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INTAROS CTD mooring data from Young Sound, NE Greenland (2018-2021)
<p>Greenland fjords are currently undergoing significant ecosystem change due to unprecedented melting of the Greenland Ice Sheet (GrIS).The rapidly increasing discharge of GrIS meltwater not only influences circulation patterns and stratification of the water column, but it also introduces large fluxes of inorganic sediments and organic material that are suspended in the water column. These inputs can limit light availability to primary producers. However, data is still limited for most Greenland fjord systems and there is an especial paucity of data showing yearly cycles. The Integrated Arctic Observation System (INTAROS) project funded by the European Commission’s H2020 programme allowed for the deployment of two moorings equipped with CTDs in the Young Sound fjord system––one in the inner fjord closest to GrIS meltwater discharge and another in the outer fjord region. This dataset reports the temperature and salinity recorded on these two moorings over 3 yearly cycles from August 2018 to August 2021. The moored CTDs were RBR Maestro<sup>3</sup> and Concerto<sup>3</sup> and were deployed at ~10 and ~20m in the inner and outer fjord respectively. Data were recorded at 2 Hz with measurements taken at 5min–1h intervals and raw data were processed using RBR Ruskin software. This dataset is made up of comma separated CSV files separated by mooring and year.</p> <p>We would like to thank Carl Isaksen and MarineBasis, Greenland Ecosystem Monitoring Programme (<a href="https://g-e-m.dk/">https://g-e-m.dk</a>) for assistance during deployment. The moorings were funded by the EU Horizon2020 funded project INTAROS (grant no. 727890). </p>
Supplementary material 1 from: Pontoppidan M, Nachman G (2013) Spatial Amphibian Impact Assessment – a management tool for assessment of road effects on regional populations of Moor frogs (Rana arvalis). Nature Conservation 5: 29-52. https://doi.org/10.3897/natureconservation.5.4612
Full model description following the protocol suggested by Grimm et al. (2006, 2010) and model parameterisation. (doi: 10.3897/natureconservation.5.4612.app). File format: Adobe PDF document (pdf).:
FIGURE 18. Septopora blanda Moore, 1929 in Stenolaemate bryozoans from the Graham Formation, Pennsylvanian (Virgilian) at Lost Creek Lake, Texas, USA
FIGURE 18. Septopora blanda Moore, 1929 (A–C): A, B – tangential section showing autozooecial apertures and chambers, and cyclozooecia (arrows) (XCI 47); C – tangential section showing autozooecial chambers and cyclozooecia (XCI 54). Penniretepora flexistriata Richards, 1959 (D–J): D–F – colony fragments with autozooecial apertures with apertural pores (arrows) and stellate structures, divided by low undulating keel (D: (XCI 121), E–F: (XCI 122); G – autozooecial aperture with apertural pore (arrow) and stellate structure (XCI 123); H, I – thin section showing autozooecial chambers (XCI 83); J – thin section showing autozooecial apertures with apertural pore (arrow) (XCI 82).
FIGURE 11. Laxifenestella placida Moore, 1929 in Stenolaemate bryozoans from the Graham Formation, Pennsylvanian (Virgilian) at Lost Creek Lake, Texas, USA
FIGURE 11. Laxifenestella placida Moore, 1929 (A–D): A – tangential section showing autozooecial apertures and keel with nodes (XCI 35); B – deep tangential section showing autozooecial chambers with hemisepta (XCI 65); C, D – colony fragment showing fenestrules, autozooecial apertures and keels with nodes (XCI 108). Laxifenestella texana n. sp. (E, F) – tangential section showing fenestrules, autozooecial apertures and chambers, keels with nodes, and reproductive heterozooecia (arrows), holotype (XCI 81).
FIGURE 6. Cystodictya formosa Moore, 1929 in Stenolaemate bryozoans from the Graham Formation, Pennsylvanian (Virgilian) at Lost Creek Lake, Texas, USA
FIGURE 6. Cystodictya formosa Moore, 1929 (A–B): A – deep tangential section showing autozooecial chambers with hemisepta and vesicular skeleton (XCI 27); B – branch transverse section showing mesotheca, autozooecial chambers and vesicles (XCI 23c). Goniocladia grahamensis Moore, 1929 (C–E): branch fragment showing the shape of fenestrule, ridges on branches and autozooecial apertures with lunaria (XCI 100). Dyscritella felixi n. sp. (F–H): F – colony encrusting a brachiopod spine (holotype XCI 101); G – colony surface showing autozooecial apertures, exilazooecia, and acanthostyles; H – tangential thin section showing autozooecial apertures, exilazooecia, and acanthostyles (paratype XCI 86).
