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83 results for “southern Poland”
Manually Annotated Drone Imagery (RGB) Dataset for automatic coastline delineation of Southern Baltic Sea, Poland with polyline annotations (0.1.1)
<p><strong>Overview:</strong></p> <p>The Manually Annotated Drone Imagery Dataset (MADRID) consists of hand annotated high resolution RGB images taken in two different types of coasts in Poland, Miedzyzdroje - cliff coast and in Mrzezyno - dune coast in 2022-2023. All images were converted into a uniform format of 1440x2560 pixels, polyline annotated and set into file structure format suited for semantic segmentation tasks (See "Usage" notes below for more details).</p> <p>The raw images of our dataset were captured Zenmuse L1 Sensor (RGB) mounted on a DJI Matrice 300 RTK Drone. Total of 4895 images were captured, however the dataset contains 3876 images with each image annotated with coastline. The dataset only include images with coastlines that are visually identifiable with the human eye. For the annotations of the images, CVAT v2.13 open-source software was utilized.</p> <p><strong>Usage:</strong></p> <p>The compressed RAR file contains two folders train and test. Each folder contains the file that represents the date at which the image was captured in the format of (year, month, day), number of the image and the name of the drone utilized to capture the image. For example, DJI_20220111140051_0051_Zenmuse-L1-mission and DJI_20220111140105_0053_Zenmuse-L1-mission. Additionally, the test folder contains annotations (one per image) which are extracted from the original XML annotation file provided in the CVAT 1.1 image format.</p> <p>Archives were compressed using RAR compression. They can be decompressed in a terminal by opening and extracting Madrid_v0.1_Data.zip.</p> <p>The subset of the data with the name Madrid_subset_data.zip has been added which contains a small portion of train and test images for purpose of inspecting the dataset without downloading the entire dataset.</p> <p>The training images for both training data and testing data are structured as follows.</p> <pre><code>Train/ └── images/ └── DJI_20220111140051_0051_Zenmuse-L1-mission.JPG └── DJI_20220111140105_0053_Zenmuse-L1-mission.JPG └── ...<br>└── masks/ └── DJI_20220111140051_0051_Zenmuse-L1-mission.PNG └── DJI_20220111140105_0053_Zenmuse-L1-mission.PNG └── ...<br><br>Test/ └── images/ └── DJI_20220111140051_0051_Zenmuse-L1-mission.JPG └── DJI_20220111140105_0053_Zenmuse-L1-mission.JPG └── ...<br>└── masks/ └── DJI_20220111140051_0051_Zenmuse-L1-mission.PNG └── DJI_20220111140105_0053_Zenmuse-L1-mission.PNG └── ...</code></pre> <p> </p>
Figure 2 in Comparison of the species composition of Gamasina mite communities (Acari: Mesostigmata) in selected caves of the Kraków-Cz stochowa Upland (southern Poland) and their immediate surroundings
Figure 2. Diagram of the correspondence analysis (CA) for the sampling sites. The diagram shows only the most important species (for abbreviations see Table 1).
Fig. 1 in A Long-Term Comparison Of Laying Date And Clutch Size In The Red-Backed Shrike (Lanius Collurio) In Silesia, Southern Poland
Fig. 1. The number of Red-backed Shrike clutches laid during successive five-day periods (1 = 6–10 May) in the two study periods. For sample size – see text
FIGURE 5 in A reconsideration of the palinuroid family Synaxidae (Crustacea, Decapoda), with a new member from the Upper Jurassic of southern Poland
FIGURE 5. Palinuroid evolutionary scenario proposed herein, combining data from Holthuis (1991), Haug et al. (2009), and present observations of Palaeosynaxes montserratae nov. gen., nov. sp.
FIGURE 3 in A reconsideration of the palinuroid family Synaxidae (Crustacea, Decapoda), with a new member from the Upper Jurassic of southern Poland
FIGURE 3. Distribution of synaxid achelatans over geological time, from the Late Jurassic to the present day. A, Extant Palinurellus gundlachi von Martens, 1878. B, Extant Palinurellus wienecki (De Man, 1881). C, Extant Palibythus magnificus Davie, 1990. D, Late Eocene Palinurellus bericus De Angeli and Garassino, 2014. E, Late Cretaceous (Cenomanian) Palaeopalinurellus jbeilensis Garassino and Pasini, 2020. F, Late Jurassic (Tithonian) Palaeopalinurellus strambergensis (Bachmayer, 1959). G, Late Jurassic (Oxfordian) Palaeopalinurellus culocervus Fraaije, Van Bakel, Jagt, and Brochet, 2020.
FIGURE 4 in A reconsideration of the palinuroid family Synaxidae (Crustacea, Decapoda), with a new member from the Upper Jurassic of southern Poland
FIGURE 4. Palaeosynaxes montserratae nov. gen., nov. sp., holotype (MAB k3781), in left lateral and dorsal views, scale bar equals 5 mm.
