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1,579 results for “Baltics”
Fig. 1. A map showing 10 in New data on the distribution of ladybird beetles (Coleoptera: Coccinellidae) in the eastern part of the Baltic Coast region in Poland
Fig. 1. A map showing 10 km x 10 km grid coordinates, in which samples of Coccinellidae for this study were collected.
Fig. 2 in New data on the distribution of ladybird beetles (Coleoptera: Coccinellidae) in the eastern part of the Baltic Coast region in Poland
Fig. 2. Species composition of Coccinellidae recorded in the eastern part of the Baltic Coast in Poland on deciduous trees and shrubs (A), conifers (B), herbaceous plants (C) and beaches (D). Filled bars – contribution of the invasive Harmonia axyridis. Records of individuals without indication of the habitat where caught (228 individuals) are omitted in this calculation.
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 & 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.
An evaluation of new particle formation events in Helsinki during a Baltic Sea cyanobacterial summer bloom
<p>The data set is linked to the manuscript: Thakur, R. C., Dada, L., Beck, L. J., Quéléver, L. L. J., Chan, T., Marbouti, M., He, X.-C., Xavier, C., Sulo, J., Lampilahti, J., Lampimäki, M., Tham, Y. J., Sarnela, N., Lehtipalo, K., Norkko, A., Kulmala, M., Sipilä, M., and Jokinen, T.: An evaluation of new particle formation events in Helsinki during a Baltic Sea cyanobacterial summer bloom, Atmos. Chem. Phys. Discuss. 2022.</p>
FIGURE 2 in Spotted beauty-Gedanochila museisucini gen. et sp. nov.-a new Achilidae from Eocene Baltic amber (Hemiptera: Fulgoromorpha) and its relation to Achilini
FIGURE 2. Gedanochila museisucini gen. et sp. nov. Holotype. A, left tegmen; B, right tegmen; C, right hind wing ventral view. D, left hind wing, dorsal view. Scale bar 2 mm
FIGURE 3 in Spotted beauty-Gedanochila museisucini gen. et sp. nov.-a new Achilidae from Eocene Baltic amber (Hemiptera: Fulgoromorpha) and its relation to Achilini
FIGURE 3. Gedanochila museisucini gen. et sp. nov. Holotype. A, General dorsal view; B, General ventral view. Scale bar: 2 mm.
FIGURE 5 in Spotted beauty-Gedanochila museisucini gen. et sp. nov.-a new Achilidae from Eocene Baltic amber (Hemiptera: Fulgoromorpha) and its relation to Achilini
FIGURE 5. Gedanochila museisucini gen. et sp. nov. Paratype. A, General dorsal view. B, Anterior portion of body, laterodorsal view; C, Ventral view; D, Face and rostrum; E, Metatarsi. Scale bar 2 mm for A, C, 1 mm for B, D, E.
FIGURE 4 in Spotted beauty-Gedanochila museisucini gen. et sp. nov.-a new Achilidae from Eocene Baltic amber (Hemiptera: Fulgoromorpha) and its relation to Achilini
FIGURE 4. Gedanochila museisucini gen. et sp. nov. Holotype. A, Face; B, Apex of right metatibia and metatarasus; C, Right metatarsus; D, Left metatarsus; E-H, Anaglyph images of the specimen in dorsal view. Scale bars: 0.5 mm for A-D; 2 mm for E-H.
FIGURE 1 in Spotted beauty-Gedanochila museisucini gen. et sp. nov.-a new Achilidae from Eocene Baltic amber (Hemiptera: Fulgoromorpha) and its relation to Achilini
FIGURE 1. Gedanochila museisucini gen. et sp. nov. Holotype. A, Anterior portion of body in dorsal view; B, Head capsule in frontal view; C, Head capsule in frontolateral view; D, Tip of metatibia and metatarsus. Scale bar 1 mm.
