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FIGURE 3 in Draeculacephala robinsoni Hamilton, 1967 (Hemiptera: Auchenorrhyncha Cicadellidae), a newly introduced species and genus in Europe with comments on its identification
FIGURE 3. Living specimens of Draeculacephala robinsoni in the field in the Aiguamolls de l'Empordà (Castelló d'Empuries), Catalonia, Spain. A) A male and two females, 26.viii.2021, B) Female, 04.ix.2021, C) Nymph, 04.ix.2021. Pictures taken by EM (A) and AMN (B+C).
FIGURE 1 in Draeculacephala robinsoni Hamilton, 1967 (Hemiptera: Auchenorrhyncha Cicadellidae), a newly introduced species and genus in Europe with comments on its identification
FIGURE 1. Map showing the sampling locations in France (Pyrenées-Orientales) and Spain (Catalonia) in 2021. Closed circles: presence of Draeculacephala robinsoni, open circles: D. robinsoni was not found. For exact coordinates see Table 1.
Subspecies and Distribution. A.l.lerviaPallas,1777—Morocco,NA.l.,andNTunisia. A.l.angusiRothschild,1921—NWNiger(Air&TermitMassifs). A.l.blaineiRothschild,1913—SELybia,NEChad,andNW&NESudan(probablynowrestrictedtoRedSeahills). A.l.fassiniLepri,1930—NWLibya,extremeSTunisia. A.l.ornatus1.GeoffroySaint-Hilaire,1827—SE&SWEgypt. A. l. sahariensis Rothschild, 1913 — S Morocco, Western Sahara, NW Mauritania, S A.l ria, extreme S Libya, NE Mali, SE Niger, and NW Chad. Introduced, free-ranging populations occur in S Spain, the Canary Is, USA (California, New Mexico, and Texas), and NE Mexico. Subspecies of free-ranging introduced populations are unknown because they originate from zoo animals of uncertain origin or from hybrids. Most introduced populations are probably from subspecies lervia, derived from European zoos. The Aoudad has become a widespread invasive species. in Bovidae
Subspecies and Distribution. A.l.lerviaPallas,1777—Morocco,NA.l.,andNTunisia. A.l.angusiRothschild,1921—NWNiger(Air&TermitMassifs). A.l.blaineiRothschild,1913—SELybia,NEChad,andNW&NESudan(probablynowrestrictedtoRedSeahills). A.l.fassiniLepri,1930—NWLibya,extremeSTunisia. A.l.ornatus1.GeoffroySaint-Hilaire,1827—SE&SWEgypt. A. l. sahariensis Rothschild, 1913 — S Morocco, Western Sahara, NW Mauritania, S A.l ria, extreme S Libya, NE Mali, SE Niger, and NW Chad. Introduced, free-ranging populations occur in S Spain, the Canary Is, USA (California, New Mexico, and Texas), and NE Mexico. Subspecies of free-ranging introduced populations are unknown because they originate from zoo animals of uncertain origin or from hybrids. Most introduced populations are probably from subspecies lervia, derived from European zoos. The Aoudad has become a widespread invasive species.
Subspecies and Distribution. R.m.mariannaDesmarest,1822—Luzon|andassociatedsmallerIs. R.m.barandanaHeude,1888—MindoroI. R. m. nigella Hollister, 1813 — Mindanao, Basilan, Samar, and Leyte Is. In addition to its native range, introduced populations of this species are found on the islands of Guam, Saipan and Rota in the Mariana Is and Pohnpei in the Caroline Is. The Philippine Brown Deer was also introduced to the Japanese Bonin Islands, where it later became extinct. in Cervidae
Subspecies and Distribution. R.m.mariannaDesmarest,1822—Luzon|andassociatedsmallerIs. R.m.barandanaHeude,1888—MindoroI. R. m. nigella Hollister, 1813 — Mindanao, Basilan, Samar, and Leyte Is. In addition to its native range, introduced populations of this species are found on the islands of Guam, Saipan and Rota in the Mariana Is and Pohnpei in the Caroline Is. The Philippine Brown Deer was also introduced to the Japanese Bonin Islands, where it later became extinct.
