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Comparison of native and non-native predator consumption rates and prey avoidance behavior in North America and Europe
<p>Novel predator-prey interactions can contribute to the invasion success of non-native predators. For example, native prey can fail to recognize and avoid non-native predators due to a lack of co-evolutionary history and cue dissimilarity with native predators. This might result in a competitive advantage for non-native predators. Numerous lady beetle species were globally redistributed as biological control agents against aphids, resulting in novel predator-prey interactions. Here, we investigated the strength of avoidance behavior of the pea aphid (<i>Acyrthosiphon pisum</i>) towards chemical cues of native lady beetles and non-native Asian <i>Harmonia axyridis</i> and European <i>Coccinella</i><i> septempunctata </i>and <em>Hippodamia variegata</em> in North America, hypothesizing that cues of non-native lady beetles induce weaker avoidance behavior than cues of co-evolved native lady beetles. Additionally, we compared aphid consumption of lady beetles, examining potential predation advantages of non-native lady beetles. Finally, we compared cue avoidance behavior between North American and European pea aphid populations and aphid consumption of native and non-native lady beetles in North America and Europe. In North America, pea aphids avoided chemical cues of all ladybeetle species tested, regardless of their origin. In contrast to pea aphids in North America, European pea aphids did not avoid cues of the non-native <i>H. axyridis.</i> The non-native <i>H. axyridis</i> and <i>C. septempunctata</i> were among the largest and most voracious lady beetle species tested, on both continents. Consequently, in North America non-native lady beetle species might have a competitive advantage on shared food resources due to their relatively large body size, compared to several native American lady beetle species. In Europe, however, non-native <i>H. axyridis</i> might benefit from missing aphid cue avoidance as well as a large body size. The co-evolutionary time gap between the European and North American invasion of <i>H. axyridis</i>, likely explains the intercontinental differences in cue avoidance behavior and might indicate evolution in aphids towards non-native predators.</p>
Figure 1 from: Doorenweerd C, van Haren M, Schermer M, Pieterse S, van Nieukerken E (2014) A Linnaeus NGTM interactive key to the Lithocolletinae of North-West Europe aimed at accelerating the accumulation of reliable biodiversity data (Lepidoptera, Gracillariidae). ZooKeys 422: 87-101. https://doi.org/10.3897/zookeys.422.7446
Figure 1 - Screenshot of the user interface with different sections indicated. 1 Search by name 2 search by character 3 main window with resulting selection, a more information, links to respective species page on fauna europaea b distinctive characters, becomes visible with a selection of 8 or less c displays species with a similar appearance.
QuantMig survey on the future of migration between Europe and the Middle East & North Africa
<p>Data generated by the QuantMig survey on the future of migration between Europe and the Middle East & North Africa, based on the assessment of 138 migration experts.</p> <p>Detailed <strong>information about the survey</strong> can be found in:</p> <p>Boissonneault, M., Costa, R. and de Valk, H.A.G. (2022). The future of migration between Europe and the Middle East & North Africa under scenarios of social change: a factorial survey among European migration professionals. QuantMig Project Deliverable D7.2. The Hague: Netherlands Interdisciplinary Demographic Institute (NIDI)- KNAW/University of Groningen.<br> Available at <a href="http://quantmig.eu/res/files/QuantMig_Deliverable%207.2%20v1.1.pdf">http://quantmig.eu/res/files/QuantMig_Deliverable%207.2%20v1.1.pdf</a></p> <p>A <strong>guide to the datasets</strong> can be found in:</p> <p>Boissonneault, M., Costa, R. (2022). QuantMig survey on the future of migration: guide to the generated databases. QuantMig Project Deliverable D7.3. The Hague: Netherlands Interdisciplinary Demographic Institute (NIDI)-KNAW/University of Groningen.<br> Available at <a href="http://quantmig.eu/res/files/QuantMig_Deliverable%207.3%20v1.2.pdf">http://quantmig.eu/res/files/QuantMig_Deliverable%207.3%20v1.2.pdf</a></p>
Supplementary material 1 from: Tietz B, Penner J, Vamberger M (2023) Chelonian challenge: three alien species from North America are moving their reproductive boundaries in Central Europe. NeoBiota 82: 1-21. https://doi.org/10.3897/neobiota.82.87264
Supplementary information
The TRAfermin in Neuropathic Diabetic Foot Ulcer Study - Northern Europe The TRANS-North Study
ClinicalTrials.gov study NCT01217476. IPD Sharing: Not stated. Countries: 10. Publications: 0.
