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Subspecies and Distribution. B.b.barbastellusSchreber,1774—EuropefromIrelandandIberianPeninsulaEtoLaivia,Belarus,Ukraine,andtheCauca-sus;alsomajorMediterraneanIs,Moroc-co,andTurkey(Anatolia);possiblyextinctinBelgium,Netherlands,andNorway. B. b. guanchae Trujillo, Ibanez & Juste, 2002 — Canary Is (Tenerife and La Gomera). in Vespertilionidae
Subspecies and Distribution. B.b.barbastellusSchreber,1774—EuropefromIrelandandIberianPeninsulaEtoLaivia,Belarus,Ukraine,andtheCauca-sus;alsomajorMediterraneanIs,Moroc-co,andTurkey(Anatolia);possiblyextinctinBelgium,Netherlands,andNorway. B. b. guanchae Trujillo, Ibanez & Juste, 2002 — Canary Is (Tenerife and La Gomera).
Subspecies and Distribution. M. m. megalophylla Peters, 1864 — from SW Arizona and Texas, USA, and Baja California, Mexico, S to W Nicaragua. M. m. carteriJ. D. Smith, 1972 — Carchi and Pichincha provinces, N Ecuador, and Lambayeque Department, NW Peru. M. m. intermedia G. S. Miller, 1900 — Netherlands Antilles (Aruba, Curacao, and Bonaire). M. m. tumidiceps G. S. Miller, 1902 — coastal and inland localities between C & E Andes ranges of Colombia, Caribbean coast of Venezuela including Margarita I, and Trinidad I. in Mormoopidae
Subspecies and Distribution. M. m. megalophylla Peters, 1864 — from SW Arizona and Texas, USA, and Baja California, Mexico, S to W Nicaragua. M. m. carteriJ. D. Smith, 1972 — Carchi and Pichincha provinces, N Ecuador, and Lambayeque Department, NW Peru. M. m. intermedia G. S. Miller, 1900 — Netherlands Antilles (Aruba, Curacao, and Bonaire). M. m. tumidiceps G. S. Miller, 1902 — coastal and inland localities between C & E Andes ranges of Colombia, Caribbean coast of Venezuela including Margarita I, and Trinidad I.
Distribution. Dry tropical areas of N & W Colombia, N & W Venezuela (including Margarita I), and Netherlands Antilles (Aruba, Curacao, and Bonaire Is). in Phyllostomidae
Distribution. Dry tropical areas of N & W Colombia, N & W Venezuela (including Margarita I), and Netherlands Antilles (Aruba, Curacao, and Bonaire Is).
Subspecies and Distribution. C. p. paca Linnaeus, 1766 — E & S Colombia, Venezuela, the Guianas, and E Brazil to Paraguay, N Argentina (Misiones and Corrientes provinces), and Uruguay. C. p. guanta Lonnberg, 1921 — W Brazil, Ecuador, Peru, and N Bolivia. C. p. mexianae Hagmann, 1908 — E Brazil, mouth of the Amazon in Para State. C. p. nelsoni Goldman, 1913 — E & S Mexico (Atlantic slope lowlands from San Luis Potosi State to Yucatan Peninsula), then through Central America to N Costa Rica. C. p. virgatus Bangs, 1902 — W Costa Rica, through Panama to N & W Colombia. It is also naturally present in Trinidad and Tobago Is (subspecies unknown), but it was extinct in Tobago I long ago due to overexploitation by Amerindians. They also introduced the Lowland Paca (nominate subspecies) from Venezuela into Curacao I, the largest of the Netherlands Antilles. In the 20" century it was successfully introduced into Cuba from Mexico, so it should belong to the Mexican subspecies nelson in Cuniculidae
Subspecies and Distribution. C. p. paca Linnaeus, 1766 — E & S Colombia, Venezuela, the Guianas, and E Brazil to Paraguay, N Argentina (Misiones and Corrientes provinces), and Uruguay. C. p. guanta Lonnberg, 1921 — W Brazil, Ecuador, Peru, and N Bolivia. C. p. mexianae Hagmann, 1908 — E Brazil, mouth of the Amazon in Para State. C. p. nelsoni Goldman, 1913 — E & S Mexico (Atlantic slope lowlands from San Luis Potosi State to Yucatan Peninsula), then through Central America to N Costa Rica. C. p. virgatus Bangs, 1902 — W Costa Rica, through Panama to N & W Colombia. It is also naturally present in Trinidad and Tobago Is (subspecies unknown), but it was extinct in Tobago I long ago due to overexploitation by Amerindians. They also introduced the Lowland Paca (nominate subspecies) from Venezuela into Curacao I, the largest of the Netherlands Antilles. In the 20" century it was successfully introduced into Cuba from Mexico, so it should belong to the Mexican subspecies nelson
FIGURE 1. a–c in New records of Encyrtidae (Hymenoptera: Chalcidoidea) from the Netherlands with a description of new species
FIGURE 1. a–c: Adelencyrtus aulacaspis, female. a, dorsal habitus; b, ventral habitus; c, lateral habitus. d–f: Blastothrix hungarica, female. d, dorsal habitus; e, ventral habitus; f, lateral habitus.
