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1,188 results for “Deltas”
Fig. 1 in Trigonopeltastes delta (Coleoptera: Scarabaeidae: Cetoniinae) Larva Developing in a Bromeliad Terrarium
Fig. 1. Developmental stages of Mylabris phalerata. A: Egg (2.4 mm); B: L1 (2.6 mm); C: L2 (5.1 mm); D: L3 (13.7 mm); E: L4 (22.4 mm); F: L5 (29.2 mm); G: Pupa (30.1 mm); H: Adult (31.2 mm).
Tutorial: Die Rolling Delta Funktion in Stylo nutzen, um Autorenstil zu analysieren
<p>In der Videoreihe „Stilometrie und digitale Literaturanalyse“ erklären wir, wie Stylo für die Stilometrie genutzt wird. Dafür zeigen wir dir, wie du RStudio als Benutzerumgebung für das Tool einrichtest und das Stylo-Package lädst, wie du eigene Korpora zur Analyse vorbereitest und welche Parameter Du dafür festlegen kannst. Außerdem stellen wir verschiedene Arten der Stilanalyse vor und erklären dir die essentiellen Funktionen der grafischen Benutzeroberfläche.<br>In diesem Video zeigen wir die Rolling-Delta-Funktion des Stilometrie-Tools Stylo. Wir erklären, wie Korpora für diese Analyse aufbereitet werden müssen, welche Parameter du festlegen solltest und wie du die Ergebnisse interpretieren kannst.</p> <p> </p> <div> <p>Mehr Infos:</p> <ul> <li>Schriftliche Einführung in die Methodik der Stilometrie: <a href="https://fortext.net/routinen/methoden/stilometrie">https://fortext.net/routinen/methoden/stilometrie</a></li> <li>Schriftliche Lerneinheit zur Stilometrie: <a href="https://fortext.net/routinen/lerneinheiten/stilometrie-mit-stylo">https://fortext.net/routinen/lerneinheiten/stilometrie-mit-stylo</a></li> <li>Link zum Download von R Studio: <a href="https://posit.co/download/rstudio-desktop/">https://posit.co/download/rstudio-desktop/</a></li> <li>Mehr über Stylo und aktuelle Forschung aus der Stilometrie unter: <a href="https://computationalstylistics.github.io/">https://computationalstylistics.github.io/</a></li> </ul> <p> </p> <p>Übersicht der Videoreihe auf Zenodo:</p> <ol> <li><a href="../records/10372243">Tutorial: Stylo installieren</a></li> <li><a href="../records/10372249">Tutorial: Stylo zur Analyse des Autoren-Stils nutzen</a> </li> <li><a href="../records/10371113">Tutorial: Die Rolling Delta Funktion in Stylo nutzen, um Autorenstil zu analysieren</a></li> <li>Fallbeispiel: <a href="../records/10474049">Christoph Martin Wieland und Sophie von la Roche: Eine Dichterfreundschaft mit literarischen Folgen?</a></li> </ol> <p> </p> <p><a href="https://www.youtube.com/watch?v=hp3MTGA_W8o&list=PLu-M0KuYw64oLYDQl7JeGkFxqwe4EcNjY">Hier</a> zur Videoreihe auf Youtube</p> </div>
Data and software for article: "Lava delta formation: Mathematical modelling and laboratory experiments"
<p>Experimental and numerical data and scripts required to reproduce the results of Taylor-West, Balmforth, & Hogg 2024 "Lava delta formation: Mathematical modelling and laboratory experiments". Accepted to JGR: Earth Surfaces. doi:10.1029/2023JF007505</p>
Trajectories of all MD simulations performed of Spike RBD/hACE2 complexes (WT, Delta, BA.1 to BA.4)
<p>Trajectories (.dcd) of the molecular dynamics simulations performed on Spike RBD / hACE2 complexes</p> <p>Protein structure files (.psf) prepared with Charmm36m topology / parameters</p> <p>For the WT (SARS-CoV-2 original strain), 6 additional replicas were uploaded, 3 including all glycans present on both spike and hACE2 et 3 replicas without glycan as control simulations.</p> <p> </p>
Elevation projections for the Mekong delta (Vietnam) under sedimentation strategies, subsidence, compaction, and sea-level rise
<p>Modelled elevation projections for the Mekong delta (Vietnam) to 2050 under scenarios of fluvial sedimentation, organic accumulation, anthropogenic-accelerated subsidence, natural compaction, and global sea-level rise. Data is in meters above sea level and georeferenced (WGS84 UTM zone 48N).<br> For methodology and detailed description of the data, please see Dunn and Minderhoud (2021) DOI to follow, in which part of the dataset is presented in Figure 6.</p>
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
Raw data files for "Dialectical characteristics of morphologies of the delta unit driven by water inflow"
<p>The following dataset is a collection of analytical data of a limited repetition of lab-scale delta evolution for evaluating the dialectical characteristics of delta morphology.</p>
The eclipsing binary systems with delta Scuti component. AB Cas
<p>A set of inlists for MESA v12115, used to compute a grid of binary evolutionary tracks used in the paper "The eclipsing binary systems with delta Scuti component. AB Cas".</p>
FIGURE 3 in Two new earthworm species (Annelida, Oligochaeta, Megascolecidae) from the Mekong delta, Vietnam
FIGURE 3. Metaphire giengensis sp. nov., Holotype (CTU-EW.017.h01). A1 & A2. Ventral view of the male region. B. Dorsal view of testis sacs and seminal vesicles. C1 & C2. Right spermatheca. D. Ventral view of the spermathecal region. E1 & E2. Intestinal caecum; F1 & F2. Right prostate gland. G. Male pore region transverse body section (Non-type: CTU- EW.017.03). H. Body wall transverse section. Scale bar = 1 mm.
