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zenodo32/100

Abb. 3 in Zwei für die Schweiz «neue» Florfliegenarten (Neuroptera: Chrysopidae) Two «new» lacewing species (Neuroptera: Chrysopidae) in Switzerland

Abb. 3. Lebensraum von Chrysopa walkeri bei San Antonio, Meride TI, 15. Mai 2005. Die Florfliegen fressen Blattläuse in der Krautschicht (Foto C. Monnerat).

opennotspecifiedDec 2016View details →
zenodo32/100

Fig. 2 in First records of Edwardsiana sociabilis (Ossiannilsson, 1936) and Laburrus pellax (Horváth, 1903) (Hemiptera, Auchenorrhyncha: Cicadellidae) in Switzerland

Fig. 2. Geographic locations of the gardens in the city of Zurich where the leafhopper species new to Switzerland were sampled with bowl and pitfall traps during the BetterGardens invertebrate survey between May 18th and August 19th 2015. Each individual reported in the text is assigned to its respective sampling site.

opennotspecifiedDec 2016View details →
zenodo32/100

FIGURE 11 in The Linsenmaier Chrysididae collection housed in the Natur-Museum Luzern (Switzerland) and the main results of the related GBIF Hymenoptera Project (Insecta)

FIGURE 11. Chrysis (Pentachrysis) zharptitza Semenov-Tian-Shanskij. Image taken from the manuscripts.

opennotspecifiedDec 2015View details →
zenodo32/100

FIGURE 16 in The Linsenmaier Chrysididae collection housed in the Natur-Museum Luzern (Switzerland) and the main results of the related GBIF Hymenoptera Project (Insecta)

FIGURE 16. Handwritten locality labels by Linsenmaier: A) original label handwritten in 1949; B) label probably rewritten in the 1980s.

opennotspecifiedDec 2015View details →
zenodo32/100

FIGURE 17 in The Linsenmaier Chrysididae collection housed in the Natur-Museum Luzern (Switzerland) and the main results of the related GBIF Hymenoptera Project (Insecta)

FIGURE 17. Type labels handwritten by Linsenmaier, based on specimens described in 1951: A) original label handwritten in 1951 (C. ignita var. mediata Linsenmaier, 1951); B) label rewritten probably in 1959 (H. amoenula var. virideaurata Linsenmaier, 1951); C) label rewritten in 1959 (original combination C. germari var. lucida Linsenmaier, 1951).

opennotspecifiedDec 2015View details →
zenodo32/100

Figs 1-6 in Lonchoptera vaillanti sp. nov., a new fly from Switzerland (Diptera: Lonchopteridae)

Figs 1-6. Lonchoptera vaillanti sp. nov., male. 2. male genitalia, dorsal view - 3. same, ventral view - 4. same, detail, scale is same as for fig 1. —5. left anterior gonapophysis - 6. apex of left posterior gonapophysis - 1. ventral view of segments 2-5 of right fore tarsus. Figs 5 and 6 are not to scale. aG, anterior gonapophysis; C, cercus; P proctiger; pG, posterior gonapophysis; S9, sternite IX; T9, tergite IX.

opennotspecifiedDec 2004View details →
zenodo32/100

Figs 1-9. Glanitaenia osculata from Silurus glanis, Switzerland. 1-7 in An emendation of the generic diagnosis of the monotypic Glanitaenia (Cestoda: Proteocephalidae), with notes on the geographical distribution of G. osculata, a parasite of invasive wels catfish

Figs 1-9. Glanitaenia osculata from Silurus glanis, Switzerland. 1-7. Scanning electron micrographs (INVE-PLAT-91260). (1) Scolex, dorsoventral view. (2) Scolex, apical view. (3) Scolex, lateral view. (4) Acicular filitriches on the apex of the scolex. (5) Papilliform filitriches on the internal surface of suckers. (6) Capilliform filitriches between the suckers. (7) Gladiate spinitriches on the external surface of the proliferation zone (neck). (8, 9.) Photomicrographs of longitudinal sections of the scolex (INVE-PLAT-91260). (8) Detail of the apical part of the scolex showing an apical sucker. (9) Detail of the dense network of osmoregulatory canals in the posterior part of the scolex and the anterior part of the neck (proliferation zone).

