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Рис. 8. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в прироΑном парке «Шереметьевский» в 2013 г. Fig. 8. Distribution of nests of the Oriental White Stork in the Sheremetyevsky Nature Park in 2013 in The number and distribution of the Oriental White Stork Ciconia boyciana Swinhoe, 1873 in the Khabarovskiy Region
Рис. 8. РаспреΑеΛение гнезΑ ΑаΛьневосточного аиста в прироΑном парке «Шереметьевский» в 2013 г. Fig. 8. Distribution of nests of the Oriental White Stork in the Sheremetyevsky Nature Park in 2013
Figure 4 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus
Figure 4. Seasonality in breeding records of White-rumped Monjita Xolmis velatus in Brazil based on citizen science data, the literature and this study.
Figure 3 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus
Figure 3. Food delivered to nestlings of White-rumped Monjita Xolmis velatus, Rio Claro, São Paulo, Brazil. A: larva, B: Oligochaeta, C: Erythemis vesiculosa, D: Zammara tympanum, E: Lepidoptera (moth), F: Blattodea, G: Myriapoda, H: Kentropyx aff. paulensis (Luiz Carlos Ramassotti)
Figure 2 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus
Figure 2. Food delivered to nestlings of White-rumped Monjita Xolmis velatus, Rio Claro, São Paulo, Brazil. A‒C = Scarabaeidae; D = Grylloidea; E = Ensifera; F = Tettigoniidae, Conocephalinae, Copiphorini; G‒H = Lycosidae (Luiz Carlos Ramassotti)
Figure 1 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus
Figure 1. Nests of White-rumped Monjita Xolmis velatus. A: nest 1 with nestlings, Analândia, São Paulo, Brazil, 15 November 2008 (Rogério Carlos Machado); B: nest 2 with eggs, Marília, São Paulo, Brazil, 23 October 2010 (Manuel Gonzales); C‒F: nest 3, Rio Claro, São Paulo, Brazil; C: adult at entrance to PVC pipe, 20 October 2021 (Luiz Ramassotti); D: nest, 29 October 2021 (Carlos Otávio Araujo Gussoni); E: nest with nestlings, 20 October 2021 (Carlos Otávio Araujo Gussoni); F: nestling, 22 October 2021 (Carlos Otávio Araujo Gussoni)
Figure 5 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 5. Persian Shearwater Puffinus persicus persicus, off Watamu, coastal Kenya, 1 March 2022, showing the characteristic brown-toned upperparts, much-reduced white in the underwing-coverts, dusky axillaries and brown flanks streaking of this taxon (Jaap Gijsbertsen)
Figure 4 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 4. Persian Shearwater Puffinus persicus, ashore near Pangani, north-east Tanzania, 14 March 2009, showing the characteristic dusky underwing, axillaries, and faint white spot in front of the eye (© B. Simonsen)
Figure 1 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 1. Specimens of Persian Shearwater Puffinus persicus persicus (A) NMK 1442019 (Sidney Shema), (B) NMK B9189 (Sidney Shema), (C) NMK B8032 (Sidney Shema) and Tropical Shearwater Puffinus bailloni nicolae (D) AMNH 788928 (© Augie Kramer) collected in Kenya between 1963 and 2019, alongside a paratype of P. b. nicolae (E) MNHN-ZO-MO-1878-1051 (www.science.mnhn.fr/institution/mnhn/collection/zo/item/ search?lang=en_US) from the Seychelles. Birds not to scale.
Figure 3 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 3. Persian Shearwater Puffinus persicus persicus, Diani, coastal Kenya, 26 February 2019, before it died (© S. Kapila)
Figure 5 in Breeding biology, diet and vocal repertoire of White-rumped Monjita Xolmis velatus
Figure 5. Begging calls of a fledgling (A) and calls of an adult (B) White-rumped Monjita Xolmis velatus. Sonogram made using software Raven Pro 1.6.1 (Center for Conservation Bioacoustics 2019).
Figure 2 in The occurrence and status of black-and-white Puffinus shearwaters on the Kenyan and Tanzanian coasts, with the first specimen records of Persian Shearwater P. persicus persicus
Figure 2. Persian Shearwater Puffinus persicus persicus off Oman (left ML 155569281; © Marcel Gil Velasco) and United Arab Emirates (right ML 93690941; © Tommy Pedersen) alongside the December 1981 specimen from Mtwapa Creek, Kenya (centre NMK B9189; Sidney Shema), showing typical pattern of wear and fading on head producing white grizzling / streaking, and a poorly demarcated border between cheeks and throat.