FIGURE 2 in A reconsideration of the palinuroid family Synaxidae (Crustacea, Decapoda), with a new member from the Upper Jurassic of southern Poland
FIGURE 2. Sedimentology, palaeoecology, and presence of decapod crustaceans in the Szklarka valley outcrop (see Figure 1 after Müller et al., 2000; supplemented by Fraaije et al., 2022). The black star denotes the approximate level of provenance of the holotype of Palaeosynaxes montserratae nov. gen., nov. sp. (Figure 4).
FIGURE 1 in A reconsideration of the palinuroid family Synaxidae (Crustacea, Decapoda), with a new member from the Upper Jurassic of southern Poland
FIGURE 1. Lithostratigraphical column of Oxfordian strata in the Kraków area (southern Poland), with indication of the Szklarka valley locality (modified after Matyszkiewicz, 1996; Matyszkiewicz et al., 2012).
Fig. 1 in Beetles (Coleoptera) from seaside beach and dunes in the regions of Świnoujście, Międzyzdroje and Wisełka (Poland) located along the southern coast of the Baltic Sea
Fig. 1. The examined seaside beach and dunes in the regions of Świnoujście, Międzyzdroje and Wisełka.
Fig. 4 in A new occurrence of the Late Triassic archosaur Smok in southern Poland
Fig. 4. Predatory archosaurs from Late Triassic of Poland, Smok sp., Marciszów near Zawiercie (A, B) and Smok wawelski Niedźwiedzki, Sulej, and Dzik, 2012, Lipie Śląskie clay-pit at Lisowice (C–E). A. Distal part of the right pubis, pubic "boot" (WNoZ/S/7/170), in lateral (A1), medial (A2), ventral (A3), and dorsal (A4) views. B. Middle part of the left ischium shaft (WNoZ/S/7/168), in lateral (B1), dorsal (B2), and medial (B3) views. C. Left ischium (ZPAL V.33/302), in lateral view. D. Reconstruction of right pubis in lateral view; based on specimens ZPAL V.33/311A, B and ZPAL V.33/298 (from Niedźwiedzki 2013). E. Distal part of the right pubis, pubic "boot" (ZPAL V.33/298), in medial (E1) and lateral (E2) views. Scale bars 10 mm.
Fig. 3 in A new occurrence of the Late Triassic archosaur Smok in southern Poland
Fig. 3. Predatory archosaurs from Late Triassic of Poland, Smok sp., Marciszów near Zawiercie (A) and Smok wawelski Niedźwiedzki, Sulej, and Dzik, 2012, Lipie Śląskie clay-pit at Lisowice (B). A. Fragment of proximal region of the right femur (WNoZ/S/7/160), in anterior (A1) and posterior (A2) views, distal cross section (A3). B. Left femur (ZPAL V.33/45) in anteromedial view. Scale bars 10 mm.
Fig. 5 in A new occurrence of the Late Triassic archosaur Smok in southern Poland
Fig. 5. Comparison and details of articular surface of the mid-dorsal vertebrae (in posterior view) of the predatory archosaurs from Late Triassic of Poland. A. Smok sp. (WNoZ/S/7/199), Marciszów near Zawiercie. B. Smok wawelski Niedźwiedzki, Sulej, and Dzik, 2012 (ZPAL V.33/42), Lipie Śląskie clay-pit at Lisowice. Scale bars 10 mm.
Fig. 1. A in A new occurrence of the Late Triassic archosaur Smok in southern Poland
Fig. 1. A. Geological map of the Silesia showing location of the Marciszów site (asterisk), where the Smok sp. fossil remains were discovered (modified from Niedźwiedzki et al. 2014). B. The schematic section of the Marciszów site; arrows indicate two horizons suspected as being provenance of the bones; modified from Budziszewska-Karwowska et al. 2010). C, D. Maps (C, simplified plan of Marciszów; D, satellite map of the area from Google Earth®) showing position of the bone-bearing rock pile. Abbreviations: b/c, breccia and conglomerate; mu, mudstone; s, sandstone; si, siltstone.
Fig. 9. A in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 9. A phylogeny of diapsids with the main transitions of the fifth metatarsal mapped onto it (based on Benton 1985; Evans 1988; Gauthier et al. 1988a; Sereno 1991; Dilkes 1998; Ezcurra et al. 2014). 1, plesiomorphic state; 2, diapsid synapomorphy: foot integration; 3, saurian synapomorphy: neckless hooked MttV; 4, long-necked hooked MttV; 4', lepidosaurian synapomorphy: dorso-ventral inflexion of the long-necked hooked MttV; 5, ornithodiran synapomorphy: MttV straight, reduced in size and importance.