opennotspecifiedDec 2016View details →
zenodo32/100

Switzerland Synthetic Ecosystem

Switzerland synthetic ecosystem dataset consisting of tables for persons and households. This dataset was created by the SPEW R Package using the following input data sources: GeoHive counts and IPUMS-I shapefiles and microdata.

opencc-by-4.0May 2017View details →
zenodo32/100

Concentrated Hybrid Solar Panel Real Measurements in Switzerland

<h3>Measurements of concentrated hybrid solar panel</h3> <p>Datasheet of the hybrid PV panel (<a title="Datasheet" href="https://cdn.enfsolar.com/Product/pdf/Crystalline/55adc587c2506.pdf" target="_blank" rel="noopener">Here</a>)</p> <p>These measurements have taken place in Granges, Valais, Switzerland in longitude: 7.4649965&deg; and latitude: 46.2647793&deg; with three flat mirrors that concentrated the sun's reflection on one hybrid panel.</p> <p>The PV-T and each mirror length (L) : 1 m</p> <p>The distance between the mirrors (D) : 1.5 m</p> <p>The distance between the mirrors and PV-T (F) : 10 m</p>

opencc-by-4.0Aug 2024View details →
zenodo32/100

Raw geolocator data of Hoopes Upupa epops from Switzerland

<p>Raw multi-sensor geolocator data of&nbsp;Hoopes breeding in Wallis, Switzerland</p>

opencc-by-4.0Mar 2024View details →
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Subspecies and Distribution. N. p. procyonoides Gray, 1834 — W & SW China and N Indochina. N. p. albus Hornaday, 1904 — Japan (Hokkaido). N. p. koreensis Mori, 1922 — Korean Peninsula. N. p. orestes Thomas, 1923 — C & S China. N. p. ussuriensis Matschie, 1907 — NE China, E Mongolia, and SE Russia. N. p. viverrinus Temminck, 1839 — Japan. Introduced (ussuriensis) to the Baltic states, Belarus, Bulgaria, Czech Republic, Finland, Germany, Hungary, Moldova, Poland, Romania, W Russia, Serbia, Slovakia, Sweden, and Ukraine, occasionally seen in Austria, Bosnia, Denmark, France, the Netherlands, Norway, Slovenia, and Switzerland. in Canidae

Subspecies and Distribution. N. p. procyonoides Gray, 1834 — W &amp; SW China and N Indochina. N. p. albus Hornaday, 1904 — Japan (Hokkaido). N. p. koreensis Mori, 1922 — Korean Peninsula. N. p. orestes Thomas, 1923 — C &amp; S China. N. p. ussuriensis Matschie, 1907 — NE China, E Mongolia, and SE Russia. N. p. viverrinus Temminck, 1839 — Japan. Introduced (ussuriensis) to the Baltic states, Belarus, Bulgaria, Czech Republic, Finland, Germany, Hungary, Moldova, Poland, Romania, W Russia, Serbia, Slovakia, Sweden, and Ukraine, occasionally seen in Austria, Bosnia, Denmark, France, the Netherlands, Norway, Slovenia, and Switzerland.