FIGURES 35–42. Female genitalia. 35 in Taxonomic review of the genus Morabia Hausmann & Tujuba, 2020 with descriptions of two new species and introducing five new generic combinations (Lepidoptera, Geometridae, Ennominae)
FIGURES 35–42. Female genitalia. 35, Morabia politzari, RSA, gen. slide No.: NHMUK 010317360 (NHMUK); 36, M. nigripunctata, Sierra Leone, gen. slide No.: NHMUK 010317229 (NHMUK); 37, Ibidem, Zambia, gen. slide No.: NHMUK 010317362 (NHMUK); 38, M. cryptica sp. n., PT, gen. slide No.: NHMUK 010317361 (NHMUK); 39, M. distinctaria, Mauritius, gen. slide No.: NHMUK 010317355 (NHMUK); 40, M. hero, Madagascar, gen. slide No.: NHMUK 010317356 (NHMUK); 41, M. herbuloti, Reunion, gen. slide No.: G 21274 (ZSM); 42, M. pluto, Madagascar, gen. slide No.: NHMUK 010317354 (NHMUK).
FIGURES 1–10. Adults, a in Taxonomic review of the genus Morabia Hausmann & Tujuba, 2020 with descriptions of two new species and introducing five new generic combinations (Lepidoptera, Geometridae, Ennominae)
FIGURES 1–10. Adults, a: dorsal, b: ventral view. 1, Morabia politzari, ♂, RSA (RCHS); 2, Ibidem, ♀, RSA (NHMUK); 3, M. nigripunctata, ST, ♂, Nigeria (NHMUK); 4, Ibidem, ♀, Sierra Leone (NHMUK); 5, Ibidem, ♂, Mozambique (ANHRT); 6, Ibidem, ♀, Malawi (NHMUK); 7, M. cryptica sp. n., HT, ♂, Zambia (ANHRT); 8, Ibidem, PT, ♂, Zambia (ANHRT); 9, Ibidem, PT, ♀, Zambia (RCAK); 10, M. brunnea, ♂, Zambia (ANHRT).
FIGURES 20–28. Male genitalia, a in Taxonomic review of the genus Morabia Hausmann & Tujuba, 2020 with descriptions of two new species and introducing five new generic combinations (Lepidoptera, Geometridae, Ennominae)
FIGURES 20–28. Male genitalia, a: clasping apparatus, b: aedeagus. 20, Morabia politzari, Mozambique, slide No. LG 5467 (ANHRT); 21, Ibidem, RSA, slide No. LG 5528 (RCHS); 22, M. nigripunctata, HT, Nigeria, slide No. BM Geo 4990 (NHMUK); 23, Ibidem, Sierra Leone, slide No. LG 5520 (ANHRT); 24, Ibidem, Gabon, slide No. G 21276 (ZSM); 25, Ibidem, Mozambique, slide No. LG 5288 (ANHRT); 26, M. cryptica sp. n., HT, Zambia, slide No. LG 5289 (ANHRT); 27, Ibidem, PT, DRC, slide No. NHMUK 010317364 (NHMUK); 28, M. brunnea, Zambia, slide No. LG 5300 (ANHRT).
FIGURES 29–34. Male genitalia, a in Taxonomic review of the genus Morabia Hausmann & Tujuba, 2020 with descriptions of two new species and introducing five new generic combinations (Lepidoptera, Geometridae, Ennominae)
FIGURES 29–34. Male genitalia, a: clasping apparatus, b: aedeagus. 29, Morabia brunnea, Zambia, slide No. LG 5287 (ANHRT); 30, M. smithi sp. n., HT, Zambia, slide No. LG 5301 (ANHRT); 31, Ibidem, PT, Zambia, slide No. LG 5329 (ANHRT); 32, M. distinctaria, Mauritius, slide No. LG 5521 (ANHRT); 33, M. hero, Madagascar, slide No. G 21271 (ZSM); 34, M. pluto, Madagascar, slide No. NHMUK 010317353 (NHMUK).
FIGURES 11–19. Adults, a in Taxonomic review of the genus Morabia Hausmann & Tujuba, 2020 with descriptions of two new species and introducing five new generic combinations (Lepidoptera, Geometridae, Ennominae)
FIGURES 11–19. Adults, a: dorsal, b: ventral view. 11, Morabia smithi sp. n., HT, ♂, Zambia (ANHRT); 12, Ibidem, PT, ♂, Zambia (ANHRT); 13, M. distinctaria, ♂, Mauritius (ANHRT); 14, Ibidem, ♀, Mauritius (ANHRT); 15, M. hero, ♂, Madagascar (ZSM); 16, Ibidem, ♀, Madagascar (NHMUK); 17, M. herbuloti, ♀, Reunion (ZSM); 18, M. pluto, ♂, Madagascar (ZSM); 19, Ibidem, ♀, Madagascar (ZSM).