FIGURE 4. a–h in New records of Encyrtidae (Hymenoptera: Chalcidoidea) from the Netherlands with a description of new species
FIGURE 4. a–h: Microterys nederlandicus sp. n., female. a, dorsal habitus; b, ventral habitus; c, lateral habitus; d, antennae; e, mesosoma; f, mandible; g, wings; h, ovipositor.
FIGURE 7. a–c in New records of Encyrtidae (Hymenoptera: Chalcidoidea) from the Netherlands with a description of new species
FIGURE 7. a–c: Syrphophagus ariantes, female. a, dorsal habitus; b, lateral habitus; c, ventral habitus; d–f: S. arundinicola, female. d, dorsal habitus; e, lateral habitus; f, ventral habitus; g–i: S. herbidus, female. g, dorsal habitus; h, lateral habitus; i, ventral habitus; j–l S. taeniatus, female. j, dorsal habitus; k, lateral habitus; l, ventral habitus.
FIGURE 3. a–c in New records of Encyrtidae (Hymenoptera: Chalcidoidea) from the Netherlands with a description of new species
FIGURE 3. a–c: Lamennaisia nobilis, female. a, dorsal habitus; b, lateral habitus; c, ventral habitus; d–f: Metaphycus dispar, female. d, dorsal habitus; e, lateral habitus; f, ventral habitus; g–i: M. insidiosus, female. g, dorsal habitus; h, lateral habitus; i, ventral habitus.
FIGURE 2. a–c in New records of Encyrtidae (Hymenoptera: Chalcidoidea) from the Netherlands with a description of new species
FIGURE 2. a–c: Bothriothorax intermedius, female. a, dorsal habitus; b, ventral habitus; c, lateral haabitus; d–f: Ixodiphagus hookeri, female. d, lateral habitus; e, dorsal habitus; f, ventral habitus.
FIGURE 5. a–c in New records of Encyrtidae (Hymenoptera: Chalcidoidea) from the Netherlands with a description of new species
FIGURE 5. a–c: Microterys seyon, female. a, dorsal habitus; b, lateral habitus; c, ventral habitus; d–f: Ooencyrtus brunneipes, female. d, dorsal habitus; e, lateral habitus; f, ventral habitus; g–i: O. gonoceri, female. g, dorsal habitus; h, lateral habitus; i, ventral habitus.
FIGURE 6. a–c in New records of Encyrtidae (Hymenoptera: Chalcidoidea) from the Netherlands with a description of new species
FIGURE 6. a–c: Parablatticida citri, female. a, dorsal habitus; b, lateral habitus; c, ventral habitus; d–f: Prionomitus tiliaris, female. d, dorsal habitus; e, lateral habitus; f, ventral habitus.
