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1,162 results for “fiber”
Abb. 5 in Verbreitung und Bestand des Europäischen Bibers (Castor fiber LINNAEUS, 1758) in der Steiermark (Österreich)
Abb. 5: Aktuelle Verbreitung des Bibers in der Steiermark. Auflösung 3x5 Minuten-Rasterfelder. Grafik: P. Zimmermann.
Abb. 16 in Verbreitung und Bestand des Europäischen Bibers (Castor fiber LINNAEUS, 1758) in der Steiermark (Österreich)
Abb. 16: Biberreviere im Einzugsgebiet der Lafnitz im Feistritztal sowie an der Ilz. Grafik: P. Zimmermann.
Abb. 6 in Verbreitung und Bestand des Europäischen Bibers (Castor fiber LINNAEUS, 1758) in der Steiermark (Österreich)
Abb. 6: Verteilung der Biberreviere in der Steiermark und deren Klassifizierung nach dem Reviertyp. Das Vorkommen an der Salza ist hier nicht berücksichtigt. Grafik: P. Zimmermann.
Abb. 3 in Verbreitung und Bestand des Europäischen Bibers (Castor fiber LINNAEUS, 1758) in der Steiermark (Österreich)
Abb. 3: Historische Verbreitung des Bibers in der Steiermark nach STÜBER (1988), verändert. Grafik: P. Zimmermann.
Abb. 14 in Verbreitung und Bestand des Europäischen Bibers (Castor fiber LINNAEUS, 1758) in der Steiermark (Österreich)
Abb. 14: Biberreviere im Einzugsgebiet der Lafnitz im Lafnitztal zwischen Hartberg und der Ortschaft Lafnitz. Grafik: P. Zimmermann.
Abb. 20-25 in Verbreitung und Bestand des Europäischen Bibers (Castor fiber LINNAEUS, 1758) in der Steiermark (Österreich)
Abb. 20-25: 20 (links oben): Biberburg an der Mur im Bereich der Aufweitungsstrecke bei Gosdorf, 30.12.2012; – 21 (rechts oben): Fällplatz am Lobenbach bei Neudau, 09.12.2013; – 22 (links mitte): Frassplatz an der Raab bei Fehring, 19.02.2013; – 23 (rechts mitte): Nagespuren an der Feistritz bei Fürstenfeld, 07.03.2013; – 24 (links unten): Wechsel in einen Maisacker an der Lassnitz bei Matzelsdorf, 11.01.2013; – 25 (rechts unten): Trittsiegel des Bibers an der Sulm bei Heimschuh, 28.02.2013. Fotos: B. Komposch.
Text-fig. 3 Ternary diagram of the relative abundance (in %) of juvenile, prime adult, and old adult specimens in samples of Castor fiber (data from Table 3). The red dots indicate the Pleistocene samples of Bilzingsleben II (B), Weimar- Ehringsdorf (E), and Weimar-Taubach (T), the black dot represents an extant population from Telemark in Norway (data from Campbell 2009). Abbreviations of zones (after Discamps and Costamagno 2015): JOP – Juveniles-Old-Prime dominated zone, JPO – Juveniles-Prime-Old dominated zone, O – Old dominated zone, P – Prime dominated zone. The diagram shows the position of all three fossil samples in the prime dominated zone. in Mortality Profiles Of Castor And Trogontherium (Mammalia: Rodentia, Castoridae), With Notes On The Site Formation Of The Mid-Pleistocene Hominin Locality Bilzingsleben Ii (Thuringia, Central Germany)
Text-fig. 3 Ternary diagram of the relative abundance (in %) of juvenile, prime adult, and old adult specimens in samples of Castor fiber (data from Table 3). The red dots indicate the Pleistocene samples of Bilzingsleben II (B), Weimar- Ehringsdorf (E), and Weimar-Taubach (T), the black dot represents an extant population from Telemark in Norway (data from Campbell 2009). Abbreviations of zones (after Discamps and Costamagno 2015): JOP – Juveniles-Old-Prime dominated zone, JPO – Juveniles-Prime-Old dominated zone, O – Old dominated zone, P – Prime dominated zone. The diagram shows the position of all three fossil samples in the prime dominated zone.
