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612 results for “Croatia”
Fig. 2 in Body Measurements And Harversting Dynamics Of The Fat Dormouse (Glis Glis L.) In The Mountainous Part Of Croatia
Fig. 2. Trends in harvesting the fat dormouse (Glis glis L.) in the municipalities of Gerovo (1), Tršće (2) and Prezid (3) between 1991 and 2001
Figure 4. A cove with shallow water near Ponte Porton with 14 in Populations of Microcondylaea bonellii (Férussac 1827), Unionidae - an european freshwater mussel at rapid decline - and Unio mancus in Istria, Croatia
Figure 4. A cove with shallow water near Ponte Porton with 14 individuals of Microcondylaea bonellii (26.9.2009).
Figure 3 in Populations of Microcondylaea bonellii (Férussac 1827), Unionidae - an european freshwater mussel at rapid decline - and Unio mancus in Istria, Croatia
Figure 3. Numbers of shells of Unio mancus (blue) and Microcondylaea bonelli at the different sites (red).
Fig. 2 and 3 in Populations of Microcondylaea bonellii (Férussac 1827), Unionidae - an european freshwater mussel at rapid decline - and Unio mancus in Istria, Croatia
Fig. 2 and 3 give the results of my surveys in river Mirna in 2009 to 2016. In the upper part of the river from the city of Buzet to the confluence with Butoniga the artificially straightened riverbed is dominated by coarse gravel and shows ± rapid current. Although Microcondylaea was recorded from this part of the river near Istarske Teplice (Fischer 1999) no shells or living specimens were found actually. Populations of Unio mancus were mainly found in tributaries like Bračana and drenches, less frequently in the riverbed of upper Mirna. Between 2009 and 2016 the Mirna-riverbed was reconstructed in several places, eroded banks with coves and fine sand substrate were replaced by blocks of stone and the riverbed straightened again. Thus many suitable habitats and eventually existing mussels-populations were destroyed, so much the worse as heavy machines were driving in the riverbed over many weeks for the construction works and mobilized the substrate, which led to high accumulations of fine sediment in the lower part of the river, especially in parts with low current and coves which were inhabited by Microcondylaea.
Figure 1 in Populations of Microcondylaea bonellii (Férussac 1827), Unionidae - an european freshwater mussel at rapid decline - and Unio mancus in Istria, Croatia
Figure 1. Map of known living populations of Microcondylaea bonelli in Slovenia (grey) and Italy (yellow) from http://art17.eionet.europa.eu/article17/reports2012/species/summary/. Populations in Croatia (red) added by the author.
◂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. 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
Figures 9–16 - Neobisium curcici n in On the biodiversity of pseudoscorpions in Croatia: Neobisium curcici (Pseudoscorpiones: Neobisiidae), a new cave-dwelling species from Dalmatia (Croatia)
Figures 9–16 - Neobisium curcici n. sp., paratype tritonymph from the Jama pod Gažnovcem Pit, Stilja, near Vrgorac, Dalmatia, Croatia: 9 – carapace; 10 – epistome; 11 – chelicera; 12 – sternites II-IV; 13 – flagellum; 14 – pedipalp; 15 – pedipalpal chela; 16 – leg IV. Scale = 0.50 mm (Figs. 9, 14–16) and 0.25 mm (Figs. 10–13).
Figure 5 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 5. Maximum likelihood phylogram based on a fragment of COI (DNA barcode region) showing the related relationships of the genus Glossosoma. The bootstrap values (BS) are marked on the branches in the order NJ/ML. BS values less than 80 are not shown. The groups delineated by ABGD approach are shown on the right side of the tree. Specimens which genomic DNA was extracted in this study are written in bold letter.
Figure 1 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 1. Map of the study area with sampling stations. Names and corresponding abbreviations of the stations are listed in Table 1.
Figure 3 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 3. MDS analysis of caddisfly fauna similarity at stations on the Cetina, the Ruda, the Grab and the Rumin rivers.
Figure 2 in Biodiversity, DNA barcoding data and ecological traits of caddisflies (Insecta, Trichoptera) in the catchment area of the Mediterranean karst River Cetina (Croatia)
Figure 2. Cluster analysis of caddisfly fauna similarity at stations on the rivers Cetina, Ruda, Grab and Rumin.
Figure 4 in First DNA barcoding of a new alien species Glycaspis brimblecombei Moore, 1964 (Hemiptera: Aphalaridae) in Croatia with a distribution note
Figure 4. Neighbor-joining phylogenetic tree constructed by sequences of the mtCOI-3P of Glycaspis brimblecombei Lokrum, Croatia of Glycaspis species from BOLD and GenBank databases, based on Kimura-2-parameter distance model. Numbers at nodes are NJ bootstrap support values calculated from 2000 bootstrap replicates.
Figure 1 in First DNA barcoding of a new alien species Glycaspis brimblecombei Moore, 1964 (Hemiptera: Aphalaridae) in Croatia with a distribution note
Figure 1. Distribution of species Glycaspis brimblecombei. A. Spread of the species G. brimblecombei. The coloration of the lines shows the spread of the species in the temporal scale (excluding localities for which the year of occurrence of the species is not known), B. and C. Location of sampling – Botanical Garden of the Institute for Marine and Coastal Research on the island of Lokrum.
Figure 3 in First DNA barcoding of a new alien species Glycaspis brimblecombei Moore, 1964 (Hemiptera: Aphalaridae) in Croatia with a distribution note
Figure 3. Developmental stages of Glycaspis brimblecombei: A. lerps, nymphs and egg cluster, B. adult (scale: 1 mm).
Figure 5 in Ecological and faunistic features of caddisflies (Insecta: Trichoptera) in different types of habitats in the Dinaric karst area (Central Croatia)
Figure 5. Maximum likelihood (ML) phylogram based on 658 bp long fragment of the mt COI DNA barcode region showing the relationships between species of the genus Setodess. Numbers above the branches represent bootstrap support (BS) for Neighbor-Joining (NJ) and ML analysis (NJ/ML). BS values less than 60 are not shown. Specimen ID from sequences obtained in this study are written with bold letters.
Figure 3 in Ecological and faunistic features of caddisflies (Insecta: Trichoptera) in different types of habitats in the Dinaric karst area (Central Croatia)
Figure 3. NMDS similarity analysis of caddisflies fauna at the study area (sampling sites correspond to the list in Tab. 1).
Figure 2 in Ecological and faunistic features of caddisflies (Insecta: Trichoptera) in different types of habitats in the Dinaric karst area (Central Croatia)
Figure 2. Dobra - spring (D1), Dobra - upper Dobra (D2), Dobra - canyon (D4), Kamačnik - spring (K1), Zagorska Mrežnica - spring (ZM), Sabljaci - reservoir (SR).
Figure 4 in A surprising finding of Ecclisopteryx asterix Malicky, 1979 (Insecta, Trichoptera) in Croatia with notes to DNA barcoding and new distributional data of the subfamily Drusinae
Figure 4. Spatial distribution of the Drusinae species in Croatia, literature data supplemented with new records.
Figure 3 in A surprising finding of Ecclisopteryx asterix Malicky, 1979 (Insecta, Trichoptera) in Croatia with notes to DNA barcoding and new distributional data of the subfamily Drusinae
Figure 3. Maximum likelihood phylogram based on the COI sequences of Ecclisopteryx asterix from Croatia and haplotypes of Ecclisopteryx species available in BOLD database. Numbers at the nodes indicate maximum likelihood (ML) bootstrap support values (BS). Terminal codes represent BOLD Process IDs.
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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.