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FIGURE 3 in Late Oligocene decapod crustaceans from the Trbovlje Formation of Slovenia, with a description of two new species of hymenosomatid crabs
FIGURE 3. Halicarcinus popeius sp. nov., schematic reconstruction. A. Carapace in dorsal view; B. Detailed view of second type of rostrum and robust chelipeds (male); C. Third pereopod (P3) with detailed view of dactylus.
FIGURE 1 in Late Oligocene decapod crustaceans from the Trbovlje Formation of Slovenia, with a description of two new species of hymenosomatid crabs
FIGURE 1. Simplified geographical map of Slovenia showing (marked with star) the fossiliferous locality "Neža" near Trbovlje.
FIGURE 7 in Late Oligocene decapod crustaceans from the Trbovlje Formation of Slovenia, with a description of two new species of hymenosomatid crabs
FIGURE 7. Carapace length vs. maximum carapace width of hymenosomatid specimens from the "Neža" locality. Halicarcinus popeius sp. nov. are marked in blue triangles (circles when trapezoid rostrum), Lucascinus trifailensis sp. nov. specimens are marked with orange squares. All measurements in mm.
FIGURE 2 in Late Oligocene decapod crustaceans from the Trbovlje Formation of Slovenia, with a description of two new species of hymenosomatid crabs
FIGURE 2. Lithostratigraphic section showing exposed strata at the "Neža" locality. Depths on the right indicate the fish fauna mass mortality layers (marked with a fish icon) and layers with fossil hymenosomatid crabs, which are marked with a crab icon.
National Checklists: Slovenia 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>
Results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products - Slovenia
<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 Slovenia. 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. 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 – Ministry of Agriculture, Forestry and Food</p> <p>VMPR_2022 – Ministry of Agriculture, Forestry and Food</p> <p>VMPR_2021 – Ministry of Agriculture, Forestry and Food</p> <p>VMPR_2020 – Ministry of Agriculture, Forestry and Food</p> <p>VMPR_2019 – Ministry of Agriculture, Forestry and Food</p> <p>VMPR_2018 – Ministry of Agriculture, Forestry and Food</p> <p>VMPR_2017 – Ministry of Agriculture, Forestry and Food</p>
FIGURE 6. Non-xiphosurid euarthropods from the Strelovec Formation. A, E in Revisiting horseshoe crab fossils from the Middle Triassic (Anisian) Strelovec Formation Konservat-Lagerstätte of Slovenia
FIGURE 6. Non-xiphosurid euarthropods from the Strelovec Formation. A, E: Aeger sp. A: PMSL T-1270. E: PMSL T- 1238 showing exceptional appendage detail. B: An as-of-yet undescribed thylacocephalan. PMSL T-1742. C, D: Exceptionally well-preserved indeterminate decapod crustaceans. C: PMSL T-1262 showing appendage segmentation and ocular structures. D: PMSL T-1263. F: Schimperella sp. PMSL T-1236. Image credit: Jure Žalohar.
FIGURE 4 in Revisiting horseshoe crab fossils from the Middle Triassic (Anisian) Strelovec Formation Konservat-Lagerstätte of Slovenia
FIGURE 4. Additional xiphosurids with genal spine indentations. Arrows indicate the structure on all taxa. A: Franconiolimulus pochankei from the Bayreuth Formation, (Early Jurassic, Hettangian) Pechgraben, Germany. SSN 8PG35, holotype. B, C: Panduralimulus babcocki from the Maybelle Limestone, Lueders Formation (Permian, Cisuralian, Kungurian), Texas, USA. B: USNM 520723, holotype. C: USNM 520724, paratype. D: Tasmaniolimulus patersoni from the Jackey Shale (Permian, Lopingian), Tasmania, Australia. UTGD 123979, holotype. E: Dubbolimulus peetae from the Ballimore Formation (Middle Triassic, Ladinian), New South Wales, Australia. MMF 27693, holotype. D coated in ammonium chloride sublimate. D and E converted to greyscale. Image credit: A: Andreas Hecker; B–D: Russell Bicknell; E: David Barnes.