FIGURE 1 in Two new earthworm species (Annelida, Oligochaeta, Megascolecidae) from the Mekong delta, Vietnam
FIGURE 1. Collecting sites in Mekong Delta, Vietnam. A. map of Vietnam and relevant provinces (B. An Giang Province. C. Ben Tre Province). Triangle: Metaphire giengensis sp. nov. Circle: Amynthas reductus sp. nov.
Nipponaclerda biwakoensis infestation of Phragmites australis in the Mississippi River Delta, USA: Do fungal microbiomes play a role?
<p>Recently, significant die-back of nonnative common reed, <i>Phragmites australis,</i> has been reported in the Mississippi River Delta (MRD), Louisiana, USA. This dieback has been attributed to an invasive scale insect, <i>Nipponaclerda biwakoensis</i>. We test whether fungi are involved in the recent infestation by this insect and subsequent die-offs of <i>Phragmites australis</i>. Several haplotypes of <i>P. australis</i> occur in the MRD, and the European (M) and Delta (M1) haplotypes appear to experience differing levels of <i>N. biwakoensis </i>infestation. We tested whether these haplotypes differed in their fungal microbiomes in both their leaf and stem tissues, and whether differences in fungal community composition were linked to the level of infestation using a metabarcoding Internal Transcribed Spacer (ITS) amplicon sequencing approach. Our analyses showed differences in fungal community composition and diversity between haplotypes and tissue types, but none of these differences were directly correlated with <i>N. biwakoensis</i> infestation severity. However, we did find that the European haplotype hosted higher putative pathogen loads in stem tissues compared to the Delta haplotype, which may confer resistance to herbivory, though it is possible that differences in infestation between haplotypes are due to morphology.</p>
Neutralizing immunity in vaccine breakthrough infections from the SARS-CoV-2 Omicron and Delta variants
<p>Scripts and metadata used in the analysis of the manuscript, <em>Neutralizing immunity in vaccine breakthrough infections from the SARS-CoV-2 Omicron and Delta variants.</em></p>
Data for 'Multi-modal microscopy imaging with the OpenFlexure Delta Stage'
<p>Image data for 'Multi-modal microscopy imaging with the OpenFlexure Delta Stage'</p>
Distribution. Botswana, in Okavango Delta along Gomoti River, Zambia in Kafue National Park, and Zimbabwe in Mana Pools National Park; it may occur in Mozambique and South Africa. in Vespertilionidae
Distribution. Botswana, in Okavango Delta along Gomoti River, Zambia in Kafue National Park, and Zimbabwe in Mana Pools National Park; it may occur in Mozambique and South Africa.
On following pages: 26. Common Dwarf Bonneted Bat (Eumops bonariensis); 27. Chimera's Bonneted Bat (Eumops 30. Delta Bonneted Bat (Eumops delticus); 31. Fierce Bonneted Bat (Eumops ferox); 32. Florida Bonneted Bat (Eumops hansae); 35. Guianan Bonneted Bat (Eumops maurus); 36. Northern Dwarf Bonneted Bat (Eumops nanus); 37. Patagonian 39. Trumbull's Bonneted Bat (Eumops trumbull)); 40. Underwood's Bonneted Bat (Eumops underwoodi); 41. Wilson's chimaera); 28. Chiribaya's Bonneted Bat (Eumops chiribaya); 29. Big Bonneted Bat (Eumops dabbenei); floridanus); 33. Wagner's Bonneted Bat (Eumops glaucinus); 34. Sanborn's Bonneted Bat (Eumops Dwarf Bonneted Bat (Eumops patagonicus); 38. Western Bonneted Bat (Eumops perotis), Bonneted Bat (Eumops wilsoni). in Molossidae
On following pages: 26. Common Dwarf Bonneted Bat (Eumops bonariensis); 27. Chimera's Bonneted Bat (Eumops 30. Delta Bonneted Bat (Eumops delticus); 31. Fierce Bonneted Bat (Eumops ferox); 32. Florida Bonneted Bat (Eumops hansae); 35. Guianan Bonneted Bat (Eumops maurus); 36. Northern Dwarf Bonneted Bat (Eumops nanus); 37. Patagonian 39. Trumbull's Bonneted Bat (Eumops trumbull)); 40. Underwood's Bonneted Bat (Eumops underwoodi); 41. Wilson's chimaera); 28. Chiribaya's Bonneted Bat (Eumops chiribaya); 29. Big Bonneted Bat (Eumops dabbenei); floridanus); 33. Wagner's Bonneted Bat (Eumops glaucinus); 34. Sanborn's Bonneted Bat (Eumops Dwarf Bonneted Bat (Eumops patagonicus); 38. Western Bonneted Bat (Eumops perotis), Bonneted Bat (Eumops wilsoni).