Fig. 8 in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 8. Schematic relations between distal tarsals and metatarsals in diapsids and their out-group. A. Captorhinus, basal Amniota, Early Permian, North America (after Heaton and Reisz 1982). B. Petrolacosaurus, basal Diapsida, Late Carboniferous, North America (after Reisz (1981). C. Saurosternon, basal Diapsida, Late Permian South Africa (after Carroll 1975). D. Protorosaurus, Archosauromorpha, Late Permian, Germany and England (after Gottmann-Quesada and Sander 2009). E. Boreopricea, Early Triassic, Northern Russia (after Benton and Allen 1997). F, G. Macrocnemus, Middle Triassic, Italy (after Rieppel 1989: fig. 8D, F, respectively). H. Prolacerta, Archosauromorpha, Early Triassic, South Africa (after Gow 1975). I. Pamelaria, Archosauromorpha, Middle Triassic, India (after Sen 2003). J. Mesosuchus, Rhynchosauridae, Early–Middle Triassic, South Africa (after Dilkes 1998). K. MttV morphotype X, Early Triassic. Poland. L. MttV of Sophineta, Early Triassic. Poland. M. MttV of Gephyrosaurus, Lepidosauromorpha, Early Jurassic, UK (after Evans 1981). A–M all in plantar view. dTIV, MttIV and MttV. dTIV, MttIV, and MttV shaded in grey. 1 , plesiomorphic state; 2, diapsid synapomorphy: foot integration; 3, saurian synapomorphy: neckless hooked MttV; 4, long-necked hooked MttV; 4', lepidosaurian synapomorphy: dorso-ventral inflexion of the long-necked hooked MttV. Not to scale.
Fig. 7 in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 7. Schematic relations between distal tarsals and metatarsals in Archosauriformes. A. Erythrosuchus, Erythrosuchidae, Early Triassic, Africa (after Gower 1996). B. Euparkeria, Euparkeriidae, Middle Triassic South Africa after Ewer 1965). C. Riojasuchus, Crurotarsi, Late Triassic South America after Sereno 1991). D. Rhamphorhynchus, Pterosauria, Late Jurassic, Europe, Africa (after Wellnhofer 1991). E. Pteranodon, Pterosauria, Late Cretaceous, North America (after Bennett 2001). F. Scleromochlus, Ornithodira, Late Triassic, England (after Benton 1999). G. Marasuchus, Dinosauriformes, Middle Triassic, South America (after Sereno and Arcucci 1994). Dorsal (A, B) and plantar (C, G) views. dTIV, MttIV and MttV shaded in grey. 3, saurian synapomorphy: neckless hooked MttV; 5, ornithodiran synapomorphy: MttV straight, reduced in size and importance. Not to scale.
Fig. 5. Sauria indet. morphotype X in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 5. Sauria indet. morphotype X from the Lower Triassic of Czatkowice, southern Poland. A. ZPAL RV/1991, adult left MttV in plantar (A1) and lateral-slightly plantar (A2) views. B. ZPAL RV/1354, juvenile left MttV in medial (B1) and plantar (B2) views. C. ZPAL RV/1992, adult left MttV in dorsal view. SEM stereo-pairs.
Fig. 4 in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 4. Lepidosauromorph saurian Sophineta cracoviensis Evans and Borsuk-Białynicka, 2009 (A, B) and morphotype Y (C) from the Lower Triassic of Czatkowice, southern Poland and Macrocnemus bassani (Nopcsa, 1930) (D, E) from the Middle Triassic of Switzerland. A. ZPAL RV/1990, left MttV in dorsal (A1) and medial (A2) views. B. ZPAL RV/1353, right MttV in plantar (B1) and lateral (B2) views. C. ZPAL RV/1989, left MttV in plantar view. D. PIMZ T 2816, left MttV (reversed) in plantar view. E. PIMZ T 2472, right MttV in plantar view. A–C, SEM stereo-pairs. D, E not to scale, after Rieppel (1989: fig. 8B, E).
Fig. 3 in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 3. Archosauriform Osmolskina czatkowicensis Borsuk-Białynicka and Evans, 2003 (A, B) and Archosauriformes gen. et sp. indet (C) all from the Lower Triassic Czatkowice locality, Poland. A. ZPAL RV/1347, adult, left MttV in plantar view. B. PAL RV/1346, young adult, right MttV in medial (B1), lateral (B2), and dorsal (B3) views. B1, B2, reversed. C. ZPAL RV/1993, right MttV in dorsal view. SEM photographs; A, B, stereo-pairs.
Fig. 2 in Diversity of diapsid fifth metatarsals from the Lower Triassic karst deposits of Czatkowice, southern Poland -functional and phylogenetic implications
Fig. 2. Comparison of fifth metatarsal architecture. Right bones in lateral view (A, B, C1, D, E2, F2) and in medial view (C2, E1, F1). A. Iguana iguana (Linnaeus, 1758), Iguanidae, Recent. B. Sphenodon punctatus (Gray, 1842), Rhynchocephalia, Recent. C. Sophineta cracoviensis Evans and BorsukBiałynicka, 2009, Lepidosauromorpha, Early Triassic, Poland. D. Gephyrosaurus bridensis Evans, 1980, Rhynchocephalia, Early Jurassic, South Wales, UK; straight line approximates not-inflacted shape of the MttV. E. Morphotype X, Early Triassic, Poland (left MttV reversed). F. Osmolskina czatkowicensis Borsuk-Białynicka and Evans, 2003, Archosauriformes, Early Triassic, Poland. inf, inflection angle. Not to scale. A, B after Robinson (1975); D, after Evans (1981).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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.