

<p>The MOVING project has developed accessible <strong>tools </strong>designed to assess susceptibility and vulnerability within the region, ready to be used by both experts and the general audience. This document synthesises crucial information for the Austrian Alps Region, particularly focusing on the Participatory Vulnerability Matrix and the Spatial Vulnerability Map. Furthermore, it includes <strong>supplementary maps and figures </strong>detailing various aspects such as the delineation of Reference Landscape, distribution of land systems, areas affected by wildfires, susceptibility to floods across different return periods, severity of forest disturbances, rainfall erosivity, and more.</p>

opencc-by-4.0Apr 2024View details →
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Common bunt in wheat: Results of the ECOBREED field trials, Austria and Czech Republic, 2021-2022

<p>Supplementary material to Lunzer et al. (2023) Front Plant Sci 14: 1264458 [https://doi.org/10.3389/fpls.2023.1264458]:</p> <ul> <li>Scheme for the marker-assisted selection for common bunt QTL</li> <li>Raw data of field and lab evaluations - Austria &amp; Czech Republic 2021</li> <li>Raw data of field and lab evaluaitons - Austria &amp; Czech Republic 2022</li> </ul> <p>Raw data files include the data on several spreadsheet sheets. Each file includes metadata and used abbreviations in the first two sheets.</p>

opencc-by-4.0Apr 2024View details →
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National Checklists: Austria Species List

Data from: GBIF.org (23 January 2025) GBIF Occurrence Download <a href="https://doi.org/10.15468/dl.vd2ajk" target="_blank" rel="noopener">https://doi.org/10.15468/dl.vd2ajk</a>

opencc-zeroAug 2024View details →
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Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Austria

<p>This dataset contains the monitoring results of veterinary medicinal product residues and other substances measured in live animals and animal products analysed by the national competent authority of Austria. The presence of unauthorised substances, residues of veterinary medicinal products in food may pose a risk factor for public health.</p> <p>For this reason and in order to ensure a high level of consumer protection, a comprehensive legislative framework has been established in the European Union (EU) which defines maximum limits permitted in food and monitoring programmes for the control of the presence of these substances in the food chain. Regulation (EU) No 37/2010 establishes maximum limits for residues of veterinary medicinal products in food-producing animals and animal products. Maximum residue levels for pesticides in or on food and feed of plant and animal origin are laid down in Regulation (EC) No 396/2005. &nbsp;Commission Implementing Regulation (EU) 2022/1646 lays down practical arrangements for and specific content of official controls of the use of veterinary medicinal products in live animals and products of animal origin through three different official national control plans: a national risk-based control plan for production in the Member States, a national randomised surveillance plan for production in the Member States and a national risk-based control plan for third-country imports. Additionally, Commission Delegated Regulation (EU) 2022/1644 lays down the range of samples and stage of production, processing and distribution at which the samples are to be taken.</p> <p>Since 2018 until 2022, the data on the national residue monitoring plan were reported to EFSA in accordance with Council Directive 96/23/EC.</p> <p>The dataset contains the results of laboratory tests from samples taken from bovines, pigs, sheep, goats, horses, poultry, rabbits, farmed game, wild game aquaculture, milk, eggs and honey, and from 2023 also samples from casings, insects and reptiles.</p> <p>Targeted samples are taken with the aim of detecting illegal treatment or controlling compliance with the maximum levels laid down in the relevant legislation. This means that, in their national plans Member States target the groups of animals (species, gender, age) where the probability of finding residues is the highest. Conversely, the objective of random sampling is to collect significant data to evaluate, for example, consumer exposure to a specific substance.</p> <p>Suspect samples are taken as a consequence of i) non-compliant results on samples taken in accordance with the control plans, ii) possession or presence of prohibited substances at any point during manufacture, storage, distribution or sale through the food and feed production chain, or iii) suspicion or evidence of illegal treatment or non-compliance with the withdrawal period for an authorised medicinal veterinary product.</p> <p>Residues of pharmacologically active substances mean active substances, excipients or degradation products and their metabolites, which remain in food.</p> <p>Unauthorised substances mean substances that are not authorised as veterinary medicinal products or as a feed additive under European Union legislation.</p> <p>Prohibited substances mean substances which are prohibited for use in food producing animals according to the European Union legislation.</p> <p>Non-compliant sample is a sample that has been analysed for the presence of one or more substances and failed to comply with the legal provisions for at least one substance. Thus, a sample can be non-compliant for one or more substances.</p> <p><strong>REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION:</strong></p> <p>VMPR_2023 &ndash; Austrian Agency for Health and Food Safety</p> <p>VMPR_2022 &ndash; Austrian Agency for Health and Food Safety</p> <p>VMPR_2021 &ndash; Austrian Agency for Health and Food Safety</p> <p>VMPR_2020&nbsp;&ndash;&nbsp;Austrian Agency for Health and Food Safety</p> <p>VMPR_2019 &ndash;&nbsp;Austrian Agency for Health and Food Safety</p> <p>VMPR_2018 &ndash;&nbsp;Austrian Agency for Health and Food Safety</p> <p>VMPR_2017&nbsp;&ndash;&nbsp;Austrian Agency for Health and Food Safety</p>

opencc-by-4.0May 2019View details →

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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.

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