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767 results for “switzerland”
Subspecies and Distribution. C.g.gueldenstaedtiiPallas,1811—SEuropeanRussia(WCaucasus),Georgia,Armenia,Azerbaijan,Turkey,WIran,Syria,Iraq,Lebanon,Israel,Jordan,Egypt(Sinai),andsomeMediterraneanIs,includingCrete,Corsica,andMinorcaintheBalearicIs;itmightoccurinSaudiArabia. C.g.cypriaBate,1903—Cyprus. C.g.iculismaMottaz,1908—N&WIberianPeninsula,SFrance,SarkI(ChannelIs),andNWItaly. C. g. mimula G. S. Miller, 1901 — Europe (from NW France, Switzerland, and N Italy E to W Ukraine and Balkan Peninsula). in Soricidae
Subspecies and Distribution. C.g.gueldenstaedtiiPallas,1811—SEuropeanRussia(WCaucasus),Georgia,Armenia,Azerbaijan,Turkey,WIran,Syria,Iraq,Lebanon,Israel,Jordan,Egypt(Sinai),andsomeMediterraneanIs,includingCrete,Corsica,andMinorcaintheBalearicIs;itmightoccurinSaudiArabia. C.g.cypriaBate,1903—Cyprus. C.g.iculismaMottaz,1908—N&WIberianPeninsula,SFrance,SarkI(ChannelIs),andNWItaly. C. g. mimula G. S. Miller, 1901 — Europe (from NW France, Switzerland, and N Italy E to W Ukraine and Balkan Peninsula).
Subspecies and Distribution. S.a.alpinusSchinz,1837—SEFrance,Switzerland,NItaly,C&SGermany,SWCzechRepublic,Austria,Slovenia,NWHungary,Croatia,BosniaandHerzegovina,Serbia,Montenegro,andNAlbania. S.a.hercynicusG.S.Miller,1909—NGermany(Harz);possiblyextinct. S. a. tatricus Kratochvil & Rosicky, 1952 — N & E Czech Republic, Slovakia, S Poland, W Ukraine, NE Hungary, and Romania. in Soricidae
Subspecies and Distribution. S.a.alpinusSchinz,1837—SEFrance,Switzerland,NItaly,C&SGermany,SWCzechRepublic,Austria,Slovenia,NWHungary,Croatia,BosniaandHerzegovina,Serbia,Montenegro,andNAlbania. S.a.hercynicusG.S.Miller,1909—NGermany(Harz);possiblyextinct. S. a. tatricus Kratochvil & Rosicky, 1952 — N & E Czech Republic, Slovakia, S Poland, W Ukraine, NE Hungary, and Romania.
AI results complementing the 2021 Annual Report on surveillance for Avian Influenza in poultry and wild birds in Member States of the European Union - Switzerland
<p>This dataset contains the results of the surveillance activities conducted in 2021, which consisted of:</p> <ul> <li>Serological surveys to monitor the circulation of AIV subtypes H5 and H7 in poultry (active surveillance). These surveys should preferentially target poultry species or production systems with increased risk for introduction of avian influenza (AI).</li> <li>Passive surveillance aiming at the virological detection of AI in wild birds found dead or moribund</li> </ul>
Dataset for "Emerging tremors and increasing seismic noise precede micro-earthquakes triggered in a fluid-activated shale fault slip experiment (2015, Mt Terri URL, Switzerland)"
<p>This dataset contains the raw data of the injection experiment, performed in the Mt Terri Underground Platform in 2015 and used in the article:</p> <p><strong>De Barros, L., </strong>Guglielmi, Y., F. Cappa, C. Nussbaum, J. Birkholzer, 2023. Induced microseismicity and tremor signatures illuminate different slip behaviors in a natural shale fault reactivated by a fluid pressure stimulation (Mont Terri), <em>Geophysical Journal International</em>, 10.1093/gji/ggad231<br> <br> From a horizontal gallery, three vertical boreholes allowed the deployment of an injection probe (called SIMFIP; Guglielmi et al., 2014) and the monitoring sensors in the upper compartment of a N50°-60°SE fault zone. The 2.4 m long injection chamber of the SIMFIP probe was centered at 340.6 m depth, where a 3D displacement sensor was anchored on the borehole walls. A second SIMFIP probe is located 3.1 m northwest of the injection at a depth of 337.65 