FIGURE 3 in Revisiting horseshoe crab fossils from the Middle Triassic (Anisian) Strelovec Formation Konservat-Lagerstätte of Slovenia
FIGURE 3. New material referred to Sloveniolimulus rudkini. A, B, E: PMSL T-2071. A: Specimen showing prosomal doublure and possible occipital lobe on left genal spine. B: Interpretative drawing of PMSL T-2071. E: Close up of phosphatized spheres in A. C, D: PMSL T-2072. C: Specimen showing injured right genal spine and hypertrophied left genal spine. D: Interpretative drawing of PMSL T-2072. Specimens from the Western slopes of the Kalška gora Mountain, within the Kamniška Bistrica Valley. B and D colour coded for main body sections. A and C coated in ammonium chloride sublimate. All images converted to greyscale. Abbreviations: Car: cardiac lobe; In: genal spine indentation; Oc: possible occipital lobe; Pro: prosoma; Thr: thoracetron. Image credit: A, C: Russell Bicknell; E: Tomaž Hitij.
FIGURE 2 in Revisiting horseshoe crab fossils from the Middle Triassic (Anisian) Strelovec Formation Konservat-Lagerstätte of Slovenia
FIGURE 2. Holotype of Sloveniolimulus rudkini. A: PMSL T-993. B: Interpretative drawing of PMSL T-993, colour coded for main body sections. Specimen from the Section S1 of the Slatinski Plaz, Robanov Kot Valley. A coated in ammonium chloride sublimate and images converted to greyscale. Abbreviations: Car: cardiac lobe; Fla: thoracetronic flange; In: genal spine indentation; Med: medial thoracetronic lobe; Oph: ophthalmic ridge; PDub: prosomal doublure; Pro: prosoma; TDub: thoracetronic doublure; Thr: thoracetron; Tel: telson; Tk: telson keel. Image credit: Russell Bicknell.
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig.15 Scanning electron micrographs (SEM) showing transverse rows of dentition on Dinaride Zospeum and Iberozospeum radulae; (a) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia, transverse rows of teeth on long, slender basal plates (bp), rachidian (r) and lateral teeth (l), arrows indicate medial grooves on mesocones of individual teeth; (b) Z. isselianum, NMBE 553389, Turjeva jama, Slovenia, ibid.; (c) Iberozospeum sp. (RMNH.MOL.234,116), Cueva a Sul, straight transverse rows of small, seemingly bi-cuspid lateral teeth (l) with reduced mesocones on compact basal plates; (d) ibid., close up view of rachidian teeth (r), lateral fang-like teeth (l) and transitional teeth (t); (e) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili, rachidian teeth (r) flanked by 4-cuspid lateral teeth (l), C. ibazoricum-like in form; (f) Iberozospeum sp. (RMNH. MOL.234108), Cueva la Torcona, lateral teeth showing reduced mesocones (me) flanked by long, fang-like endo- and ectocones (e), rachidian tooth (r) (flipped over in upper righthand corner of image); (g) I. zaldivarae (AJC 1876a), Cueva de Las Paúles, transverse rows of teeth showing varying cusp lengths; (h) ibid., close up view (left to right) of marginal (m) and transitional teeth (t) on short, compact basal plates (bp). — Magnification varies for each perspective, see scale bars; all Figs taken by M. Ruppel, (ret.) Goethe University Frankfurt am Main
◂Fig. 13 Crystallographic structure on the columellar lamellae of Dinaride Zospeum and Iberozospeum shells; (a) Zospeum spelaeum, (AJC 847), Betalov Spodmol jama, Slovenia (45.7922 14.1877), pattern of low, non-overlapping, wedges of crystallographic structure on the lamella; (b) Zospeum spelaeum, (MCBI CSR SASA 37049a), Velika Pasica, Slovenia (N45.9189 E14.4934), non-overlapping wedges of crystallographic structure on lamella in old shell; (c) Iberozospeum sp., (RMNH.MOL. 234,120), Cueva Refugio, Trucios, overview of dense, overlapping, scale-like wedges of localized, crystallographic structure on upper part of the lower