Subspecies and Distribution. A.o.oeconomusPallas,1776—W&SCSiberia(Russia)andNWMongolia. A.o.amakensisMurie,1930—AmakI(AleutianIs,Alaska). A.o.arenicoladeSélys-Longchamps,1841—Netherlands. A.o.dauricusKastschenko,1910—SCSiberia(areasaroundLakeBaikal)andNEMongolia..0.elymocetesOsgood,1906—MontagueI(SAlaska).app.0.finmarchicusSiivonen,1967—AndgyaandLanggyaintheVesteralenIs(Norway)..0.innwitusMerriam,1900—St.LawrenceI(Alaska)..0.kamtschaticusPallas,1779—KamchatkaPeninsula.Peep.0.kharanurensisCourantetal.,1999—GreatLakesHollow(NWMongolia).0.kjusjurensisKoljuschev,1935—NCSiberia..0.koreniG.M..Allen,1914—IndigirkaandKolymariverbasins(NEYakutia[=SakhaRepublic]andMagadanRegioninRussianFarEast). A.o.macfarlaniMerriam,1900—NEAlaskaandNWCanada(Yukon,NorthwestTerritories,andNunavut). A.o.mehelyiEhik,1928—SWSlovakia,EAustria,andHungary. A.o.montiumcaelestinumOgnev,1944—DzungarianAlatauandTianShan(SEKazakhstanandNWChina)..0.operariusNelson,1893—W&SAlaska..0.popofensisMerriam,1900—UngaandPopofIs(AleutianIs,Alaska).Be.0.punukensisHall&Gilmore,1932—BigPunukI(Alaska)..0.ratticepsKeyserling&Blasius,1841—FennoscandiaandNEuropeanRussia..0.sitkensisMerriam,1897—ChichagofandBaranofIs(Alaska). A.o.stimmingiNehring,1899—EGermany,Poland,Lithuania,Latvia,Belarus,Ukraine,andCEuropeanRussia. A.o.suntaricusDukelsky,1928—NW,C&SYakutia. A.o.tshuktshorumG.S.Miller,1899—ChukchiPeninsula. A.o.uchidaeKuroda,1924—N&CKurilIs. A.o.unalascensisMerriam,1897—Unalaska,UnimakandSanakIs(AleutianIs,Alaska). A. o. yakutatensis Merriam, 1900 — SW Alaska and N British Columbia. Also present on Kodiak I and small adjacentIs, and many other Aleutian Is, SW Alaska, but subspecies involved not known. in Cricetidae
Subspecies and Distribution. A.o.oeconomusPallas,1776—W&SCSiberia(Russia)andNWMongolia. A.o.amakensisMurie,1930—AmakI(AleutianIs,Alaska). A.o.arenicoladeSélys-Longchamps,1841—Netherlands. A.o.dauricusKastschenko,1910—SCSiberia(areasaroundLakeBaikal)andNEMongolia..0.elymocetesOsgood,1906—MontagueI(SAlaska).app.0.finmarchicusSiivonen,1967—AndgyaandLanggyaintheVesteralenIs(Norway)..0.innwitusMerriam,1900—St.LawrenceI(Alaska)..0.kamtschaticusPallas,1779—KamchatkaPeninsula.Peep.0.kharanurensisCourantetal.,1999—GreatLakesHollow(NWMongolia).0.kjusjurensisKoljuschev,1935—NCSiberia..0.koreniG.M..Allen,1914—IndigirkaandKolymariverbasins(NEYakutia[=SakhaRepublic]andMagadanRegioninRussianFarEast). A.o.macfarlaniMerriam,1900—NEAlaskaandNWCanada(Yukon,NorthwestTerritories,andNunavut). A.o.mehelyiEhik,1928—SWSlovakia,EAustria,andHungary. A.o.montiumcaelestinumOgnev,1944—DzungarianAlatauandTianShan(SEKazakhstanandNWChina)..0.operariusNelson,1893—W&SAlaska..0.popofensisMerriam,1900—UngaandPopofIs(AleutianIs,Alaska).Be.0.punukensisHall&Gilmore,1932—BigPunukI(Alaska)..0.ratticepsKeyserling&Blasius,1841—FennoscandiaandNEuropeanRussia..0.sitkensisMerriam,1897—ChichagofandBaranofIs(Alaska). A.o.stimmingiNehring,1899—EGermany,Poland,Lithuania,Latvia,Belarus,Ukraine,andCEuropeanRussia. A.o.suntaricusDukelsky,1928—NW,C&SYakutia. A.o.tshuktshorumG.S.Miller,1899—ChukchiPeninsula. A.o.uchidaeKuroda,1924—N&CKurilIs. A.o.unalascensisMerriam,1897—Unalaska,UnimakandSanakIs(AleutianIs,Alaska). A. o. yakutatensis Merriam, 1900 — SW Alaska and N British Columbia. Also present on Kodiak I and small adjacentIs, and many other Aleutian Is, SW Alaska, but subspecies involved not known.
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat. in Soricidae
Subspecies and Distribution. C.r.russulaHermann,1780—W&SWEuropeinGermany,Belgium,Netherlands,Luxembourg,N&WSwitzerland,France,Spain,Portugal,andmanycloseoffshoreislands.ApopulationhasbecomeestablishedonGranCanariaIintheCanaryIs,althoughwhenthespecieswaslikelyintroducedisunresolved. C. r. yebalensis Cabrera, 1913 — NW Africa in N Morocco and N Algeria. The Greater White-toothed Shrew has also been recently reported in S Ireland, where it was likely recently introduced, probably representing the subspecies russula. They also seem to have made it to Scilly Is and the Channel Is, where they probably traveled by boat.