Comparison of native and non-native predator consumption rates and prey avoidance behavior in North America and Europe
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Data from: Spring predictability explains different leaf-out strategies in the woody floras of North America, Europe and East Asia
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Spatio-temporal variability of tidal-stream energy in north-western Europe
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Figure 1 in Reassessment of molecular and morphological variation within the Anagrus atomus species complex (Hymenoptera: Mymaridae): egg parasitoids of leafhoppers (Hemiptera: Cicadellidae) in Europe and North America
Figure 1. Relationships among species of the Anagrus atomus complex, inferred from ML analysis of a 345bp sequence of the COI gene. Analyses were conducted in RAxML with the GTR + Γ + I model and data partitioning by third codon position. Support for the major branches, expressed as a percentage, was assessed with 1000 rapid bootstrap replicates. Scale bar represents substitutions per nucleotide site. PR numbers relate to GenBank accessions MW012433–MW012491.
FIGURE 5. Coprinopsis alnivora. A in Coprinopsis alnivora (Psathyrellaceae), a rare species from North America is discovered in Europe
FIGURE 5. Coprinopsis alnivora. A. Hyphae of universal veil. B. Secondary mycelium. C. Pleurocystidia. Scale bars = 20 μm. Drawings by: J. Červenka.
FIGURE 18 in The Rhyacophila fasciata Group in Europe: Rhyacophila macedonica Karaouzas Valladolid & Ibrahimi (n. sp.) from Greece, Kosovo, Republic of North Macedonia and Serbia (Trichoptera: Rhyacophilidae)
FIGURE 18. Phylogenetic relationship among the species of the Rhyacophila fasciata Group included in this study. Combination of bayesian phylogenetic and maximum likelihood trees based on COI. Support for each node is represented by the posterior probabilities (PP) resulting from the Bayesian inference analysis and the bootstrap support values (BS) obtained for the maximum likelihood tree (PP/BS). Rhyacophila cf. obliterata (Robl) (18a), outgroup; Rhyacophila fasciata Group: Rhyacophila kykladica Malicky & Sipahiler 1993 (Rkyk) (18b), Rhyacophila macedonica Karaouzas, Valladolid & Ibrahimi (n. sp.) (Rmac) (18c), Rhyacophila fasciata Hagen 1859 (Rfas) (18d), Rhyacophila denticulata McLachlan 1879 (Rden) (18e), Rhyacophila sociata Navás 1916 (Rsoc) (18f), Rhyacophila fasciata viteceki Valladolid & Kučinić 2020 (in Valladolid et al. 2020) (Rfvit) (18g), Rhyacophila fasciata delici Kučinić & Valladolid (in Valladolid et al. 2020) (Rfdel) (18h), Rhyacophila septentrionis McLachlan 1865 (Rsep) (18i). Data for specimens are summarized in Table 1. Countries: BEL = Belgium, BAH = Bosnia and Herzegovina, CRO = Croatia, CZE = Czech Republic, EST = Estonia, FIN = Finland, FRA = France, GER = Germany, GRE = Greece, KOS = Kosovo, MAC = North Macedonia, NOR = Norway, POL = Poland, RUS = Russia, SER = Serbia, SLO = Slovakia, SPA = Spain, UK = United Kingdom. Scale bar: mean number of nucleotide substitutions per site or nucleotide position on the respective branch.
FIGURES 2–6 in The Rhyacophila fasciata Group in Europe: Rhyacophila macedonica Karaouzas Valladolid & Ibrahimi (n. sp.) from Greece, Kosovo, Republic of North Macedonia and Serbia (Trichoptera: Rhyacophilidae)
FIGURES 2–6. Larva of Rhyacophila macedonica Karaouzas, Valladolid & Ibrahimi (n. sp.). 2a–2e, head: 2a, dark coloration, dorsal; 2b, dark coloration, right lateral; 2c, pale coloration, dorsal; 2d, pale coloration, right lateral; 2e, frontoclypeus, dorsal. 3D–3V, mandibles from last instar larval exuviae, left (l) and right (r): 3D, dorsal; 3V, ventral. 4a–4b, prothorax: 4a, dorsal; 4b, left hemisclerite, left lateral. 5, abdominal tergite IX. 6a–6c, details of anal prolegs: 6a, right anal claw, right lateral; 6b, detail of basolateral plate with sword process and basoventral hook, right lateral; 6c, detail of right claw, right lateral. Scale bars: unlabelled = 1 mm; ● = 0.5 mm.