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i). in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 54. Scanning electron microscope (SEM; a–e, g, h) and synchrotron x-ray microscopy (SRXTM; f, i) images of unnamed angiosperm fruits and seeds; Torres Vedras locality, Portugal. a) Follicle sp. 1, narrow elongate follicle with sessile and decurrent stigma; b) Follicle sp. 2, broad, dehisced follicle with elongate and transverse fibers lining the locule; c) Angiosperm seed sp. 1 with thin, smooth seed coat; d) Angiosperm seed sp. 2 with verrucate seed coat; e) Angiosperm seed sp. 3 with exotestal and foveolate seed coat; f) Angiosperm seed sp. 4 with smooth seed coat; g, h) Angiosperm seed sp. 5 with raised epidermal cells forming a reticulate pattern; i) Wedge-shaped angiosperm fruit with remains of floral parts near apex. Specimens, TV43-S136726 (a), TV44-S148144 (b), TV43-S170074 (c), TV43-S136747 (d), TV43-S170073 (e), TV38-S174615 (f), TV44-S148003 (g), TV44-S148004 (h), TV43-S174685 (i). Scale bars 300 Μm (a–i).
Text-fig. 4. Scanning electron microscope (SEM) images of megaspores with possible affinities to Selaginellales; Torres Vedras locality, Portugal. a, b) Hughesisporites galericulatus, lateral view of megaspore (a) with almost smooth surface and spore wall of thin elements forming a dense reticulum (b); c) Trileites sp., proximal view of megaspore with almost smooth surface and raised trilete mark; d–f) Rugotriletes sp., proximal (e) and lateral (f) views of megaspores showing coarsely reticulate-rugulate surface ornamentation and prominent gula around the trilete mark and compact perforate spore wall (d); g, h) Erlansonisporites sp., distal (g) and lateral (h) views of megaspores showing coarsely reticulate-rugulate surface and fibrous spore wall; i, j) Striatriletes sp. 1, megaspore in oblique proximal view (i) showing raised laesurae and irregular striate-rugulate surface, and detail of spore wall (j) showing dense packing of sculptural elements; k, l) Striatriletes sp. 2, megaspore in proximal view (k) showing trilete mark, striate-rugulate surface, and detail of spore wall (l) composed of loosely packed fibers; m) Striatriletes sp. 3, megaspore in proximal view showing raised trilete mark and striate-rugulate surface; n, o) Verrutriletes sp., megaspore in oblique proximal view (n) showing short laesurae of the trilete mark, and the dense verrucate surface (o); p) Megaspore sp. 1, oblique proximal view showing in The Early Cretaceous Mesofossil Flora Of Torres Vedras (Ne Of Forte Da Forca), Portugal: A Palaeofloristic Analysis Of An Early Angiosperm Community
Text-fig. 4. Scanning electron microscope (SEM) images of megaspores with possible affinities to Selaginellales; Torres Vedras locality, Portugal. a, b) Hughesisporites galericulatus, lateral view of megaspore (a) with almost smooth surface and spore wall of thin elements forming a dense reticulum (b); c) Trileites sp., proximal view of megaspore with almost smooth surface and raised trilete mark; d–f) Rugotriletes sp., proximal (e) and lateral (f) views of megaspores showing coarsely reticulate-rugulate surface ornamentation and prominent gula around the trilete mark and compact perforate spore wall (d); g, h) Erlansonisporites sp., distal (g) and lateral (h) views of megaspores showing coarsely reticulate-rugulate surface and fibrous spore wall; i, j) Striatriletes sp. 1, megaspore in oblique proximal view (i) showing raised laesurae and irregular striate-rugulate surface, and detail of spore wall (j) showing dense packing of sculptural elements; k, l) Striatriletes sp. 2, megaspore in proximal view (k) showing trilete mark, striate-rugulate surface, and detail of spore wall (l) composed of loosely packed fibers; m) Striatriletes sp. 3, megaspore in proximal view showing raised trilete mark and striate-rugulate surface; n, o) Verrutriletes sp., megaspore in oblique proximal view (n) showing short laesurae of the trilete mark, and the dense verrucate surface (o); p) Megaspore sp. 1, oblique proximal view showing