Subspecies and Distribution. P. h. hispida Schreber, 1775 — Arctic Ocean. P h. botnica Gmelin, 1788 — Baltic Sea. P. h. ladogensis Nordqvist, 1889 — Lake Ladoga (W Russia). Ph. ochotensis Pallas, 1811 — Sea of Okhotsk and N Japan (Hokkaido). P. h. saimensis Nordqvist, 1889 — Lake Saimaa (S Finland). in Phocidae
Subspecies and Distribution. P. h. hispida Schreber, 1775 — Arctic Ocean. P h. botnica Gmelin, 1788 — Baltic Sea. P. h. ladogensis Nordqvist, 1889 — Lake Ladoga (W Russia). Ph. ochotensis Pallas, 1811 — Sea of Okhotsk and N Japan (Hokkaido). P. h. saimensis Nordqvist, 1889 — Lake Saimaa (S Finland).
Distribution. Cold temperate to subarctic waters of the N Atlantic Ocean (including mouth of the Saint Lawrence River, Canada, but excluding the Baltic Sea), S to ¢.38° N in W Atlantic Ocean, and from S Svalbard to the Brittany coast, France, in the E Atlantic Ocean. in Delphinidae
Distribution. Cold temperate to subarctic waters of the N Atlantic Ocean (including mouth of the Saint Lawrence River, Canada, but excluding the Baltic Sea), S to ¢.38° N in W Atlantic Ocean, and from S Svalbard to the Brittany coast, France, in the E Atlantic Ocean.
Distribution. Temperate to subarctic waters of the N Atlantic including S Davis Strait, Gulf of Saint Lawrence, Barents Sea, and North Sea, S to Cape Cod (USA) in the E and the coasts of N France in the W. Extralimital sightings in the Baltic Sea, Bay of Biscay, and Iberian Peninsula. in Delphinidae
Distribution. Temperate to subarctic waters of the N Atlantic including S Davis Strait, Gulf of Saint Lawrence, Barents Sea, and North Sea, S to Cape Cod (USA) in the E and the coasts of N France in the W. Extralimital sightings in the Baltic Sea, Bay of Biscay, and Iberian Peninsula.
Subspecies and Distribution. L.e.europaeusPallas,1778—WesternEurope. L. e. caspicus Hemprich & Ehrenberg, 1832 — Lower Volga, Kalmykia (Russia) and W Kazakhstan. JR e. connor Robinson, 1918 — NW Iran. e. creticus Barrett-Hamilton, 1903 — Crete (Greece). a e. cyprius Barrett-Hamilton, 1903 — Cyprus. e. cyrensis Satunin, 1905 — Azerbaijan, Transcaucasia. a e. hybridus Desmarest, 1822 — Baltic States, Belarus, Ukraine, Finland, W & C Russia. Sl e. judeae Gray, 1867 — Palestine. aE e. karpathorum Hilzheimer, 1906 — Carpathian Mts. all e. medius Nilsson, 1820 — Denmark. al e. occidentalis de Winton, 1898 — Great Britain. ul e. parnassius Miller, 1903 — C Greece. el. e. ponticus Ognev, 1929 — Black Sea coast (Russia). ul. e. rhodius Festa, 1914 — Rhodes (Greece). Bl e. syriacus Hemprich & Ehrenberg, 1832 — Syria. ab. e. transsylvanicus Matschie, 1901 — E & SE Europe. in Leporidae
Subspecies and Distribution. L.e.europaeusPallas,1778—WesternEurope. L. e. caspicus Hemprich & Ehrenberg, 1832 — Lower Volga, Kalmykia (Russia) and W Kazakhstan. JR e. connor Robinson, 1918 — NW Iran. e. creticus Barrett-Hamilton, 1903 — Crete (Greece). a e. cyprius Barrett-Hamilton, 1903 — Cyprus. e. cyrensis Satunin, 1905 — Azerbaijan, Transcaucasia. a e. hybridus Desmarest, 1822 — Baltic States, Belarus, Ukraine, Finland, W & C Russia. Sl e. judeae Gray, 1867 — Palestine. aE e. karpathorum Hilzheimer, 1906 — Carpathian Mts. all e. medius Nilsson, 1820 — Denmark. al e. occidentalis de Winton, 1898 — Great Britain. ul e. parnassius Miller, 1903 — C Greece. el. e. ponticus Ognev, 1929 — Black Sea coast (Russia). ul. e. rhodius Festa, 1914 — Rhodes (Greece). Bl e. syriacus Hemprich & Ehrenberg, 1832 — Syria. ab. e. transsylvanicus Matschie, 1901 — E & SE Europe.
