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Subspecies and Distribution. P. t. trinitatis G. S. Miller, 1899 - recorded in most of Venezuela, the Guianas, and N, NE & Brazil, also on several Caribbean Is (Aruba, Margarita, Trinidad, and Tobago). P. t. phaea G. M. Allen, 1911 — restricted to Grenada I. in Emballonuridae
Subspecies and Distribution. P. t. trinitatis G. S. Miller, 1899 - recorded in most of Venezuela, the Guianas, and N, NE & Brazil, also on several Caribbean Is (Aruba, Margarita, Trinidad, and Tobago). P. t. phaea G. M. Allen, 1911 — restricted to Grenada I.
Marlim R3D (MR3D) - Extended Resistivity Model (100 x 100 x 20 m mesh)
<p>Marlim R3D (MR3D) is an open-source realistic geoelectric model for CSEM simulations of the post-salt turbiditic reservoirs at the Brazilian offshore margin.<br> Here we make available the Marlim MR3D model with a 100 x 100 x 20 m mesh extended to a volume of 56 x 51 x 6 km. That extended model was used by Correa and Menezes (2019) to produce the two CSEM dataset available at https://doi.org/10.5281/zenodo.1807135 (noise-free) and http://doi.org/10.5281/zenodo.1256787 (1% added noise).<br> You can follow the updates of the marlim project at:<br> https://www.researchgate.net/project/Marlim-R3D-A-realistic-model-for-mCSEM-simulations<br> Correa, J. L., and Menezes, P. T. L., 2019. Marlim R3D: A realistic model for controlled-source electromagnetic simulations — Phase 2: The controlled-source electromagnetic data set. Geophysics, 84 (5), E293–E299.</p> <p> </p> <p>Mrl3d_Rh_20metersmesh.segy - horizontal resistivity</p> <p>Mrl3d_Rv_20metersmesh.segy - vertical resistivity</p>
Supplementary material 1 from: Dickey JWE, Cuthbert RN, South J, Britton JR, Caffrey J, Chang X, Crane K, Coughlan NE, Fadaei E, Farnsworth KD, Ismar-Rebitz SMH, Joyce PWS, Julius M, Laverty C, Lucy FE, MacIsaac HJ, McCard M, McGlade CLO, Reid N, Ricciardi A, Wasserman RJ, Weyl OLF, Dick JTA (2020) On the RIP: using Relative Impact Potential to assess the ecological impacts of invasive alien species. NeoBiota 55: 27-60. https://doi.org/10.3897/neobiota.55.49547
Table S1. Outline of different numerical response proxies available, guidance for their use and the advantages and disadvantages of each
Subspecies and Distribution. R. p. perniger Hodgson, 1843 - N, C & SW India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, Nagaland, Madhya Pradesh, Karnataka, and Kerala), C & E Nepal, Bhutan, Bangladesh, Myanmar, S China (Yunnan), N Thailand, Laos, Vietnam, and Cambodia. . p. lanosus K. Andersen, 1905 — C & SE China (Sichuan, Guizhou, Guangxi, Anhui Zhejiang,Jiangxi, Fujian, and Guangdong). R.p. spurcus G. M. Allen, 1928 - Hainan I, China. Possibly also peninsular Thailand, according to recorded calls. in Rhinolophidae
Subspecies and Distribution. R. p. perniger Hodgson, 1843 - N, C & SW India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, Nagaland, Madhya Pradesh, Karnataka, and Kerala), C & E Nepal, Bhutan, Bangladesh, Myanmar, S China (Yunnan), N Thailand, Laos, Vietnam, and Cambodia. . p. lanosus K. Andersen, 1905 — C & SE China (Sichuan, Guizhou, Guangxi, Anhui Zhejiang,Jiangxi, Fujian, and Guangdong). R.p. spurcus G. M. Allen, 1928 - Hainan I, China. Possibly also peninsular Thailand, according to recorded calls.