m, with another deformation sensor. Both deformation sensors measured the full strain tensor thanks to a Bragg optic fiber network, jointly with a fluid pressure sensor. A third borehole, located 2 m north of the monitoring probe, was dedicated to seismic monitoring. Two sets of collocated sensors, composed of a vertical geophone, a 3C accelerometer and an acoustic sensor, were positioned 9 m apart, above and below the main fault zone. These seismic sensors have a flat response in the ranges 0.01-0.5 kHz, 0.01-4 kHz and 0.5-10 kHz, respectively. Finally, the flowrate and pressure were also measured at the injection pump, located in the gallery.<br> For more details on the injection, we refer the reader to:<br> • Jeanne, P., Guglielmi, Y., Rutqvist, J., Nussbaum, C., Birkholzer, J., 2018. Permeability Variations Associated With Fault Reactivation in a Claystone Formation Investigated by Field Experiments and Numerical Simulations. J. Geophys. Res. Solid Earth 123, 1694–1710. https://doi.org/10.1002/2017JB015149<br> • Guglielmi, Y., Nussbaum, C., Cappa, F., De Barros, L., Rutqvist, J., Birkholzer, J., 2021. Field-scale fault reactivation experiments by fluid injection highlight aseismic leakage in caprock analogs: Implications for CO2 sequestration. Int. J. Greenh. Gas Control 111, 103471. https://doi.org/10.1016/j.ijggc.2021.103471<br> • Guglielmi, Y., Nussbaum, C., Jeanne, P., Rutqvist, J., Cappa, F., Birkholzer, J., 2020. Complexity of Fault Rupture and Fluid Leakage in Shale: Insights From a Controlled Fault Activation Experiment. J.Geophys. Res. Solid Earth 125, e2019JB017781. https://doi.org/10.1029/2019JB017781<br> • Guglielmi, Y., Cappa, F., Lançon, H., Janowczyk, J.B., Rutqvist, J., Tsang, C.F., Wang, J.S.Y., 2014. ISRM Suggested Method for Step-Rate Injection Method for Fracture In-Situ Properties (SIMFIP): Using a 3-Components Borehole Deformation Sensor. Rock Mech. Rock Eng. 47, 303–311. https://doi.org/10.1007/s00603-013-0517-1</p>
Figures 5-10 in Heleniella helvetica sp. n., a cold stenothermic species inhabiting the upper Rhône catchment in central Switzerland [Diptera, Chironomidae, Orthocladiinae]
Figures 5-10. Male imago of Heleniella spp. Heleniella helvetica sp. n.: hypopygium, dorsal (5) and ventral (6); anal point in lateral view (7); anal point and gonocoxite in lateral view (8). H. extrema:anal point and inferior volsella, dorsal, after Albu (1972, Figure 2) (9); gonocoxite with sternapodeme, phallapodeme and right gonostylus, ventral, after Albu (1972, Figure 2) (10).
Figures 1-4 in Heleniella helvetica sp. n., a cold stenothermic species inhabiting the upper Rhône catchment in central Switzerland [Diptera, Chironomidae, Orthocladiinae]
Figures 1-4. Male imago of Heleniella spp. Heleniella helvetica sp. n.: head, temporals (1); humeral pit with prealars and some episternals (2); thorax (3). H. extrema,thorax with dorsocentrals and scutellars, after Albu (1972, Figure 1) (4).
Figures 11-22 in Heleniella helvetica sp. n., a cold stenothermic species inhabiting the upper Rhône catchment in central Switzerland [Diptera, Chironomidae, Orthocladiinae]
Figures 11-22. Male imago of Heleniella spp. Heleniella helvetica sp. n.: anal point and distribution pattern of setae on tergite IX (11); virga (12); right gonostylus, dorsal (13); left gonostylus, ventral (14); inferior volsella and gonostylus, dorsal (15). H. sp. 1(central Switzerland): tergite IX lacking anal point (16); virga, two aspects (17-18); phallapodeme (19); right gonostylus (20). H. extrema:p hallapodeme, after Albu (1972, Figure 2) (21); left gonostylus, dorsal, after Albu (1972, Figure 2) (22).
