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137 results for “gulls”
Fig. 1 in Abundance And Seasonal Migration Of Gulls (Laridae) On The Lithuanian Baltic Sea Coast
Fig. 1. Annual intensity dynamics of the Little Gull (Larus minutus) spring migration on the Lithuanian Baltic Sea coast
Fig. 5 in Abundance And Seasonal Migration Of Gulls (Laridae) On The Lithuanian Baltic Sea Coast
Fig. 5. Annual intensity dynamics of the Herring Gull (Larus argentatus) spring migration on the Lithuanian Baltic Sea coast
Рис. 3. РаспреΑеΛение чайковых птиц (А — тихоокеанская чайка, Б — восточносибирская чайка, В — бургомистр, Г — моевка) в Охотском море и сопреΑеΛьных воΑах Тихого океана и Японского моря по резуΛьтатам суΑовых учетов в февраΛе — мае 2020 г. (особей/ км2 на 10-минутных трансектах). СпΛошными Λиниями показаны учетные трансекты, пунктиром — 200-метровая изобата Fig. 3. Distribution of larids — (А) slaty-backed gull, (Б) Vega gull, (В) glaucous gull, (Г) blacklegged kittiwake — in the Sea of Okhotsk and adjacent waters of the Pacific Ocean and the Sea of Japan in February–May 2020 (birds/km2 on 10-minute transects). Solid lines indicate transects, dotted line indicates a 200 m isobath in Population of seabirds in the Sea of Okhotsk and adjacent waters of the Pacific Ocean and the Sea of Japan during the winter-spring period of 2020
Рис. 3. РаспреΑеΛение чайковых птиц (А — тихоокеанская чайка, Б — восточносибирская чайка, В — бургомистр, Г — моевка) в Охотском море и сопреΑеΛьных воΑах Тихого океана и Японского моря по резуΛьтатам суΑовых учетов в февраΛе — мае 2020 г. (особей/ км2 на 10-минутных трансектах). СпΛошными Λиниями показаны учетные трансекты, пунктиром — 200-метровая изобата Fig. 3. Distribution of larids — (А) slaty-backed gull, (Б) Vega gull, (В) glaucous gull, (Г) blacklegged kittiwake — in the Sea of Okhotsk and adjacent waters of the Pacific Ocean and the Sea of Japan in February–May 2020 (birds/km2 on 10-minute transects). Solid lines indicate transects, dotted line indicates a 200 m isobath
Рис. 4. Рисунок на конце правого крыΛа американской чайки с нижней стороны Fig. 4. Right under wingtip pattern of the American herring gull in American herring gull Larus smithsonianus Coues, 1862 is a new species for the avifauna of Russia
Рис. 4. Рисунок на конце правого крыΛа американской чайки с нижней стороны Fig. 4. Right under wingtip pattern of the American herring gull
Рис. 2. Американская чайка (в центре) среΑи Αругих виΑов чаек и гΛупышей Fig. 2. American herring gull (in the center) among other gulls and northern fulmars in American herring gull Larus smithsonianus Coues, 1862 is a new species for the avifauna of Russia
Рис. 2. Американская чайка (в центре) среΑи Αругих виΑов чаек и гΛупышей Fig. 2. American herring gull (in the center) among other gulls and northern fulmars
Рис. 3. Рисунки на концах крыΛьев американской чайки с верхней стороны Fig. 3. Left and right upper wingtip patterns of the American herring gull in American herring gull Larus smithsonianus Coues, 1862 is a new species for the avifauna of Russia
Рис. 3. Рисунки на концах крыΛьев американской чайки с верхней стороны Fig. 3. Left and right upper wingtip patterns of the American herring gull
Рис. 1. Американская чайка, зарегистрированная 25 января 2015 г. у побережья ЮгоЗапаΑной Камчатки в Охотском море Fig. 1. American herring gull recorded on 25.01.2015 off the south-west Kamchatka coast in the Sea of Okhotsk in American herring gull Larus smithsonianus Coues, 1862 is a new species for the avifauna of Russia
Рис. 1. Американская чайка, зарегистрированная 25 января 2015 г. у побережья ЮгоЗапаΑной Камчатки в Охотском море Fig. 1. American herring gull recorded on 25.01.2015 off the south-west Kamchatka coast in the Sea of Okhotsk
Рис. 2. Чайка КумΛиена, зарегистрированная 2 марта 2020 г. в северо-восточной части Охотского моря Fig. 2. Kumlien's gull recorded on 2 March 2020 in the northeast Sea of Okhotsk in The first documented record of the Kumlien's gull Larus glaucoides kumlieni Brewster, 1883 in Russia
Рис. 2. Чайка КумΛиена, зарегистрированная 2 марта 2020 г. в северо-восточной части Охотского моря Fig. 2. Kumlien's gull recorded on 2 March 2020 in the northeast Sea of Okhotsk
Рис. 3. Оценка окраски меΛанином первостепенных маховых P6–P10 чайки КумΛиена (баΛΛы по критерию ИнгоΛфссона) Fig. 3. Primary Pattern Score of Kumlien's gull assessed using the Ingolfsson criteria (1970) in The first documented record of the Kumlien's gull Larus glaucoides kumlieni Brewster, 1883 in Russia
Рис. 3. Оценка окраски меΛанином первостепенных маховых P6–P10 чайки КумΛиена (баΛΛы по критерию ИнгоΛфссона) Fig. 3. Primary Pattern Score of Kumlien's gull assessed using the Ingolfsson criteria (1970)