Subspecies and Distribution. R.p. pusillus Temminck, 1834 - N Sumatra, N, E & S Borneo (including Banggi I), W Java, and Bali I. R. p. blythi K. Andersen, 1918 - N India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, and Arunachal Pradesh), Nepal, Bhutan, and SE Bangladesh. R.p. calidusG. M. Allen, 1923-SE China (Guizhou, Guangxi, Guangdong, and Fujian, along with a recent record from Beijing area that may represent this subspecies). R. p. gracilis K. Andersen, 1905 - S India (Andhra Pradesh, Karnataka, Kerala, and Tamil Nadu). R.p. lakkhanae Yoshiyuki, 1990 - S China (Yunnan), Thailand, Laos, Vietnam (including Cat Ba I), Cambodia, and Peninsular Malaysia (including Tioman I). R.p. minutillusG. S. Miller, 1906 —Anambas Is (Siantan). R.p. pagi Tate & Archbold, 1939 — Mentawai Is (North Pagai). R.p. parcus G. M. Allen, 1928 - Hainan I, China. R. p. szechwanus K Andersen, 1918 - Myanmar and C China (Sichuan, Guizhou, Hubei, and probably Yunnan). in Rhinolophidae
Subspecies and Distribution. R.p. pusillus Temminck, 1834 - N Sumatra, N, E & S Borneo (including Banggi I), W Java, and Bali I. R. p. blythi K. Andersen, 1918 - N India (Uttarakhand, Sikkim, West Bengal, Assam, Meghalaya, and Arunachal Pradesh), Nepal, Bhutan, and SE Bangladesh. R.p. calidusG. M. Allen, 1923-SE China (Guizhou, Guangxi, Guangdong, and Fujian, along with a recent record from Beijing area that may represent this subspecies). R. p. gracilis K. Andersen, 1905 - S India (Andhra Pradesh, Karnataka, Kerala, and Tamil Nadu). R.p. lakkhanae Yoshiyuki, 1990 - S China (Yunnan), Thailand, Laos, Vietnam (including Cat Ba I), Cambodia, and Peninsular Malaysia (including Tioman I). R.p. minutillusG. S. Miller, 1906 —Anambas Is (Siantan). R.p. pagi Tate & Archbold, 1939 — Mentawai Is (North Pagai). R.p. parcus G. M. Allen, 1928 - Hainan I, China. R. p. szechwanus K Andersen, 1918 - Myanmar and C China (Sichuan, Guizhou, Hubei, and probably Yunnan).
Subspecies and Distribution. R m. mehelyi Matschie, 1901 - S Europe (S Iberian Peninsula, Sardinia, E Sicily, SE Italy, S Albania, E Serbia, S Romania, E North Macedonia, Bulgaria, and Greece), SW Asia (Caucasus, Anatolia, N Iraq, and Zagros Mts in W Iran), and N Africa (N Morocco, N Algeria, and N Tunisia); possibly a record from SE France, and there are apparently records from Afghanistan, although exact localities are uncertain. R m. judaicus K. Andersen & Matschie, 1904 - Levant in Cyprus, N Syria, W Jordan, Israel, NE Egypt (including NW Sinai based on echolocation), and NE Libya. in Rhinolophidae
Subspecies and Distribution. R m. mehelyi Matschie, 1901 - S Europe (S Iberian Peninsula, Sardinia, E Sicily, SE Italy, S Albania, E Serbia, S Romania, E North Macedonia, Bulgaria, and Greece), SW Asia (Caucasus, Anatolia, N Iraq, and Zagros Mts in W Iran), and N Africa (N Morocco, N Algeria, and N Tunisia); possibly a record from SE France, and there are apparently records from Afghanistan, although exact localities are uncertain. R m. judaicus K. Andersen & Matschie, 1904 - Levant in Cyprus, N Syria, W Jordan, Israel, NE Egypt (including NW Sinai based on echolocation), and NE Libya.