opennotspecifiedJan 2009View details →
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Subspecies and Distribution. M. e. erminea Linnaeus, 1758 — Finland, Norway, NW Russia, and Sweden. M. e. aestiva Kerr, 1792 — most of mainland N & C Europe to C Asia in Kazakhstan, Kyrgyzstan, and Tajikistan. M. e. alascensis Merriam, 1896 — S Alaska. M. e. anguinae Hall, 1932 — SW Canada (Vancouver I, British Columbia). M. e. arctica Merriam, 1896 — Alaska and NW Canada. M. e. bangsi Hall, 1945 — C Canada and NC USA. M. e. celenda Hall, 1944 — Alaska (Prince of Wales I). M.e. cicognanii Bonaparte, 1838 — SE Canada and NE USA. M. e. fallenda Hall, 1945 — W Canada (British Columbia) and NW USA (N Washington). M. e. ferghanae Thomas, 1895 — Afghanistan, N India, and Pakistan. M.e. gulosa Hall, 1945 — NW USA (E Washington). M.e. haidarum Preble, 1898 — W Canada (Queen Charlotte Is, British Columbia). M.e. hibernica Thomas & Barrett-Hamilton, 1895 — Ireland. M.e. imatis Hall, 1944 — Alaska (Baranof I). M.e. invicta Hall, 1945 — SW Canada (Alberta) and NW USA (Idaho & Montana). M.e. kadiacensis Merriam, 1896 — Alaska (Kodiak I). M.e. kaneti Baird, 1857 — NE China, Russia (E Siberia). M.e. karaginensis Jurgenson, 1936 — NE Russia (Karaginsky I). M.e. lymani Hollister, 1912 — E Russia (Altai Mts, Siberia). M.e. minima Cavazza, 1912 — Switzerland. M.e. mongolica Ognev, 1928 — NW China and Mongolian Altai. M. e. muricus Bangs, 1899 — USA (N California, Colorado, Idaho, New Mexico, Nevada, Oregon, South Dakota, Utah & Wyoming). M. e. nippon Cabrera, 1913 — Japan. M.e. olympica Hall, 1945 — NW USA (Olympic Peninsula, Washington). M.e. polaris Barrett-Hamilton, 1904 — Greenland. M.e.richardsonii Bonaparte, 1838 — N Canada. M.e. ricinae G. S. Miller, 1907 — Scotland (Islay I). M.e.salva Hall, 1944 — SE Alaska (Admiralty I). M.e.seclusa Hall, 1944 — SE Alaska (Suemez I). M.e.sempler Sutton & Hamilton, 1932 — Canada (Franklin & Keewatin Districts). M.e.stabilis Barrett-Hamilton, 1904 — Great Britain. M.e.streatori Merriam, 1896 — W USA (NE California, Oregon & coastal Washington). M.e.teberdina Kornejv, 1941 — Russian Caucasus. M.e. tobolica Ognev, 1923 — W Siberia. Introduced to New Zealand. in Mustelidae

Subspecies and Distribution. M. e. erminea Linnaeus, 1758 — Finland, Norway, NW Russia, and Sweden. M. e. aestiva Kerr, 1792 — most of mainland N &amp; C Europe to C Asia in Kazakhstan, Kyrgyzstan, and Tajikistan. M. e. alascensis Merriam, 1896 — S Alaska. M. e. anguinae Hall, 1932 — SW Canada (Vancouver I, British Columbia). M. e. arctica Merriam, 1896 — Alaska and NW Canada. M. e. bangsi Hall, 1945 — C Canada and NC USA. M. e. celenda Hall, 1944 — Alaska (Prince of Wales I). M.e. cicognanii Bonaparte, 1838 — SE Canada and NE USA. M. e. fallenda Hall, 1945 — W Canada (British Columbia) and NW USA (N Washington). M. e. ferghanae Thomas, 1895 — Afghanistan, N India, and Pakistan. M.e. gulosa Hall, 1945 — NW USA (E Washington). M.e. haidarum Preble, 1898 — W Canada (Queen Charlotte Is, British Columbia). M.e. hibernica Thomas &amp; Barrett-Hamilton, 1895 — Ireland. M.e. imatis Hall, 1944 — Alaska (Baranof I). M.e. invicta Hall, 1945 — SW Canada (Alberta) and NW USA (Idaho &amp; Montana). M.e. kadiacensis Merriam, 1896 — Alaska (Kodiak I). M.e. kaneti Baird, 1857 — NE China, Russia (E Siberia). M.e. karaginensis Jurgenson, 1936 — NE Russia (Karaginsky I). M.e. lymani Hollister, 1912 — E Russia (Altai Mts, Siberia). M.e. minima Cavazza, 1912 — Switzerland. M.e. mongolica Ognev, 1928 — NW China and Mongolian Altai. M. e. muricus Bangs, 1899 — USA (N California, Colorado, Idaho, New Mexico, Nevada, Oregon, South Dakota, Utah &amp; Wyoming). M. e. nippon Cabrera, 1913 — Japan. M.e. olympica Hall, 1945 — NW USA (Olympic Peninsula, Washington). M.e. polaris Barrett-Hamilton, 1904 — Greenland. M.e.richardsonii Bonaparte, 1838 — N Canada. M.e. ricinae G. S. Miller, 1907 — Scotland (Islay I). M.e.salva Hall, 1944 — SE Alaska (Admiralty I). M.e.seclusa Hall, 1944 — SE Alaska (Suemez I). M.e.sempler Sutton &amp; Hamilton, 1932 — Canada (Franklin &amp; Keewatin Districts). M.e.stabilis Barrett-Hamilton, 1904 — Great Britain. M.e.streatori Merriam, 1896 — W USA (NE California, Oregon &amp; coastal Washington). M.e.teberdina Kornejv, 1941 — Russian Caucasus. M.e. tobolica Ognev, 1923 — W Siberia. Introduced to New Zealand.