A river on fiber: high resolution fluvial monitoring with distributed acoustic sensing – Data, Matlab Scripts and App
<p>Matlab software and data associated with Roth et al. (submitted to Seismica, 2025).</p>
Simultaneous dynamic glucose-enhanced (DGE) MRI and fiber photometry measurements of glucose in the healthy mouse brain
<p>This dataset was acquired for the DGE and fiber photometry study published in NeuroImage ( <a href="https://doi.org/10.1016/j.neuroimage.2022.119762">https://doi.org/10.1016/j.neuroimage.2022.119762</a>).<br> Comprises of three datasets: DGE MRI, fiber photometry and two-photon microscopy.</p>
Uptime data for 'Coherent fiber links operated for years: effect of missing data'
<p>Data of the total uptime of the comparison between two clocks, used in figure 13, in the article "Coherent fiber links operated for years: effect of missing data", doi: 10.1088/1681-7575/ac938e,.</p>
Text-fig. 19. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–c) of Aristospermum huberi and scanning electron microscope (SEM, d, e) images of Choffaticarpus compactus; Catefica locality, Portugal. a) Volume rendering of strongly flattened, triangular seed with pointed micropylar region; note thin-walled cells of outer integument preserved along the margins of the seed and pitted surface of the crystalliferous inner cells of outer integument where the outer cells are abraded and the narrow, lateral funicle/raphe; b) Volume rendering of seed showing surface of inner integument (endotesta) with cells showing clear imprints of crystals (arrows); c) Longitudinal section (orthoslice yz0241) of seed showing crystalliferous cells of endotesta (white arrows) and the two fiber layers of the tegmen that are perpendicular to each other (inner integument, ii-f, black arrows); d) Fragment of multiparted, apocarpous fruiting structure showing several helically-arranged, laterally flattened, fruitlets; e) Fruitlet in lateral view showing the prominent ventral face with its lateral groove, short attachment scar, and sunken regions of the fruit wall that indicate the probable presence of oil cells. Specimens, Catefica 49-S266049 (a–c), Catefica 49-S172558 (d), Catefica 49-S118675 (e). Scale bars = 300 Μm (a, c–e), 100 Μm (b). in The Early Cretaceous Mesofossil Flora Of Catefica, Portugal: Angiosperms
Text-fig. 19. Synchrotron radiation X-ray tomographic microscopy (SRXTM, a–c) of Aristospermum huberi and scanning electron microscope (SEM, d, e) images of Choffaticarpus compactus; Catefica locality, Portugal. a) Volume rendering of strongly flattened, triangular seed with pointed micropylar region; note thin-walled cells of outer integument preserved along the margins of the seed and pitted surface of the crystalliferous inner cells of outer integument where the outer cells are abraded and the narrow, lateral funicle/raphe; b) Volume rendering of seed showing surface of inner integument (endotesta) with cells showing clear imprints of crystals (arrows); c) Longitudinal section (orthoslice yz0241) of seed showing crystalliferous cells of endotesta (white arrows) and the two fiber layers of the tegmen that are perpendicular to each other (inner integument, ii-f, black arrows); d) Fragment of multiparted, apocarpous fruiting structure showing several helically-arranged, laterally flattened, fruitlets; e) Fruitlet in lateral view showing the prominent ventral face with its lateral groove, short attachment scar, and sunken regions of the fruit wall that indicate the probable presence of oil cells. Specimens, Catefica 49-S266049 (a–c), Catefica 49-S172558 (d), Catefica 49-S118675 (e). Scale bars = 300 Μm (a, c–e), 100 Μm (b).