Genome-wide signatures of synergistic epistasis during parallel adaptation in a Baltic Sea copepod
<p>The role of epistasis in adaptive evolution has remained an unresolved problem dating back to the Evolutionary Synthesis. This role is now being revisited due to its relevance for polygenic adaptation. In the absence of epistasis, polygenic adaptation is predicted to result in non-parallel evolution, because repeated selection could act on subsets of effectively redundant alleles. However, positive epistatic interactions among adaptive alleles would make the alleles non-redundant and selection for particular allelic combinations could drive parallel evolution. The inability to address this fundamental question might arise from traditional approaches lacking the power to capture the genomic architecture and dynamics of polygenic adaptation. To address this problem, we employed a replicated and controlled evolution experiment using the copepod <em>Eurytemora affinis</em> to elucidate the evolutionary response architecture to rapid salinity decline, a predicted consequence of global climate change in higher latitudes. Based on time-resolved pooled whole-genome sequencing, we uncovered a remarkably parallel response, despite polygenic adaptation involving over 1000 loci across ten replicate selection lines. Interestingly, single-nucleotide polymorphism (SNP) frequencies converged during the experiment, far beyond expectations, resulting in replicate lines sharing 93.1% of selected alleles. Using simulations, we found that this polygenic parallelism was consistent with synergistic epistasis among alleles responding in concert across replicate lines, a phenomenon that may be common for selection on complex physiological traits. Furthermore, we found that the same SNPs with signatures of selection in the laboratory also exhibited signatures of selection across a natural salinity gradient in the Baltic Sea. Our study provides the first experimental evidence that polygenic adaptation can actually be highly repeatable at the genomic level, given the presence of synergistic epistasis among the loci under selection.</p>
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I. in Talpidae
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I.
Distribution. Great Britain, C Europe, and Scandinavia, and across E Europe, Anatolia, Caucasus, NW Iran, and Kazakhstan to Siberia (E to Lake Baikal and Lena River), extreme N Mongolia (Mongolian Altai and Hovsgol Mts), and NE China (N Xinjiang); also present on many islands and islets in Baltic and North seas. in Cricetidae
Distribution. Great Britain, C Europe, and Scandinavia, and across E Europe, Anatolia, Caucasus, NW Iran, and Kazakhstan to Siberia (E to Lake Baikal and Lena River), extreme N Mongolia (Mongolian Altai and Hovsgol Mts), and NE China (N Xinjiang); also present on many islands and islets in Baltic and North seas.
FIGURES 6–8 in Eustrophus praecursor sp. nov.: the first Eocene species of Eustrophinae (Coleoptera: Tetratomidae) from Baltic amber
FIGURES 6–8. Cenozoic representatives of Eustrophus: 6—distribution of extant species (green area) and Eocene record of E. praecursor sp. nov. (red dot); 7—extant European E. dermestoides in the natural habitat from the Sambian Peninsula (Kaliningrad region, Russia), 26 May 2021, dorso-frontal view; 8—ibidem, dorso-lateral view.
FIGURES 1–2 in Eustrophus praecursor sp. nov.: the first Eocene species of Eustrophinae (Coleoptera: Tetratomidae) from Baltic amber
FIGURES 1–2. Eustrophus praecursor sp. nov., holotype, No 6819 [MAIG]: 1—habitus, dorsal view; 2—habitus, ventral view. Scale bar = 1.0 mm.
FIGURE 3 in Two new fossil species of soldier beetles (Coleoptera, Cantharidae, Malthininae) from Baltic amber
FIGURE 3. Malthodes (Malthodes) markpankowskii sp. nov. A: Holotype, habitus, dorsal view, scale bar = 0.5 mm. B: Holotype, habitus, detail of metasternum, scale bar = 0.2 mm. C: Holotype, habitus, ventral view, scale bar = 1.0 mm. D: Holotype, habitus, ventral view (detail), scale bar = 0.5 mm.
FIGURE 2 in Two new fossil species of soldier beetles (Coleoptera, Cantharidae, Malthininae) from Baltic amber
FIGURE 2. Malthinus (Malthinus) masoni sp. nov. A: Holotype, habitus, ventral view, scale bar = 1.0 mm. B: Holotype, habitus, ventral view (detail), scale bar = 0.5 mm.
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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.