Subspecies and Distribution. L.n.nigricollisF.Cuvier,1823—SIndia(SoftheGodavariRiver). L.n.aryabertensisHodgson,1844—SCNepal. L.n.dayanusBlanford,1874—SEPakistanandNWIndia(GreatIndianDesert). L.n.ruficaudatusE.GeoffroySaint-Hilaire,1826—EPakistan,NIndia,SNepal,Bangladesh,Bhutan,exceptthehigherreachesoftheHimalayasandthemangroveareaswithintheSundarbans. L.n.sadiyaKloss,1918—NEIndia(Assam). L.n.simcoxiWroughton,1912—CIndia(NMaharashtraandMadhyaPradesh). L. n. singhala Wroughton, 1915 — Sri Lanka. Indian hares (probably ruficaudatus) also occur in extreme E Afghanistan, in the border areas with Pakistan. Situation in Java is debated and the so called "Javan Hare" might be native there. The species has been introduced by founder individuals of either unknown subspeciesaffiliation or belonging to various subspecies into Comoro, Mayotte, Madagascar, Réunion (including Gunners Quoin I), Mauritius (Agaléga Is), Seychelles (Cousin I), and Andaman Is in the Indian Ocean, and into New Guinea. In Gunners Quoin the Indian Hare has been eradicated. in Leporidae
Subspecies and Distribution. L.n.nigricollisF.Cuvier,1823—SIndia(SoftheGodavariRiver). L.n.aryabertensisHodgson,1844—SCNepal. L.n.dayanusBlanford,1874—SEPakistanandNWIndia(GreatIndianDesert). L.n.ruficaudatusE.GeoffroySaint-Hilaire,1826—EPakistan,NIndia,SNepal,Bangladesh,Bhutan,exceptthehigherreachesoftheHimalayasandthemangroveareaswithintheSundarbans. L.n.sadiyaKloss,1918—NEIndia(Assam). L.n.simcoxiWroughton,1912—CIndia(NMaharashtraandMadhyaPradesh). L. n. singhala Wroughton, 1915 — Sri Lanka. Indian hares (probably ruficaudatus) also occur in extreme E Afghanistan, in the border areas with Pakistan. Situation in Java is debated and the so called "Javan Hare" might be native there. The species has been introduced by founder individuals of either unknown subspeciesaffiliation or belonging to various subspecies into Comoro, Mayotte, Madagascar, Réunion (including Gunners Quoin I), Mauritius (Agaléga Is), Seychelles (Cousin I), and Andaman Is in the Indian Ocean, and into New Guinea. In Gunners Quoin the Indian Hare has been eradicated.
Distribution. New Guinea, including Yapen, Mios Num, and Roon Is in Cenderawasih (= Geelvink) Bay, Karkar and Walis Is off the N coast, Raja Ampat Is of Salawati, Sorong, and Misool, SE Papua New Guinea Is of Samarai (= Dinner) and Dufaure (= Dufour), and Aru Is. It is present on many islands of C & S Moluccas (Seram, Ambon, Pulau Pandjang, Buru, and the Tayandu and Kai archipelagos). It has been introduced to Selayar I between Sulawesi and Flores (W occurrence of the species), and there are vague records from Flores and Sulawesi, which may also refer to the Selayar population. This species was also apparently introduced to Mussau (St. Matthias Group, NE Bismarck Archipelago) in prehistoric times and to New Ireland I (Bismarck Archipelago) in the 20™ century. in Phalangeridae
Distribution. New Guinea, including Yapen, Mios Num, and Roon Is in Cenderawasih (= Geelvink) Bay, Karkar and Walis Is off the N coast, Raja Ampat Is of Salawati, Sorong, and Misool, SE Papua New Guinea Is of Samarai (= Dinner) and Dufaure (= Dufour), and Aru Is. It is present on many islands of C & S Moluccas (Seram, Ambon, Pulau Pandjang, Buru, and the Tayandu and Kai archipelagos). It has been introduced to Selayar I between Sulawesi and Flores (W occurrence of the species), and there are vague records from Flores and Sulawesi, which may also refer to the Selayar population. This species was also apparently introduced to Mussau (St. Matthias Group, NE Bismarck Archipelago) in prehistoric times and to New Ireland I (Bismarck Archipelago) in the 20™ century.
