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26 results for “Presence records”
Vulnerable Marine Ecosystem Indicator Taxa recorded by submarine as evidence of the presence of Vulnerable Marine Ecosystems, Antarctic Peninsula - images
<p>This resource contains images that are framegrabs from video recorded by submarine deployed by the MY Arctic Sunrise during their Antarctica expeditions. The first took place in 2018 and focused within the Gerlache Strait and along the western Antarctic Peninsula and the Antarctic Sound in January 2018. Dives were conducted beginning 19th to 27th January 2018. This resource supplement the images for “Vulnerable Marine Ecosystem Indicator Taxa recorded by submarine as evidence of the presence of Vulnerable Marine Ecosystems, Antarctic Peninsula - data”</p>
Data for Marine Ecological Niche Models, for 2019 and across RCP 2.6, 4.5, and 8.5 scenarios in 2050 and 2100: Global-scale Environmental parameters at 0.1° and 0.5° resolutions, Presence and Absence Records of 1508 European-seas Species
<p>Data for Ecological Niche Models: Global-scale Environmental parameters at 0.1° and 0.5° resolutions, Presence and Absence Records of 1508 European-seas Species.</p>
Fig. 1 - A in Short Communications First record of the presence and reproduction of the two-tailed pasha Charaxes jasius (Linnaeus 1767) (Lepidoptera: Nymphalidae) in northeastern Italy
Fig. 1 - A male observed in the xerothermic oasis of Monte Ceva on 7 September 2021. / Un maschio osservato nell'oasi xerotermica del Monte Ceva il 7 Settembre 2021.
"It was recorded on Sunday, morning of the 28th of September as some of the slower runners of the Berlin Marathon made it past Torstrasse near my flat. Iwas out to buy some bread for breakfast, but Iusually bring a camera and my Edirol R-1 recorder whenever Igo out. Since Iwas freshly returned to Berlin Iguess Iwas sensitive to the more antiquated sounds which still survive there, like that of the organ grinder. Iam generally interested in how human beings are replacing the presence of Nature with an artificial environment made entirely by human hands (and thus far more understandable, it is hoped). In this new Human Nature, the sounds of Nature are also Human made. Iwrite about these things, but Ialso use the sounds in my videos and my interactive and generative media work, so generally Iam wandering around building up my archive of media documents for use as material in future works." [Baruch/ gottlieb]17 in Collecting Sounds. Online Sharing of Field Recordings as Cultural Practice
"It was recorded on Sunday, morning of the 28th of September as some of the slower runners of the Berlin Marathon made it past Torstrasse near my flat. Iwas out to buy some bread for breakfast, but Iusually bring a camera and my Edirol R-1 recorder whenever Igo out. Since Iwas freshly returned to Berlin Iguess Iwas sensitive to the more antiquated sounds which still survive there, like that of the organ grinder. Iam generally interested in how human beings are replacing the presence of Nature with an artificial environment made entirely by human hands (and thus far more understandable, it is hoped). In this new Human Nature, the sounds of Nature are also Human made. Iwrite about these things, but Ialso use the sounds in my videos and my interactive and generative media work, so generally Iam wandering around building up my archive of media documents for use as material in future works." [Baruch/ gottlieb]17
Distribution. Pakistan, India, Sri Lanka, and Nepal to China, Mainland SE Asia, Peninsular Malaysia, Sumatra, Java, Borneo, the Philippines, and many ssa small islands. Also scattered records in Sulawesi, Moluccan Is, Timor, and the Aru Is, probably resulting from introductions. Presence uncertain in Papua New Guinea. Introduced to Japan in the late 1800s. in Viverridae
Distribution. Pakistan, India, Sri Lanka, and Nepal to China, Mainland SE Asia, Peninsular Malaysia, Sumatra, Java, Borneo, the Philippines, and many ssa small islands. Also scattered records in Sulawesi, Moluccan Is, Timor, and the Aru Is, probably resulting from introductions. Presence uncertain in Papua New Guinea. Introduced to Japan in the late 1800s.