Figure 1 in Release and Establishment of Encarsia diaspidicola (Hymenoptera: Aphelididae) Against White Peach Scale (Hemiptera: Diaspididae) in Papaya
Figure 1. Number of E. diaspidicola caught in individual yellow sticky traps in the Sibucao papaya field (Kapoho, Hawaii). The first releases were made in February 2013.
Figure 5 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 5: Phylogeny of Delatylus andersoni n. gen., n. sp. and closely related inferred from partial 18 S rRNA gene sequences by Bayesian analysis. Phylogeny was inferred under a GTR + I + G model (−lnL = 6333.834; AIC = 12687.668; freqA = 0.2384; freqC = 0.2036; freqG = 0.267; freqT = 0.2911; R(a) = 1.1233; R(b) = 3.698; R(c) = 2.4739; R(d) = 0.7402; R(e) = 5.1375; R(f) = 1; Pinva = 0.6096; Shape = 0.8015). Posterior probability values exceeding 50% are given on appropriate clades.
Figure 2 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 2: Micrographs of females of Delatylus andersoni n. gen., n. sp: (A) entire body; (B) head region, (C) pharynx (arrow showing the position of excretory pore and hemizonid), (D) pharynx with anterior part of the gonad, (E) posterior part of the female body, (F, G) female tail (arrow showing the position of vulva and anus), H: lateral lines. (scale bars = 10 μm).
Figure 6 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 6: Phylogeny of Delatylus andersoni n. gen., n. sp. and closely related inferred from 28 S D2/D3 rRNA gene sequences by Bayesian analysis. Phylogeny was inferred under a TrN+G model (−lnL = 2644.97; AIC = 5301.9399; freqA = 0.2103; freqC = 0.1993; freqG = 0.3249; freqT = 0.2655; R(a) = 1; R(b) = 3.0953; R(c) = 1; R(d) = 1; R(e) = 7.2585; R(f) = 1; Pinva = 0; Shape = 0.3542). Posterior probability values exceeding 50% are given on appropriate clades.
Figure 4 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 4: SEM of Delatylus andersoni n. gen., n. sp. (A, B) En face view of head and lip (aa arrows point to the amphid aperture; oa arrows point to the oral aperture; op arrows point to outer labial papillae; (C) vulva, anus, and tail; (D) lateral fields.
Figure 3 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 3: Micrographs of valve at the pharyngeal–intestinal junction of females of Delatylus andersoni n. gen., n. sp.
Fig. 8. Tabulate corals Michelinia expansa White, 1883, from locality 3 in Mississippian colonial tabulate and rugose corals from the Flett Formation, Liard Basin, northwest Canada
Fig. 8. Tabulate corals Michelinia expansa White, 1883, from locality 3 (Fig. 2), Meilleur Member, Flett Formation (Viséan, Mississipian), Rundle Group, Liard Basin, Northwest Territories, Canada. Transverse thin sections unless stated otherwise. A. IG-91-2 = UAM-Tc.Can./3; A1, fragment of colony; A2, longitudinal section (peel) of offsetting corallite; showing pores (arrows). B. IG-17 = UAM-Tc.Can./1; B1, drawing on peel image of longitudinal section of corallites in different growth stage; showing pores (grey arrows) and apparent absence of pore resulting from eccentric section (black arrow); B2, fragment of a colony. C. IG-91-1 = UAM-Tc.Can./2, different growth stages; C1, very early growth stage of offset surrounded by thick, solid wall; C2, very early growth stage of offset; showing P2 pores (black arrows) and overgrown pores? (white arrows); note differentiated thickness of partitions; C3, two offsets adjacent to one another with first dissepiments developed; C4, very early growth stage of offset with two P1 pores open to two adjacent mature corallites; C5, partitions differentiated in thickness, showing P2 pores (arrow).
Fig. 7. Tabulate coral Michelinia expansa White, 1883 in Mississippian colonial tabulate and rugose corals from the Flett Formation, Liard Basin, northwest Canada
Fig. 7. Tabulate coral Michelinia expansa White, 1883. IG-91-1 = UAM-Tc.Can./2, from locality 3 (Fig. 2), Meilleur Member, Fleet Formation (middle Viséan, Mississipian), Rundle Group, Liard Basin, Northwest Territories, Canada. A1, thin section of colony, transverse in most part and longitudinal at colony edge; A2, immature corallite, note remnants of wall microstructure, arrow points to P1 pore; A3, septal spines attached to tabula; A4, pores P1 and P 2 situated close to each other (arrows).
Fig. 4 in Morphological and molecular identification of Cryptocotyle lingua metacercariae isolated from Atlantic cod (Gadus morhua) from Danish seas and whiting (Merlangius merlangus) from the English Channel
Fig. 4 Phylogenetic trees based on cox1 mtDNA (left tree) and ITS rDNA (right tree) sequences using the ML method with 1000 bootstraps
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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.