FIGURE 2 in The taxonomy and nomenclature of Kalanchoe ×vadensis [K. blossfeldiana × K. marmorata var. somaliensis] (Crassulaceae subfam. Kalanchooideae), an early nothospecies produced in The Netherlands in the 1950s
FIGURE 2. The flowers of Kalanchoe ×kewensis are bright purplish pink and sometimes deviate from being tetramerous, the condition virtually throughout prevalent in Kalanchoe. Deviations in floral morphology are often found in hybrid kalanchoes. Photograph: Gideon F. Smith.
FIGURE 3 in The taxonomy and nomenclature of Kalanchoe ×vadensis [K. blossfeldiana × K. marmorata var. somaliensis] (Crassulaceae subfam. Kalanchooideae), an early nothospecies produced in The Netherlands in the 1950s
FIGURE 3. The holotype of the name Kalanchoe ×vadensis. The metadata associated with the specimen are: The Netherlands. Wageningen, Rijks Landbouw Hoogeschool, Institute of Horticultural Plant-breeding, ex hort., 25 February 1961, B.K. Boom 24038, (holotype L barcode L.1860830). Institution: Naturalis Biodiversity Center; Source: Naturalis—Botany catalogues. License: CC0 1.0. Reproduced with permission. https://data.biodiversitydata.nl/naturalis/specimen/L.1860830
FIGURE 4 in The taxonomy and nomenclature of Kalanchoe ×vadensis [K. blossfeldiana × K. marmorata var. somaliensis] (Crassulaceae subfam. Kalanchooideae), an early nothospecies produced in The Netherlands in the 1950s
FIGURE 4. The epitype, designated in this paper, which supports the holotype of the name Kalanchoe ×vadensis. The metadata associated with the specimen are: The Netherlands. Wageningen, Institute for Plant Breeding. In greenhouse, ex hort., 11 March 1982, J. van Veldhuizen 794, (epitype WAG [Herbarium Vadense], barcode WAG 1212259). Reproduced with permission. For attribution of the photograph see Bijmoer et al. (2021).
FIGURE 1 in The taxonomy and nomenclature of Kalanchoe ×vadensis [K. blossfeldiana × K. marmorata var. somaliensis] (Crassulaceae subfam. Kalanchooideae), an early nothospecies produced in The Netherlands in the 1950s
FIGURE 1. The harpoon-leaved Kalanchoe ×kewensis [K. bentii subsp. bentii × K. glaucescens] was one of the first artificially produced nothospecies that became widely available in the horticultural trade. Photograph: Gideon F. Smith.
Supplementary material 1 from: Zieritz A, Armas B, Aldridge D (2014) Registry of non-native species in the Two Seas region countries (Great Britain, France, Belgium and the Netherlands). NeoBiota 23: 65-80. https://doi.org/10.3897/neobiota.23.5665
Registry of non-native species in the Two Seas region countries (Great Britain, France, Belgium and the Netherlands): Explanation note: The MS Excel file contains two worksheets:
Draft genome sequences of Arabidopsis thaliana-associated micro-organisms from Reijerscamp soil, the Netherlands
<p><strong>Methodological summary and relevant references</strong></p> <p>Compressed tar archive containing 447 draft bacterial genomes and their annotations used in several studies including Fourie <em>et al</em>. (2024; in review) and Selten et al. (2024; in prep). Genome sequences are obtained by Illumina-only sequencing of microbial cultures. Illumina reads were demultiplexed and cleaned with cutadapt (version 2.8) (Martin, 2011) and assembled into genomes using A5 (A5-miseq version 20160825) (Coil et al., 2014). Genome contamination and heterogeneity was checked with CheckM (version 1.1.3) (Parks et al., 2015) and any genomes with multiple single copy gene occurrences were subjected to MaxBin (version 2.2.7) (Wu et al., 2014) to separate the genomes from contaminated bacterial cultures. Any non-bacterial contigs in the genome assemblies were removed using MMSeqs2 (version 13.45111) (Steineigger & Schöding, 2017). Open reading frames were found and annotated by PROKKA (version 1.14.6) (Seemann, 2014) and EggNOG (version 2.1.4-2) (Cantalapiedra et al., 2021) respectively. Microbial cultures were derived from <em>Arabidopsis thaliana</em> roots grown in Reijerscamp soil, described in Stringlis <em>et al</em>., 2018 https://doi.org/10.1073/pnas.1722335115.</p> <p><strong>The uploaded files are</strong></p> <ol> <li>Genome assemblies</li> <li>Prokka gene predictions in GFF3 format</li> <li>Predicted transcripts from genes in (2)</li> <li>Predicted proteins from genes in (2), and</li> <li>EggNOG annotations for the proteins in (4)</li> </ol> <p><strong>Genomes and annotations pending upload om NCBI GenBank (April 2024)</strong></p>
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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OpenNeuro
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