Distribution. Main tropical rainforest belt from Senegal and Guinea Bissau to NW Uganda and E DR Congo, reaching as S boundary N Angola (Cabinda); no recent records from Gambia or Chad and its presence is uncertain in S Sudan and SW Ethiopia. As a species that may range widely through gallery forests, it may also occur in adjacent countries. in Suidae
Distribution. Main tropical rainforest belt from Senegal and Guinea Bissau to NW Uganda and E DR Congo, reaching as S boundary N Angola (Cabinda); no recent records from Gambia or Chad and its presence is uncertain in S Sudan and SW Ethiopia. As a species that may range widely through gallery forests, it may also occur in adjacent countries.
Distribution. New Caledonia (Grande Terre), with acoustic records across much of the island; also one from the nearby Loyalty Is (Lifou), but presence there needs confirmation. in Vespertilionidae
Distribution. New Caledonia (Grande Terre), with acoustic records across much of the island; also one from the nearby Loyalty Is (Lifou), but presence there needs confirmation.
Distribution. India, Sri Lanka, Myanmar, China, Thailand, Laos, Vietham, Cambodia, Borneo, Java, Lesser Sunda Is (Bali and Lombok), and Philippines; presence in Bangladesh is very likely but needs confirmation. Previous records on Malay Peninsula and Sumatra need further verification as to whether the populations may have disappeared or may have been misidentified. in Molossidae
Distribution. India, Sri Lanka, Myanmar, China, Thailand, Laos, Vietham, Cambodia, Borneo, Java, Lesser Sunda Is (Bali and Lombok), and Philippines; presence in Bangladesh is very likely but needs confirmation. Previous records on Malay Peninsula and Sumatra need further verification as to whether the populations may have disappeared or may have been misidentified.
Distribution. Disjunct range, recorded in NE India and Bangladesh (Chittagong) and in SE Asia (Thailand, Laos, Vietnam, and Cambodia). Presence in all Myanmar expected, which would connect these areas. in Pteropodidae
Distribution. Disjunct range, recorded in NE India and Bangladesh (Chittagong) and in SE Asia (Thailand, Laos, Vietnam, and Cambodia). Presence in all Myanmar expected, which would connect these areas.
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation. in Cercopithecidae
Distribution. NW DR Congo and NE Republic of the Congo, in lowland forests of the Congo Basin on both sides of the lower and middle Congo (c.16" E to 26°-27° E); S of the Congo Riverits distribution extends E to the Lomami River system (c.3° N to 6° 30° S); it has also been recorded on twoislands in the Sangha River. Its presence in NE Angola requires confirmation.
fig. 1 in First record of Serrapinnus kriegi (Schindler, 1937) and confirmed presence of S. calliurus (Boulenger, 1900) for Uruguay (Characiformes: Characidae)
fig. 1. (above left) Serrapinnus calliurus. Top, male (MHNM 3783), Paso de la Cruz, Cuareim River, Artigas Department, Uruguay. Bottom, female (not preserved), Franquia, Bella Unión, Artigas Department, Uruguay. Specimens alive, upon capture. fig. 2. (above right) Serrapinnus kriegi. Top, male (MHNM 3794), Paso de la Cruz, Cuareim River, Artigas Department, Uruguay. Bottom, female (MHNM 3560), Paso de León, Cuareim River, Artigas Department, Uruguay. Specimens alive, upon capture. fig. 3. (right) Geographic distribution of the genus Serrapinnus in Uruguay. Red dots corresponds to S. calliurus and green dots to sites with both, S. kriegi and S. calliurus.