Fig. 1 in On the Auguste Forel ant collection in the Naturmuseum Solothurn, Switzerland: current state and illustrated type catalogue (Hymenoptera, Formicidae)
Fig. 1. Syntypes ☿ dorsal/lateral views. (A) Strongylognathus huberi Forel, 1874. (B) Myrmica smythiesii Forel, 1902. (C) Monomorium indicum Forel, 1902. (D) Messor lobicornis Forel, 1894. (E) Camponotus bugnioni Forel, 1899. (F) Monomorium smithii Forel, 1892. (G) Temnothorax algiricus trabutii (Forel, 1894). Scale bars 1 mm.
Fig. 4 in On the Auguste Forel ant collection in the Naturmuseum Solothurn, Switzerland: current state and illustrated type catalogue (Hymenoptera, Formicidae)
Fig. 4. Original labels of 16 syntypes and 2 paralectotypes. (A) Strongylognathus huberi Forel, 1874. (B) Myrmica smythiesii Forel, 1902. (C) Monomorium indicum Forel, 1902. (D) Messor lobicornis Forel, 1894. (E) Camponotus bugnioni Forel, 1899. (F) Monomorium smithii Forel, 1892. (G) Temnothorax algiricus trabutii (Forel, 1894). (H) Temnothorax delaparti (Forel, 1890). (I) T. oraniensis (Forel, 1894). (J) Cardiocondyla stambuloffii Forel, 1892. (K) Solenopsis latro Forel, 1894. (L) Crematogaster ranavalonae Forel, 1887. (M) C. daisyi Forel, 1901. (N) Pogonomyrmex mayri Forel, 1899. (O) Azteca velox Forel, 1899. (P) A. delpini antillana Forel, 1899. (Q) Lasius myops Forel, 1894. (R) Cataglyphis savignyi (Dufour, 1862). (S) Camponotus alii Forel, 1890.
Fig. 3 in On the Auguste Forel ant collection in the Naturmuseum Solothurn, Switzerland: current state and illustrated type catalogue (Hymenoptera, Formicidae)
Fig. 3. (A) Paralectotype ☿ dorsal/lateral of Pogonomyrmex mayri Forel, 1899. (B) ☿ dorsal/lateral of Azteca velox Forel, 1899. (C) Syntypes ☿ of A. delpini antillana Forel, 1899. (D) Lasius myops Forel, 1894. (E) Cataglyphis savignyi (Dufour, 1862). (F) Camponotus alii Forel, 1890. Scale bars 1 mm.
Fig. 2 in On the Auguste Forel ant collection in the Naturmuseum Solothurn, Switzerland: current state and illustrated type catalogue (Hymenoptera, Formicidae)
Fig. 2. Syntypes ☿ dorsal/lateral views. (A) Temnothorax delaparti (Forel, 1890). (B) T. oraniensis (Forel, 1894). (C) Cardiocondyla stambuloffii Forel, 1892. (D) Solenopsis latro Forel, 1894. (E) Crematogaster ranavalonae Forel, 1887. (F) Paralectotype of C. daisyi Forel, 1901. Scale bars 1 mm.
Fig. 1 in Distribution and habitat requirements of red wood ants in Switzerland: Implications for conservation
Fig. 1. Distribution of mounds of red wood ants (Formica rufa group) in Switzerland, based on a systematic survey of forest plots. Each triangle denotes a plot in which one or more mounds were recorded. a) All F. rufa group species. b) F. lugubris. c) F. paralugubris. d) F. aquilonia. e) F. rufa. f) F. polyctena. Solid line: border between Swiss Plateau and Alps. Dashed line: border between Jura Mountains and Swiss Plateau.
Figure 4 in Heterochronic evolution explains novel body shape in a Triassic coelacanth from Switzerland
Figure 4. Reconstruction of the living coelacanth Foreyia maxkuhni gen. et sp. nov. Artwork by Alain Bénéteau.