Supplementary material 1 from: Ollivier M, Kazakou E, Corbin M, Sartori K, Gooden B, Lesieur V, Thomann T, Martin J-F, Tixier MS (2020) Trait differentiation between native and introduced populations of the invasive plant Sonchus oleraceus L. (Asteraceae). NeoBiota 55: 85-115. https://doi.org/10.3897/neobiota.55.49158
Table S1. Location and climatic data for the 14 Sonchus oleraceus populations used for offspring comparisons under standardised conditions
Supplementary material 4 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Figure S1. Mean plant volume ± se of A. artemisiifolia plants measured during the experiment in the four experimental sites
Supplementary material 2 from: Ollivier M, Kazakou E, Corbin M, Sartori K, Gooden B, Lesieur V, Thomann T, Martin J-F, Tixier MS (2020) Trait differentiation between native and introduced populations of the invasive plant Sonchus oleraceus L. (Asteraceae). NeoBiota 55: 85-115. https://doi.org/10.3897/neobiota.55.49158
Table S2. Mean (± standard error) values for 20 traits assessed for native (Europe and North Africa) and invasive (Australia and New Zealand) populations of Sonchus oleraceus under standardised conditions
Supplementary material 3 from: Ollivier M, Kazakou E, Corbin M, Sartori K, Gooden B, Lesieur V, Thomann T, Martin J-F, Tixier MS (2020) Trait differentiation between native and introduced populations of the invasive plant Sonchus oleraceus L. (Asteraceae). NeoBiota 55: 85-115. https://doi.org/10.3897/neobiota.55.49158
Table S3. Results of mixed models assessing the effect of range (native: Europe and North Africa, introduced: Australia and New Zealand), population within range being considered as a random factor, for 20 plants traits measured on Sonchus oleraceus under standardised conditions
FIGURE 17. Sthenaster emmae. A. Central Plateau scarp, 870 m. B. Central Plateau Scarp, 874 m C. Central Plateau Scarp, 865 m D in New species, occurrence records and observations of predation by deep-sea Asteroidea (Echinodermata) from the North Atlantic by NOAA ship Okeanos Explorer
FIGURE 17. Sthenaster emmae. A. Central Plateau scarp, 870 m. B. Central Plateau Scarp, 874 m C. Central Plateau Scarp, 865 m D. Richardson's Jellyfish, 865 m
Supplementary material 1 from: Takács A, Szabóky C, Tóth B, Bozsó M, Kutas J, Molnár S, Richter I (2020) Nearctic walnut leafminers invade Europe: first Coptodisca lucifluella (Clemens, 1860) and now Coptodisca juglandiella (Chambers, 1874) (Lepidoptera, Heliozelidae). Nota Lepidopterologica 43: 77-93. https://doi.org/10.3897/nl.43.38686
Table S1. Nearctic walnut leafminers invade Europe: First Coptodisca lucifluella (Clemens. 1860) and now C. juglandiella (Chambers. 1874) (Lepidoptera: Heliozelidae)
FIGURE 20. Velatida. A. Remaster palmatus. Stetson Mesa Terrace, 445.4 m. B in New species, occurrence records and observations of predation by deep-sea Asteroidea (Echinodermata) from the North Atlantic by NOAA ship Okeanos Explorer
FIGURE 20. Velatida. A. Remaster palmatus. Stetson Mesa Terrace, 445.4 m. B. Large specimen (30.0 cm total diameter) of Pythonaster atlantidis, NW Florida Escarpment, 1970 m. C and D. Pythonaster atlantidis sponge predation. DeSoto Canyon, 2604 m, showing dorsal and oral views (C&D respectively). E. Feeding on hexactinellid sponge. Jaguey Spur, off Puerto Rico, 2668 m. Feeding.
FIGURES 10–11. M in Revision of the Metallactus hamifer species-group (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 10–11. M. luniger (10), M. madefactus (11). 10a–b: habitus; 10c–e: median lobe of aedeagus in ventral (c), dorsal (d) and lateral (e) view [0.9 mm]; 10f: sclerite I and dorsal spicule of endophallus [0.6 mm]; 10g: sclerites II–III–IV of endophallus [0.5 mm]; 10h: spermatheca [0.6 mm]; 10k: antenna [2.0 mm]. 11a–b: habitus; 11c: spermatheca [0.4 mm]; 11d: antenna [1.9 mm]. 10a–b: paralectotype (BMNH); 11a–b: paratype (DSPC). scI–IV: sclerites I–IV of endophallus; ds: dorsal spicule. Square brackets: length of scale segment.
FIGURES 18–26. Distribution maps for Metallactus hamifer species-group. M in Revision of the Metallactus hamifer species-group (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 18–26. Distribution maps for Metallactus hamifer species-group. M. abditus (18); M. agonista (19); M. albivittis (20); M. albopictus (21); M. bivitticollis (22); M. chamorroi (23); M. crassicollis (24); M. dicaprioi (25); M. hamifer (26). Grey squares: localities reported in a generic way.