Рис. 16. Пуховой птенец тихоокеанской чайки Larus schistisagus. ЗаΛив Счастья, остров Чаечный, 14.07.2018. Фото В. В. Пронкевича Fig. 16. Downy chick of the Slaty-backed Gull Larus schistisagus. Bay of Schastꞌе, Chaechny Island, 14.07.2018. Photo by V. V. Pronkevich in New data on rare and insufficiently studied birds of the Shchastya Bay, the Sea of Okhotsk, and adjacent territories (Khabarovsk Krai)
Рис. 16. Пуховой птенец тихоокеанской чайки Larus schistisagus. ЗаΛив Счастья, остров Чаечный, 14.07.2018. Фото В. В. Пронкевича Fig. 16. Downy chick of the Slaty-backed Gull Larus schistisagus. Bay of Schastꞌе, Chaechny Island, 14.07.2018. Photo by V. V. Pronkevich
Fig. 4 in Exposure of yellow-legged gulls to Toxoplasma gondii along the Western Mediterranean coasts: Tales from a sentinel
Fig. 4. Biplots of δ13C and δ15N (a) and δ34S and δ15N (b) representing the isotopic variability of yellow-legged gull albumen samples as a response of their immunological status against T. gondii. Isotopic signatures (as a proxy of females' diet) and egg/nest immunological status (as a proxy of females' exposure to the parasite) does not appear to be related. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Exposure of yellow-legged gulls to Toxoplasma gondii along the Western Mediterranean coasts: Tales from a sentinel
Fig. 3. Location and status of yellow-legged gull nests sampled in 2016 and screened for anti-T.gondii antibodies. Base map: Google©. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Exposure of yellow-legged gulls to Toxoplasma gondii along the Western Mediterranean coasts: Tales from a sentinel
Fig. 2. Limited temporal variations of the prevalence of anti-T. gondii antibody in yellow-legged gull egg yolk samples between 2009 and 2016 in three colonies: Frioul, Gruissan and Medes Islands. Curves correspond to cubic splined fitted to the yearly prevalences for visualisation purposes only. Bars indicate 95% Clopper-Pearson confidence intervals. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Exposure of yellow-legged gulls to Toxoplasma gondii along the Western Mediterranean coasts: Tales from a sentinel
Fig. 1. Map of prevalences of anti-T. gondii antibodies in yellow-legged gull egg yolk samples in 2009 (a) and 2016 (b) illustrating the spatial variability. RIO: Riou; FRI: Frioul; CAR: Carteau; VIC: Vicla-Gardiole; GRU: Gruissan; HOT: Hortel; SID: Sidrière; COR: Corrège; MED: Medes; BCN: Barcelona; EBR: Ebro Delta; DRA: Dragonera; AIR: Illa de l'Aire; SSF: Sfax; HDJ: Djerba. Coloured circles highlight the colonies in which temporal variations were explored (Fig. 2).Sample sizes and confidence intervals are given in Appendix A, Table S1.1. Base map: esri ©. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Figure 8. Aploparaksis xemae Schiller, 1951 in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 8. Aploparaksis xemae Schiller, 1951. Type-specimen from Xema sabini, Alaska: (A) hooks, (B) hermaphroditic proglottis, (C) cirrus. Specimen from a type-series Diorchis serpentata von Linstow, 1905 from Calidris sp. of Western Taimyr, Russia: (D) cirrus. Scale bars: 100 mm (B), 20 mm (A, C, D).
Figure 4. Aploparaksis rissae Schiller, 1951, a in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 4. Aploparaksis rissae Schiller, 1951, a type from Rissa tridactyla, Alaska: (A) scolex, (B) hooks, (C) hermaphroditic proglottis, (D) cirrus. Scale bars: 100 mm (A, C), 50 mm, (D) 20 mm (B).
Figure 6. Aploparaksis shigini n in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 6. Aploparaksis shigini n. sp., paratype from Larus delawarensis from Alaska: (A) scolex, (B) hooks, (C) hermaphroditic proglottis, (D) cirrus, (E) egg-packet, (F) egg. Scale bars: 100 mm (A, C, E, F), 20 mm (B, D).
Figure 3. Aploparaksis larina Fuhrmann, 1921 in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 3. Aploparaksis larina Fuhrmann, 1921. Type material from Larus dominicanus, Antarctic (MHNG 62/16): (A) longitudinal sections of the strobila showing a male and a female genital ducts, (B) cirrus. Scale bars: 50 mm (A), 20 mm (B).
Figure 5. Aploparaksis shigini n in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 5. Aploparaksis shigini n. sp. Holotype from Larus ridibundus, the Rybinsk reservoir, Russia: (A) scolex, (B) hook, (C) hermaphroditic proglottis. (D) Cirrus paratype from Larus sp., Yakutiya (Spasskaya's collection, INPA, determinate as A. fusus (Krabbe, 1869): (E) cirrus, (F) hermaphroditic proglottis. Paratype from L. ridibundus from Kolyma river: (G) egg. Scale bars: 100 mm (A, C, F), 20 mm (B, D, E, G).
Figure 7. Aploparaksis shigini n in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 7. Aploparaksis shigini n. sp., paratype from L. ridibundus, Siberia: (A) live egg-packet; (B, C) live eggs. Scale bars: 200 mm (A), 30 mm (B, C).
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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.
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.