Figure 3 in Heterochronic evolution explains novel body shape in a Triassic coelacanth from Switzerland
Figure 3. Phylogenetic relationships of Foreyia maxkuhni gen. et sp. nov. and developmental origin of the derived characters. (A) Strict consensus trees of the 259 most parsimonious trees of 317 steps (CI = 0.3817, RI = 0.6766) with some of the uniquely derived characters present in Foreyia maxkuhni on the left, and reconstructions of genera with atypical general morphology. (B and C) Shared features of Ticinepomis peyeri and Foreyia maxkuhni (in orange) not included in the cladistics analysis (see main text for numbers). (D) Reconstruction of a coelacanth embryo with localization of embryonic tissues that give rise the derived skeletal features present in Foreyia. It is hypothesized that changes in the expression of Pax 9 may have altered the derived characters shown in blue on the reconstruction (E). All the drawings were made by LC. Abbreviation: Boc, basioccipital; Cla, clavicle; Exo, exoccipital; lat. Meso., lateral mesoderm; neur. cr., neural crest; pect. f., pectoral fin; S (numbered), somite.
Figure 1 in Heterochronic evolution explains novel body shape in a Triassic coelacanth from Switzerland
Figure 1. Skeleton of the new coelacanth Foreyia maxkuhni gen. et sp. nov. (A) Photo and (B) outline of the holotype (PIMUZ A / I 4620). (C) Reconstruction of the whole skeleton.
Figure 2 in Heterochronic evolution explains novel body shape in a Triassic coelacanth from Switzerland
Figure 2. Osteological details of the new coelacanth Foreyia maxkuhni gen. et sp. nov. (A) Photo and (B) surface CT reconstruction of the skull of the paratype (PIMUZ A / I 4372). (C) Tubercles and denticles in the Holotype (PIMUZ A / I 4620) and (D) in the paratype (PIMUZ A / I 4372). 1, tubercles on the skull roof. 2, large spine-like tubercles on the posterior margin of the otico-occipital shield. 3, denticles on the fin rays of the first dorsal fin. 4, scales with denticles from the ventral margin of the caudal peduncle. 5, scales with denticles from the anal region. 6, scales with denticles from the belly region. 7, toothed coronoid bones. 8, scales with denticles from the flank. 9, supplementary caudal fin lobe with spiny scales. 10, Scales with denticles from the lobe of the anal fin.
Figure 2 in Phylogeography of the common toad (Bufo bufo, Lissamphibia: Anura) in Switzerland
Figure 2. Median-joining network of the mitochondrial 16 S rRNA gene in the B. bufo complex and outgroups. Black dots represent single substitution steps. Each haplotype is represented by a circle, with width proportional to frequency. Haplotypes represented by more than three specimens are labelled with a letter (A-M), the legend below the figure lists the associated specimens. The numbers correspond to the specimens listed in Appendix. Specimens from Switzerland in grey.
Figure 1 in Phylogeography of the common toad (Bufo bufo, Lissamphibia: Anura) in Switzerland
Figure 1. Map of Switzerland including localities of collected samples of Bufo bufo and the distribution of the corresponding mitochondrial haplotypes 1 and 2, which correspond to the haplotypes e 3 and e 1 of Garcia-Porta et al. (2012).
FIGURE 3 in Catalogue of the type specimens of Ichneumonidae (Hymenoptera) in the Jacques F. Aubert collection at the Musée de Zoologie, Lausanne, Switzerland
FIGURE 3. Labels of all specimens of the type series of Glypta suturalis italicator Aubert. In the original publication of this taxon, no holotype is designated. Both the original labels by Aubert and the syntype labels added by us are shown. (a) labels of the two individuals (one female and one male) marked as "Type" by Aubert. (b) labels of the three individuals marked as "Paratype".
FIGURE 2 in Catalogue of the type specimens of Ichneumonidae (Hymenoptera) in the Jacques F. Aubert collection at the Musée de Zoologie, Lausanne, Switzerland
FIGURE 2. Mounting and labeling by Aubert shown for (A) syntypes 1 and 2 of Lissonota bivittata gallicator Aubert, (B) Hybophanes ops meridionator Aubert, and (C) syntype 1 of Exetastes curvator Aubert.
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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.
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.