Distribution. North America, from the Mackenzie River Delta, Northwest Territories, Canada, S throughout Canada and USA, excluding peninsular Florida and arid parts of the SW, to N Mexico (Baja California to Tamaulipas). North American Beavers have been introduced into Europe (Finland, Russia, Central Europe), Russian Far East (Kamchatka and Sakhalin Island), and Tierra del Fuego, Argentina. in Castoridae
Distribution. North America, from the Mackenzie River Delta, Northwest Territories, Canada, S throughout Canada and USA, excluding peninsular Florida and arid parts of the SW, to N Mexico (Baja California to Tamaulipas). North American Beavers have been introduced into Europe (Finland, Russia, Central Europe), Russian Far East (Kamchatka and Sakhalin Island), and Tierra del Fuego, Argentina.
Distribution. Coastal areas and large inland rivers of West Africa from the Senegal River at the Mauritania—Senegal border S to the Longa River in Angola. They occur as far as 2000 km from the ocean in the Inner Niger Delta of Mali, up to 75 km off the continental shore in the shallows and mangrove creeks of the Bijagos Archipelago of Guinea-Bissau, and as far E as Lake Tréné in Chad; formerly in Lake Chad itself. in Trichechidae
Distribution. Coastal areas and large inland rivers of West Africa from the Senegal River at the Mauritania—Senegal border S to the Longa River in Angola. They occur as far as 2000 km from the ocean in the Inner Niger Delta of Mali, up to 75 km off the continental shore in the shallows and mangrove creeks of the Bijagos Archipelago of Guinea-Bissau, and as far E as Lake Tréné in Chad; formerly in Lake Chad itself.
Distribution. NE & S Venezuela (Orinoco Delta and S of the Orinoco River), the Guianas, N & NC Brazil (along the Amazon River W to Maranhao and S to Para and Mato Grosso states), and into upper Amazon Basin of SW Colombia (N up to Meta and Guainia departments), E Ecuador, and NE & E Peru; its S limit in W Amazonian Brazil is unclear. Additional visual records are described for SE Para State and need to be confirmed. in Megalonychidae
Distribution. NE & S Venezuela (Orinoco Delta and S of the Orinoco River), the Guianas, N & NC Brazil (along the Amazon River W to Maranhao and S to Para and Mato Grosso states), and into upper Amazon Basin of SW Colombia (N up to Meta and Guainia departments), E Ecuador, and NE & E Peru; its S limit in W Amazonian Brazil is unclear. Additional visual records are described for SE Para State and need to be confirmed.
On following pages: 60. Orinoco Four-eyed Opossum (Philander deltae); 61. Mcllhenny's Foureyed Opossum (Philander mcilhennyi); 62. Mondolfi's Foureyed Opossum (Philander mondolfii); 63. Olrog's Four-eyed Opossum in Didelphidae
On following pages: 60. Orinoco Four-eyed Opossum (Philander deltae); 61. Mcllhenny's Foureyed Opossum (Philander mcilhennyi); 62. Mondolfi's Foureyed Opossum (Philander mondolfii); 63. Olrog's Four-eyed Opossum
On following pages: 60. Orinoco Four-eyed Opossum (Philander deltae); 61. Mcllhenny's Foureyed Opossum (Philander mcilhennyi); 62. Mondolfi's Foureyed Opossum (Philander mondolfii); 63. Olrog's Four-eyed Opossum (Philander olrogi); 64. Gray Four-eyed Opossum (Philander opossum). in Didelphidae
On following pages: 60. Orinoco Four-eyed Opossum (Philander deltae); 61. Mcllhenny's Foureyed Opossum (Philander mcilhennyi); 62. Mondolfi's Foureyed Opossum (Philander mondolfii); 63. Olrog's Four-eyed Opossum (Philander olrogi); 64. Gray Four-eyed Opossum (Philander opossum).
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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.