Experimental data of Mg WE43 fiber biocorrosion in simulated body fluid
<p>This dataset contains the experimental data used to plot Figures 4 and 6 in the paper:</p> <p>S. Kovacevic, W. Ali, E. Martínez-Pañeda, J. LLorca “Phase-field modeling of pitting and mechanically-assisted corrosion of Mg alloys for biomedical applications” published in Acta Biomaterialia (2023)</p>
WIPP_BATS1_Temperature_Fiber
<p> </p> <p>This dataset includes the temperature fiber-optic monitoring data, ERT resistivity data, and thermal couple data from the ERT borehole from BATS 1 conducted at WIPP. The measurements cover the heating cycle from 01/21/2020 to 02/15/2020.</p> <p><a href="https://zenodo.org/api/files/609ce53c-a54d-4adc-8597-9a074afd82a3/WIPP%20Heater__2019-12-17_23-00-16%20%281%29_ch1_full.tsv">WIPP Heater__2019-12-17_23-00-16 (1)_ch1_full.tsv </a>and <a href="https://zenodo.org/api/files/609ce53c-a54d-4adc-8597-9a074afd82a3/WIPP%20Heater__2019-12-17_23-00-16%20%281%29_ch3_full.tsv">WIPP Heater__2019-12-17_23-00-16 (1)_ch3_full.tsv </a>are from the 5-m long fiber-optic borehole and the 10-m long fiber-optic borehole, respectively.</p> <p><a href="https://zenodo.org/api/files/609ce53c-a54d-4adc-8597-9a074afd82a3/Array_Heated_Temperature_SN7066_Data_v2.xlsx">Array_Heated_Temperature_SN7066_Data_v2.xlsx </a> is the thermal couple data in the ERT borehole.</p> <p><a href="https://zenodo.org/api/files/609ce53c-a54d-4adc-8597-9a074afd82a3/P1_1.csv">P1_1.csv</a>, <a href="https://zenodo.org/api/files/609ce53c-a54d-4adc-8597-9a074afd82a3/P1_1.csv">P1_2.csv</a>, and <a href="https://zenodo.org/api/files/609ce53c-a54d-4adc-8597-9a074afd82a3/P1_1.csv">P1_3.csv </a>are the resistivity data from three different depths: top (1.7 m from the drift wall), mid (2.9 m from the drift wall), and bottom (4.1 m from the drift wall).</p> <p> </p>
Azcorra2023 - Histological images for fiber placement localization
<p>Microscopy images of coronal mouse brain slices used for localization of fiber placement in striatum after acute fiber photometry experiments, as used in Azcorra et al. Nat Neuro 2023.</p>
Dataset for "Suppressing transverse mode instability through multimode excitation in a fiber amplifier"
<p>Numerical and theoretical data associated with "Suppressing transverse mode instability through multimode excitation in a fiber amplifier" (doi.org/10.1073/pnas.2217735120). </p>
Supporting data for "Detection of single ions in a nanoparticle coupled to a fiber cavity"
<p>Data for Fig. 2b, 2d, 3 and 4 of the paper "Detection of single ions in a nanoparticle coupled to a fiber cavity"</p>
Soil temperature profiles, measured using a coil-shaped fiber-optic distributed temperature sensor
<p>Measurements of soil temperature temperature profile, by reference sensors and a coil-shaped fiber optic distributed temperature sensor.</p> <p>Retrieved at the Speulderbos measurement site, 52.251048 N, 5.690061 E.</p> <p> </p> <p>A full description can be found in:</p> <p>Schilperoort, B. (2022). <em>Heat Exchange in a Conifer Canopy: A Deep Look using Fiber Optic Sensors</em> [Delft University of Technology]. https://doi.org/10.4233/uuid:6d18abba-a418-4870-ab19-c195364b654b</p>
Climbing fiber multi-innervation of mouse Purkinje dendrites with arborization common to human
<p>Canonically, each Purkinje cell in the adult cerebellum receives only one climbing fiber from the inferior olive. Underlying current theories of cerebellar function is the notion that this highly conserved one-to-one relationship renders Purkinje dendrites into a single computational compartment. However, we show that multiple primary dendrites are a near-universal morphological feature in humans. Using tract-tracing, immunolabeling, and in vitro electrophysiology, we demonstrate in mice that ~25% of mature polydendritic cells receive more than one climbing fiber input. Two-photon calcium imaging in vivo reveals that separate dendrites can exhibit distinct response properties to sensory stimulation, indicating some polydendritic cells integrate functionally independent climbing fiber receptive fields. These findings reveal that Purkinje cells are morphologically and functionally more diverse than previously thought.</p>
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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.
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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.
OpenNeuro
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