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa. in Molossidae
Distribution. Restricted to Réunion I; there is an isolated record from S Ethiopia, some several hundred kilometers from the coast. This record represents a vagrant or introduced individual, and the species does not normally occur in Africa.
Distribution. SE Ghana (E of Volta River), Togo, Benin, Nigeria, and NW Cameroon (to a little S of the Sanaga River). The species has been introduced to the Gulf of Guinea islands of Sao Tomé and Principe, and into the Caribbean islands of Grenada, Saint Kitts, and Nevis. in Cercopithecidae
Distribution. SE Ghana (E of Volta River), Togo, Benin, Nigeria, and NW Cameroon (to a little S of the Sanaga River). The species has been introduced to the Gulf of Guinea islands of Sao Tomé and Principe, and into the Caribbean islands of Grenada, Saint Kitts, and Nevis.
Distribution. India, the species' range extends 1900 km W to E, and includes all populations with the northern-type tail carriage between the Tapti River in Gujarat State and Krishna River in Andhra Pradesh State to the foothills of the Himalaya. Introduced into SW Bangladesh, where the population may have arisen from descendents of a pair introduced by Hindu pilgrims on the banks of the Jalangi River. in Cercopithecidae
Distribution. India, the species' range extends 1900 km W to E, and includes all populations with the northern-type tail carriage between the Tapti River in Gujarat State and Krishna River in Andhra Pradesh State to the foothills of the Himalaya. Introduced into SW Bangladesh, where the population may have arisen from descendents of a pair introduced by Hindu pilgrims on the banks of the Jalangi River.
FIGURES 6–10. Gyrodactylus breviradix n in Two new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea: Gyrodactylidae) parasitizing introduced poeciliids in Patagonia
FIGURES 6–10. Gyrodactylus breviradix n. sp. 6. Whole specimen. 7. Haptor. 8. Marginal hook. 9. Male copulatory organs. 10. Anchor.
FIGURES 11–12 in Two new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea: Gyrodactylidae) parasitizing introduced poeciliids in Patagonia
FIGURES 11–12. Comparison of marginal hook hooklets among the two new species from Patagonia Argentina (solid line) and the most similar neotropical Gyrodactylus especies (broken line). 11. Gyrodactylus decemmaculati n. sp. and the overlapping hooklets. 12. Gyrodactylus breviradix n. sp. and the overlapping hooklets.
FIGURE 13 in Two new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea: Gyrodactylidae) parasitizing introduced poeciliids in Patagonia
FIGURE 13. Maximum Likelihood method based on the Tamura-Nei model. The tree with the highest log likelihood (- 3376.1634) is shown and distances were estimated using the Maximum Composite Likelihood (MCL) approach, and then selecting the topology with superior log likelihood value. Branch lengths are measured as the number of substitutions per site. The analysis involved 25 nucleotide sequences.
FIGURE 14 in Two new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea: Gyrodactylidae) parasitizing introduced poeciliids in Patagonia
FIGURE 14. Blue line: Distribution of pairwise distance comparisons within species of gyrodactylids (without putative new ones) and between species (red line). Black dots represent de pairwise distance of newly proposed species (intraspecific), and green dots represent the pairwise comparisons of putative species with other gyrodactylids (interespecific).
FIGURES 1–5. Gyrodactylus decemmaculati n in Two new species of Gyrodactylus von Nordmann, 1832 (Monogenoidea: Gyrodactylidae) parasitizing introduced poeciliids in Patagonia
FIGURES 1–5. Gyrodactylus decemmaculati n. sp. 1. Whole specimen. 2. Haptor. 3. Marginal hook. 4. Male copulatory organs. 5. Anchor.
Figure 1 in The conservation paradox of an introduced population of a threatened species: spadefoot toads in the coastal dunes of the Netherlands
Figure 1. Sampling sites of the common spadefoot toad (Pelobates fuscus). The main map shows localities sampled outside and the inset localities sampled inside the Netherlands (see main text for details). A rough outline of the natural distribution range in the Netherlands is shaded grey. Localities that contain haplotypes found in the Netherlands are colour coded; otherwise they are left grey (FUS stands for P. fuscus). Sampling details are in supplementary table S1.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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