FIGURE 17. Polypora aff. hexagona Moore, 1929 in Stenolaemate bryozoans from the Graham Formation, Pennsylvanian (Virgilian) at Lost Creek Lake, Texas, USA
FIGURE 17. Polypora aff. hexagona Moore, 1929 (A–E): tangential section showing autozooecial apertures and chambers, nodes, microstyles, and reproductive heterozooecia (arrows) (XCI 55). Septopora blanda Moore, 1929 (F– I): F – tangential section showing autozooecial chambers and cyclozooecia (XCI 54); G – colony fragment with cyclozooecia on the reverse side (arrows) (XCI 119). H, I – colony fragment with autozooecial apertures, keel nodes, and cyclozooecia (arrows) (XCI 120).
FIGURE 19. Penniretepora oculata Moore, 1929 in Stenolaemate bryozoans from the Graham Formation, Pennsylvanian (Virgilian) at Lost Creek Lake, Texas, USA
FIGURE 19. Penniretepora oculata Moore, 1929 (A–E): A, B – branch fragment with autozooecial apertures divided by keel with nodes (XCI 124); C, D – tangential section showing autozooecial chambers (XCI 96); E – tangential section showing autozooecial apertures (arrow: nanozooecium) (XCI 96).
FIGURE 6. Macrobdella ditetra Moore, 1953 in Range Extension for the Elusive New England Medicinal Leech, Macrobdella sestertia Whitman, 1886 (Hirudinida: Macrobdellidae), in South Carolina, U.S.A., with Notes on Morphology, Coloration, and Biology
FIGURE 6. Macrobdella ditetra Moore, 1953 (CASIZ 224103) feeding on Lithobates sphenocephalus (Cope, 1886); arrows point to the leech.
Figs 12–13. Ethmia lineatonotella MOORE, 1867 in A Review Of The Ethmia Lineatonotella Species Group, With Description Of Two New Species (Lepidoptera, Ethmiidae)
Figs 12–13. Ethmia lineatonotella MOORE, 1867, genitalia: 12 = male, KUN Gen. No. 263, 13 = female, KUN Gen. No. 251
Figs. 1–5 in Two new species of genus Zadadra Moore (Lepidoptera: Erebidae: Arctiinae) from India
Figs. 1–5. Zadadra cucullata sp. nov. 1, Adult male. 2, Male genitalia. 3, Uncus with Tegumen. 4, Valva. 5, Aedeagus.
Figs. 1-7 in A new species of the genus Ditrigona Moore, 1888 (Lepidoptera: Drepanidae) in China
Figs. 1-7. Ditrigona clavata sp. nov. 1. Male, holotype; 2. Female, Paratype. 3. Male genitalia; 4. Aedeagus; 5. 8th tergite; 6. 8th sternite; 7. Female genitalia.
Рис. 1. Cyana guttifera (Walker, 1856) (A — самец, B — самка), Cyana adita (Moore, 1859) (C, D — самцы) и Cyana puella (Drury, 1773) (E — самец, F — самка) из Пакистана. Масштабная Λинейка = 5 мм Fig. 1. Cyana guttifera (Walker, 1856) (A — male, B — female), Cyana adita (Moore, 1859) (C, D — males) and Cyana puella (Drury, 1773) (E — male, F — female) from Pakistan. Scale bar = 5 mm in New records of Cyana Walker, 1854 from Pakistan (Lepidoptera: Erebiae: Arctiinae)
Рис. 1. Cyana guttifera (Walker, 1856) (A — самец, B — самка), Cyana adita (Moore, 1859) (C, D — самцы) и Cyana puella (Drury, 1773) (E — самец, F — самка) из Пакистана. Масштабная Λинейка = 5 мм Fig. 1. Cyana guttifera (Walker, 1856) (A — male, B — female), Cyana adita (Moore, 1859) (C, D — males) and Cyana puella (Drury, 1773) (E — male, F — female) from Pakistan. Scale bar = 5 mm
Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) in Call repertoire of Bitterns Ixobrychus in Russian Far East
Рис. 1. Брачные крики и их инΑивиΑуаΛьная изменчивость у разных виΑов воΛчков: a — I. m. minutes (Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016) Fig. 1. Mating calls and their individual variability in different bittern species: a — I. m.minutes Celmins 2008; Bruggen 2017; Maffezzoli 2021); b — I. m. dubius (Graff 2012; Davison 2020); c — I. m. payesii (Hesse 2009; Archer 2019; Cockcroft 2020); d — I. sinensis (Piot 2021; Raveendran 2021; Jeff 2022); e — I. e. exilis (Graves 2021; Overholtz 2021); f — I. e. peruvianus (Moore 2003; Krabbe 2015; Arias 2020); g — I. eurythmus (Mark 1997; Lastukhin 2015; Wulf 2016)