FIGURES. 41–48. 41 in The species of Eilema Hübner, [1819] sensu lato present in Europe and North Africa (Lepidoptera: Erebidae: Arctiinae: Lithosiini)
FIGURES. 41–48. 41. Katha depressa (Esper, [1787]). Male: Riera del Surreig, Osona (Barcelona), 26.vi.2002, R. Macià & J. Ylla leg.; 42. Female: Santuari de Puiglagulla, Vilalleons, Osona (Barcelona), 7.viii.2006, R. Macià leg.; 43. Wittia sororcula (Hufnagel, 1766). Male: Loma del Rey, Quintanilla Sobresierra (Burgos) Spain, 1050 m, 30TVN41, 28.v.2008, R. Macià leg.; 44. Female: Serra del Turmell, Vallibona (Castellò) Spain, 1080 m, 2.viii.2007, R. Macià & J.Ylla leg.; 45. Pseudokatha rungsi Toulgoët, 1960. Male: Camino de Murguis, Las Entinas, Almerimar (Almería), 4 m, 12.vi.2014, R. Macià leg.; 46. Female: Platja Cuartel Vell, Torre la Sal (Castellón), 3 m, 31TBE54, 5.v.2011, R. Macià leg.; 47. Zobida bipuncta (Hübner, [1824]).Male: P.N de Doñana (Huelva) Spain, 10 m, 2.x.2019 R. Macià leg., 48. Female: P. N. de Doñana (Huelva) Spain, 10 m, 2.x.2019 R. Macià leg.
PLATE 13 in Type material of land snails (Mollusca: Gastropoda) described from New Zealand by taxonomists in Europe and North America between 1830 and 1934, and the history of research on the New Zealand land snail fauna from 1824 to 1917
PLATE 13. Reproductions of previous illustrations. Athoracophoridae and Milacidae. A, Limax bitentaculatus Quoy & Gaimard, 1832: 148, pl. 13, figs. 1, 2, Tasman Bay, holotype, dimensions not stated; B, Janella schauinslandi Plate, 1898: 193, pl. 12, figs. 1, 2, Stephens Island, syntype (length 44 mm, width 11 mm); C, Limax fuliginosus Gould, 1852: 5, Gould (1856: pl. 1, fig. 4), Bay of Islands, syntype (length 63.5 mm).
PLATE 4. Charopidae. A in Type material of land snails (Mollusca: Gastropoda) described from New Zealand by taxonomists in Europe and North America between 1830 and 1934, and the history of research on the New Zealand land snail fauna from 1824 to 1917
PLATE 4. Charopidae. A, Zonites coma Gray, 1843, New Zealand, lectotype, NHMUK 1842.11.5.141; B, Helix coma var. β Pfeiffer, 1853, New Zealand, NHMUK 20130107; C, Helix compressivoluta Reeve, 1852 syntype [= Helix omega Pfeiffer, 1853 syntype], New Zealand, NHMUK 1996113; D, Helix crebriflammea Reeve, 1852 syntype [= Helix crebriflammis Pfeiffer, 1853 syntype], New Zealand, NHMUK 20140671; E, Helix dimorpha Reeve, 1852 lectotype [= Helix dimorpha Pfeiffer, 1853 syntype], New Zealand, NHMUK192729/1; F, Helix egesta Gray, 1850, Auckland, syntype, NHMUK 1849.12.3.75–78 & 1850.12.28.504–508.
PLATE 7. Charopidae. A in Type material of land snails (Mollusca: Gastropoda) described from New Zealand by taxonomists in Europe and North America between 1830 and 1934, and the history of research on the New Zealand land snail fauna from 1824 to 1917
PLATE 7. Charopidae. A, Helix (Patula) stokesi Smith, 1884, Wairarapa, lectotype, NHMUK 1884.6.12.646; B, Helix tau Pfeiffer, 1861, Kaikoura, neotype [= holotype of Fectola trilamellata Climo, 1978], NMNZ M.47445; C, Helix (Thalassia) traversi Smith, 1884, Wairarapa, syntype, NHMUK 1884.6.12.644–645; D, Allodiscus tullia Marshall & Barker, 2008 (non Gray, 1850), New Zealand, 'lectotype', NHMUK 1849.12.22.128; E, Helix venulata Pfeiffer, 1857, New Zealand, lectotype, NHMUK 1996150/1. Euconulidae. F, Trocho-Nanina exposita Mousson, 1873, Kermadec Islands, syntype, ZMZ 501943. Helicarionidae. G, Vitrina ultima Mousson, 1873, Sunday [Raoul] Island, syntype, ZMZ 500934.