FIGURES 5–6. M in Revision of the Metallactus hamifer species-group (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 5–6. M. bivitticollis (5), M. chamorroi (6). 5a–b: habitus; 5c–e: median lobe of aedeagus in ventral (c), dorsal (d) and lateral (e) view [0.8 mm]; 5f: antenna (apical antennomeres missing) [1.8 mm]; 5g: spermatheca [0.5 mm]. 6a–b: habitus; 6c–e: median lobe of aedeagus in ventral (c), dorsal (d) and lateral (e) view [0.8 mm]; 6f: antenna (apical antennomeres missing) [2.0 mm]; 6g: sclerites of endophallus [0.6 mm]; 6h: spermatheca [0.7 mm]. 5a–b: lectotype; 6a–b: holotype. hd: hairy dent; scI–IV: sclerites I–IV of endophallus. Square brackets: length of scale segment.
FIGURES 7–8. M in Revision of the Metallactus hamifer species-group (Coleoptera: Chrysomelidae: Cryptocephalinae)
FIGURES 7–8. M. crassicollis (7), M. dicaprioi (8). 7a–b: habitus; 7c–e: median lobe of aedeagus in ventral (c), dorsal (d) and lateral (e) view [0.7 mm]; 7f: antenna [2.1 mm]; 7g: sclerites of endophallus [0.2 mm]. 8a–b: habitus; 8c–e: median lobe of aedeagus in ventral (c), dorsal (d) and lateral (e) view [0.7 mm]; 8f: antenna [2.1 mm]; 8g: sclerites I–II and dorsal spicule of endophallus [0.7 mm]; 8h: sclerites III–IV of endophallus [0.5 mm]; 8k: spermatheca [0.5 mm]. 7a–b: paralectotype; 8a–b: holotype. scI–IV: sclerites I–IV of endophallus; ds: dorsal spicule. Square brackets: length of scale segment.
Supplementary material 1 from: Pourmoghaddam MJ, Lambert C, Surup F, Khodaparast SA, Krisai-Greilhuber I, Voglmayr H, Stadler M (2020) Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon spp. against the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture. MycoKeys 66: 105-133. https://doi.org/10.3897/mycokeys.66.50946
Discovery of a new species of the Hypoxylon rubiginosum complex from Iran and antagonistic activities of Hypoxylon species towards the Ash Dieback pathogen, Hymenoscyphus fraxineus, in dual culture
FIGURE 3. A–M, except J in The millipede family Polyxenidae (Diplopoda, Polyxenida) in the faunas of the Crimean Peninsula and Caucasus, with notes on other European Polyxenidae
FIGURE 3. A–M, except J: Propolyxenus argentifer (Verhoeff, 1921) comb. n. Topotype, adult male. A. Head; B. Collum; Tergites showing pattern of trichome insertions: C. Tergite 2, D. Tergite 4; E. Tergite 10; F. Pattern of insertions of dorso-medial fan of trichomes on telson; G. right gnathochilarium; H. Left antenna showing proportions of articles; I. Article VII sensilla; K. Article VI sensilla; L. leg 8; M. Hooked caudal trichome. J. P. argentifer adult male, Russia, Utrish Nature Reserve, Article VII sensilla. Scale bars: A–E = 200 µm; F, G, M = 50 µm; I, J, K = 10 µm; H, L = 100 µm.
Supplementary material 3 from: Grunewald K, Schweppe-Kraft B, Syrbe R-U, Meier S, Krüger T, Schorcht M, Walz U (2020) Hierarchical classification system of Germany's ecosystems as basis for an ecosystem accounting – methods and first results. One Ecosystem 5: e50648. https://doi.org/10.3897/oneeco.5.e50648
The area and share of main ecosystem types and sub ecosystem types (ETs, see Tab. 1)) in the German land cover model (LBM-DE) for the time periods 2012, 2015 and 2018. Linear elements such as small scale structures and infrastructures from the topographic-cartographic Information system (ATKIS) were added to the land cover model.
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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)
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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.
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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.