lamella; (d) ibid., closeup view of c; (e) Iberozospeum sp., (RMNH.MOL. 234,104), Cueva del Comediante, Santander, upper part of the lamella of chemically treated shell showing dense, overlapping wedges of localized, crystallographic structure; (f) Iberozospeum sp., (RMNH. MOL. 234,141), Cueva a Sul, Oviedo, localized, overlapping wedges of crystallographic structure on lamella of chemically treated shell; (g) Iberozospeum vasconicum, (AJC 1849), Cueva Arrikrutz, overview of dense, localized, crystallographic structure on lower part of the lamella; h, ibid., closeup view of g. — Magnification varies for each perspective, see scale bars; Figs. a–b, g–h) imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main; Figs. c–f imaged by Dirk Vendermarel, Naturalis Biodiversity Center in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 13 Crystallographic structure on the columellar lamellae of Dinaride Zospeum and Iberozospeum shells; (a) Zospeum spelaeum, (AJC 847), Betalov Spodmol jama, Slovenia (45.7922 14.1877), pattern of low, non-overlapping, wedges of crystallographic structure on the lamella; (b) Zospeum spelaeum, (MCBI CSR SASA 37049a), Velika Pasica, Slovenia (N45.9189 E14.4934), non-overlapping wedges of crystallographic structure on lamella in old shell; (c) Iberozospeum sp., (RMNH.MOL. 234,120), Cueva Refugio, Trucios, overview of dense, overlapping, scale-like wedges of localized, crystallographic structure on upper part of the lower lamella; (d) ibid., closeup view of c; (e) Iberozospeum sp., (RMNH.MOL. 234,104), Cueva del Comediante, Santander, upper part of the lamella of chemically treated shell showing dense, overlapping wedges of localized, crystallographic structure; (f) Iberozospeum sp., (RMNH. MOL. 234,141), Cueva a Sul, Oviedo, localized, overlapping wedges of crystallographic structure on lamella of chemically treated shell; (g) Iberozospeum vasconicum, (AJC 1849), Cueva Arrikrutz, overview of dense, localized, crystallographic structure on lower part of the lamella; h, ibid., closeup view of g. — Magnification varies for each perspective, see scale bars; Figs. a–b, g–h) imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main; Figs. c–f imaged by Dirk Vendermarel, Naturalis Biodiversity Center
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main in Molecular investigation and description of Iberozospeum n. gen., including the description of one new species (Eupulmonata, Ellobioidea, Carychiidae)
◂Fig. 14 Scanning electron micrographs (SEM) showing radular ribbon form, middle adhesive zone (az) and rows of dentition (rd) of Dinaride and Iberian individuals (notation denotes aspects on one Dinaride Zospeum and one Iberozospeum ribbon); (a) Z. exiguum (NMBE 553384), Križna jama, Slovenia (45.7452, 14.4673), long and narrow, tapered anterior end (tae), short adhesive zone (az), bottom furled with narrow obtuse or straight base (nosb); (b) Z. pretneri, (NMBE 553290), Gornja Cerovačka pećina, Croatia (44.2701, 15.8855), ibid., with straight base; (c) I. vasconicum, (AJC 1848), Cueva Ermita de Sandaili (42.9994, -2.4381), moderately long and broad, tapered anterior end (tae), prominent adhesive zone (az), straight base (sb); (d) I. zaldivarae, (AJC 1876), Cueva de Las Paúles (43.1282, -2.7362), ibid.; (e) Iberozospeum sp. (RMNH.MOL. 234,109), Cueva de la Foz, long and broad, ibid; (f) Iberozospeum sp., (RMNH.MOL. 234,144), Cueva de Rales, very long and broad, ibid; (g) Iberozospeum sp., (RMNH.MOL. 234,116), Cueva a Sul, long and broad, ibid; (h) Iberozospeum sp., (RMNH.MOL. 234,108), Cueva de Torcona, very long and broad, ibid. — Magnification varies for each perspective, see scale bars; all Figs imaged by M. Ruppel, (ret.) Goethe University Frankfurt am Main