PLATE 12 in Type material of land snails (Mollusca: Gastropoda) described from New Zealand by taxonomists in Europe and North America between 1830 and 1934, and the history of research on the New Zealand land snail fauna from 1824 to 1917
PLATE 12. Reproductions of previous illustrations. Achatinellidae. A, Tornatellina novoseelandica Küster, 1852: 149, pl. 18, fig. 11, New Zealand, syntype (Höhe 1 2/ ''', Breite 2/ ''', = c. 3.05 x 1.45 mm); B, Tornatellides subperforatus kermadecensis 5 3 Pilsbry & Cooke, 1915: 200, pl. 44, fig. 16, Raoul Island, holotype, ANSP 8315 (2.5 x 1.5 mm); C, Tornatellina kermadecensis Pilsbry & Cooke, 1915: 149, pl. 39, figs. 1–5, Sunday [Raoul] Island, holotype? (3.3 x 1.6 mm); D, Tornatellina (Tornatellinops) iredalei Pilsbry & Cooke, 1915: 180, pl. 39, figs. 6–8, Sunday [Raoul] Island, holotype? (2.9 x 1.5 mm); E, Tornatellina (Tornatellinops) raoulensis Pilsbry & Cooke, 1915: 180, pl. 39, figs. 9–11, Raoul Island, holotype? (3.3 x 1.7 mm).
PLATE 3. Charopidae. A in Type material of land snails (Mollusca: Gastropoda) described from New Zealand by taxonomists in Europe and North America between 1830 and 1934, and the history of research on the New Zealand land snail fauna from 1824 to 1917
PLATE 3. Charopidae. A, Nanina? celinde Gray, 1850, Auckland, lectotype, NHMUK 1849.12.3.86; B, Helix fatua Pfeiffer, 1857, New Zealand, syntype, NHMUK 1974128; C, Helix chimmoi Pfeiffer, 1857, Sunday [Raoul] Island, lectotype, NHMUK 1962709/1; D, Patula modicella var. vicinalis Mousson, 1873, Sunday [Raoul] Island, syntype, ZMZ 503025; E, Helix buccinella Reeve, 1852 syntype [= Helix gamma Pfeiffer, 1853 syntype], New Zealand, NHMUK 1996017; F, Zonites chiron Gray, 1850, Auckland, lectotype, NHMUK 1849.12.3.71; G, Helix collyrula Reeve, 1852 syntype [= Helix kappa Pfeiffer, 1853 syntype], New Zealand, NHMUK 20140670.
PLATE 11. Species not from New Zealand. A in Type material of land snails (Mollusca: Gastropoda) described from New Zealand by taxonomists in Europe and North America between 1830 and 1934, and the history of research on the New Zealand land snail fauna from 1824 to 1917
PLATE 11. Species not from New Zealand. A, Helix pachystyla Pfeiffer, 1845, syntype, NHMUK 1982233; B, Helix reinga Pfeiffer, 1846, syntype, NHMUK 197019; C, Helix guttula Pfeiffer, 1853, syntype, NHMUK 20160063/1; D, Helix regularis Reeve, 1854 syntype [= Helix regularis Pfeiffer, 1855 lectotype], NHMUK 20141112; E, Helix subrugata Reeve, 1852 syntype [= Helix subrugata Pfeiffer, 1853 syntype], NHMUK 1982236; F, Helix rapida Pfeiffer, 1853, syntype, NHMUK 1998173.
PLATE 10. Species not from New Zealand. A in Type material of land snails (Mollusca: Gastropoda) described from New Zealand by taxonomists in Europe and North America between 1830 and 1934, and the history of research on the New Zealand land snail fauna from 1824 to 1917
PLATE 10. Species not from New Zealand. A, Hydrocena (Omphalotropis) vestita Pfeiffer, 1855, syntype, NHMUK 20160068; B, Omphalotropis conella Sykes, 1902, Port Vila, Efate, syntype, NHMUK 1902.12.1.260.
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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.