opennotspecifiedJan 2009View details →
zenodo32/100

Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae

Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C &amp; S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W &amp; SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux &amp; Festa, 1927 — C &amp; S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S &amp; E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.

opennotspecifiedAug 2011View details →
zenodo32/100

Fig. 35 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)

Fig. 35: View from about 2100 m a. s. l. to Corn dal Solcun. Dichotrachelus sondereggeri sp. nov. was found in a single exemplar collected by C. Besuchet at this lower altitude. Foto: C. Germann.

opennotspecifiedMay 2011View details →
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Figs 33–34 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)

Figs 33–34. Biotope of Dichotrachelus sondereggeri sp. nov. on Corn dal Solcun (2480 m a.s.l.): 33) side peak in loose rocks providing a cold and humid microclimate where moss cushions with larvae were found; 34) detailed view of those moss cushions. Fotos: C. Germann.

opennotspecifiedMay 2011View details →
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Figs 29–32 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)

Figs 29–32: Different stages of Dichotrachelus sondereggeri sp. nov.: 29) last instar larva just before pupation; 30) pupa ventral view; 31) pupa dorsal view; 32) freshly hatched imago. Fotos: C. Germann.

opennotspecifiedMay 2011View details →
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Fig. 27 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)

Fig. 27: Map showing sites of Dichotrachelus alpestris species group. Black circles: D. alpestris; black square: D. sondereggeri sp. nov.; white squares: D. augusti species complex.

opennotspecifiedMay 2011View details →
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Figs 8–10 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)

Figs 8–10: Dorsal and lateral views: 8) Dichotrachelus alpestris from Monte Viso, male; 9) Ditto from Anzeindaz, female; 10) Ditto male.

opennotspecifiedMay 2011View details →
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Figs 11–16 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)

Figs 11–16: Overview of the variability of the tip of the aedeagus of Dichotrachelus alpestris: 11) Waadt, Anzeindaz; 12) Ticino, Monte Gene-Generoso; 13) Valle Aosta, Colle Arietta; 14) Valle Aosta, Champorcher; 15) Piemonte, Colle della Lombarda; 16) Piemonte, Portette Valdieri.

opennotspecifiedMay 2011View details →
zenodo32/100

Figs 2–4 in Review of the Dichotrachelus alpestris STIERLIN, 1878 species group with evidence for a species complex of D. augusti F. SOLARI, 1946, and D. sondereggeri sp. nov. from Switzerland (Coleoptera, Curculionidae)

Figs 2–4: Dorsal and lateral views: 2) Dichotrachelus sondereggeri sp. nov. from Corn dal Solcun, male; 3) Ditto female; 4) Ditto male.

opennotspecifiedMay 2011View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record