Fig. 1 in Alveolar echinococcosis in nutria (Myocastor coypus), invasive species in Slovenia
Fig. 1. Pathomorphological finding in the liver of a nutria (Myocastor coypus) with echinococcosis. Numerous cysts of varying sizes on the surface of the liver (arrows). b Numerous fluid-filled cysts in the cut section of the liver. c Haematoxylin and eosin (HE) stain of single cyst with several protoscolices (black arrows). The cyst is lined by an eosinophilic, hyaline outer membrane (blue arrows) and an inner germinal epithelial layer. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
paperChain - Video Animation - Circular Case 3 (Slovenia)
<p>This animation video summarises in approximately two minutes the most relevant results of the implementation of paperChain's Circular Case.</p>
FIG. 4 in Where are we now? Early Medieval archaeozoology in Slovenia: an overview
FIG. 4. — Abundance of taxonomically identified animal remains per building area for: A, Buildings I, II; B, Buildings IV, VI at Pristava. Also given is the total abundance of taxonomically identified animal remains per taxa for the whole site (NISP Σ). The lists of micro-squares included in each building area are as follows (Pleterski 2010: fig. 5.5): Building I (micro-squares Su, Dr, Ni, Mo); Building II (micro-squares He, Po, Ba, RO); Building IV (micro-squares Mi, AI) and Building VI (micro-squares Šp, Pš, Ir, Ri). Only those specimens that could be reliably assigned to individual buildings are considered, which is why the data shown here differ slightly from those in Table 3.
FIG. 1 in Where are we now? Early Medieval archaeozoology in Slovenia: an overview
FIG. 1. — Geographical location of the study area. Also shown are the archaeological sites mentioned in the text.
FIG. 3 in Where are we now? Early Medieval archaeozoology in Slovenia: an overview
FIG. 3. — Individual building areas at Pristava as defined by Pleterski (2010: 165-167, 245, figs. 5.4, 5.5).
FIG. 2 in Where are we now? Early Medieval archaeozoology in Slovenia: an overview
FIG. 2. — Final distribution of the matrix derived from multidimensional scaling of Euclidean distances among 20 early medieval mammal assemblages from Slovenia (stress = 0.0268). Each assemblage is a random subsample of the total available archaeozoological data from the sites of:, Popava (N = 5);, Pristava (N = 5);, Tonovcov grad (N = 5);, Koper (N = 5). Subsample size is constant (NISP = 30).
Data from Commission for the Prevention of Corruption of the Republic of Slovenia: public-to-private transactions
<p>Public spending is often a contentious subject because different political parties have different agendas as to what should be the current national priorities. Of course, the same is true for the public in general. It is thus of interest to determine whether public spending is indeed as biased and capricious as it is often perceived, or whether there nevertheless exist some fundamental principles that guide it. We use data from the Commission for the Prevention of Corruption of the Republic of Slovenia, detailing every transfer of public money to the private sector from January 2003 to May 2020. During this time Slovenia has done business with no less than 248,989 companies. We find that the cumulative distribution of money received per company can be reasonably well explained by means of a power-law or a log-normal fit. We also show evidence for the first-mover advantage, and determine that the attachment rate of public spending to companies over time is roughly linear. These results indicate that Slovenian public spending is to a large extent guided by self organizing principles that, against all odds, go beyond nefarious interests and lobbying.</p>
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