Water temperature mooring (M1-M20) data along the central California inner shelf
<p>Water emperature Mooring Data M1-M1 (ten minute averages)</p> <p>The data were collected as part of the Office of Naval Research Inner Shelf DRI in the Fall of 2017</p> <p>The data are used in the manuscript entitled</p> <p>"Statistical analysis of vertical and alongshore temperature variability in the subtidal, diurnal, and semidiurnal frequency bands along the central California inner shelf"</p> <p>by </p> <p>Jamie H. MacMahan, Falk Feddersen, Thomas M. Freismuth, Matt K. Gough, and Michael Kovatch</p> <p> </p>
H2020 OPERA Project: Mooring System Experimental data from MARMOK-A-5 Wave Energy Converter at BiMEP
<p>Funded under European Union's Horizon 2020 Programme, <a href="http://opera-h2020.eu/">OPERA</a> project’s main objective is to reduce the time to market of wave energy, by further advancing in 4 key innovations aiming to reduce up to 50% the Levelized Cost of Energy (LCOE) projections of a floating Oscillating Water Column (OWC) technology.</p> <p>As part of project activities, a condition monitoring system was deployed during the open-sea testing campaign of IDOM's MARMOK-A-5 wave energy converter, while this was deployed in the Biscay Marine Energy Platform (BiMEP) from October 2016 to June 2019.</p> <p>The dataset herein contains a collection of experimental results obtained during this extensive testing campaign, The campaign covers two deployment periods, where the first testing period includes polyesther tethers and the second testing campaing includes innovative elastomeric tethers as described in more detail in the project documentation. This experimental dataset aims to provide quantitative comparison data of the dynamic behavior of the system under these two different configurations.</p>
Figures 1-6. 1. Abisara bifasciata Moore, 1877. 2. Pareronia hippia Fabricius, 1787. 3. Elymnias hypermnestra Linnaeus, 1763. 4&5. Acraea terpsicore Linnaeus, 1758. 6. Charaxes solon Fabricius, 1793 in New records of butterflies (Lepidoptera: Insecta) from Jammu and Kashmir Himalaya
Figures 1-6. 1. Abisara bifasciata Moore, 1877. 2. Pareronia hippia Fabricius, 1787. 3. Elymnias hypermnestra Linnaeus, 1763. 4&5. Acraea terpsicore Linnaeus, 1758. 6. Charaxes solon Fabricius, 1793.
Figures 7-12. Symphaedra nais Forster, 1771 9. Neptis jumbah Moore, 1858. 10. Moduza procris Cramer, 1777. 11. Athyma cama Moore, 1857. 12. Tajuria jehana Moore, 1884 in New records of butterflies (Lepidoptera: Insecta) from Jammu and Kashmir Himalaya
Figures 7-12. Symphaedra nais Forster, 1771 9. Neptis jumbah Moore, 1858. 10. Moduza procris Cramer, 1777. 11. Athyma cama Moore, 1857. 12. Tajuria jehana Moore, 1884.
Figures 8–18 in Two New records of the genus Padenia Moore, 1882 (Lepidoptera: Erebidae: Arctiinae: Lithosiini) from India
Figures 8–18. Padenia spp.. adults.. Male & female genitalia; 8, 9 & 10. P. transversa; 11, 12 & 13. P. acutifascia; 14, 15 & 16. P. obliquifascia; 17 & 18. P. duplicana.
Figures 1–7 in Two New records of the genus Padenia Moore, 1882 (Lepidoptera: Erebidae: Arctiinae: Lithosiini) from India
Figures 1–7. Padenia spp.. adults 1. P. transversa♂; 2. P. transversa♀; 3. P. acutifascia♂; 4. P. acutifascia♀; 5. P. obiliquifascia♂; 6. P. obilquifascia ♀; 7. P. duplicana ♂ give.
Figure 2 in A new combination of a tussock moth species under Genus Himala Moore (Lepidoptera: Erebidae: Lymantriinae) and its range extension
Figure 2. AdultHimala ochripes (Moore) comb. n.: 1. Forewing, 2. Hindwing, 3. Male Genitalia – ventral view, 4. Dorsal view of male genitalia, 5. Lateral view of male genitalia, 6. Valva, 7. Aedeagus.
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Allen Brain Atlas
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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.
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.