FIGURE 2 in Confirmation of Acer campestre (Sapindaceae) presence in Algeria and new sites records
FIGURE 2. Acer campestre occurrence map in Algeria. 1: Larbaa. 2: Tamesguida. 3: Lma Bared. 4: Taza forest house. 5: Ghoubia. 6: Road cw137 next to Ghoubia. 7: Oued Taza. 8: Canyon of Taza. 9: Oued dar l'oued. 10: Louta louatine. 11: Road cw137 next to Betacha. 12: Djebel Babor. 13: Djebel Mégriss. 14: Adrar Amellal. 15: Takoucht 16: Kefrida. 17: Djamaa-n'salah. 18: Laarawath. 19: Thaassasth. 20: Issek.
FIGURE 5. a in Confirmation of Acer campestre (Sapindaceae) presence in Algeria and new sites records
FIGURE 5. a. Acer campestre fruit corymbs harvested at Thaassasth (September, 2020). b. Detached samaras. c. Disamaras harvested at Ghoubia (November, 2022). Photographed by Z. Chikhaoui.
FIGURE 1. a in Confirmation of Acer campestre (Sapindaceae) presence in Algeria and new sites records
FIGURE 1. a. General view of Issek Mountain. b–c. Acer campestre gall-infested leaves (June, 2021). Photographed by Z. Chikhaoui.
FIGURE 4. a in Confirmation of Acer campestre (Sapindaceae) presence in Algeria and new sites records
FIGURE 4. a. Acer campestre shoot with three pairs of leaves collected at Taza forest house in November, 2022. b. Leaf blade base. c. Primary and secondary nerves intersection. d. Petiole. Photographed by Z. Chikhaoui.
FIGURE 3. a. Acer campestre young tree bark. b. Aged tree bark. c in Confirmation of Acer campestre (Sapindaceae) presence in Algeria and new sites records
FIGURE 3. a. Acer campestre young tree bark. b. Aged tree bark. c. Shoot of the year. d. Axillary bud. e. Terminal bud. Photographed by S. Ait Said (a–b) and Z. Chikhaoui (c–e).
FIGURE 1 in An unexpected Rhombophryne record at Tsingy de Bemaraha confirms the presence of cophyline frogs in western Madagascar
FIGURE 1. Dorsal and ventral side of preserved specimens belonging to the genus Rhombophryne: (A) Rhombophryne testudo: (MRSN A2494, from Lokobe, Nosy Be, NW Madagascar); (B) Rhombophryne sp. (MRSN A5524, from PN Tsingy de Bemaraha, W Madagascar); (C) Rhombophryne coudreaui (MRSN A2496, from Mahalevona, Masoala Peninsula, NE Madagascar).
Figs. 7–8 in Presence of Dichotomius (dichotomius) centralis (Harold) in Mexico and a New State Record for Dichotomius amplicollis (Harold) (Coleoptera: Scarabaeidae: Scarabaeinae)
Figs. 7–8. Known and potential distributions of 7) Dichotomius centralis and 8) Dichotomius amplicollis.
Figs. 1–6. Dichotomius species. D in Presence of Dichotomius (dichotomius) centralis (Harold) in Mexico and a New State Record for Dichotomius amplicollis (Harold) (Coleoptera: Scarabaeidae: Scarabaeinae)
Figs. 1–6. Dichotomius species. D. centralis: 1) Parameres, dorsal view; 2) Paramere, apex; 3) Elytral striae. D. amplicollis: 4) Parameres, dorsal view; 5) Paramere, apex; 6) Elytral striae.
FIGURE 5 in First record of Amorphinopsis atlantica (Porifera: Demospongiae: Halicondriidae) in the Paraguaçu River estuary: Is its presence an invasion or an adaptation to changing environmental conditions?
FIGURE 5. Scanning electron microscopy images of Amorphinopsis atlantica spicules. (A and B) Two oxeas varying in size and curvature. (C) Style. (D) Detail of the tip of the oxea. (E) Detail of the tip of the style. (F) General view of oxeas and styles. Scale bars: A, B = 250 μm; C = 50 μm; D, E = 10 μm; F = 200 μm.
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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.