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Fig. 5 in Earliest Eutherian Ear Region: A Petrosal Referred to Prokennalestes from the Early Cretaceous of Mongolia
Fig. 5. Strict consensus tree of 144 equally most parsimonious trees, taken from the phylogenetic analysis by Rougier et al. (1998). Trees were obtained by using PAUP on a database of 156 craniodental characters, representing 365 morphological transformations across 48 taxa (see appendices). Six taxa were subsequently pruned from the study because of incompleteness, all being represented by only one tooth (Aegialodon, Comanchea, Trinititherium, Kermackia, Falepetrus, and Zygiocuspis). Tree length of the individual trees is 570; consistency index = 0.444; and retention index = 0.663.
Fig. 3 in Earliest Eutherian Ear Region: A Petrosal Referred to Prokennalestes from the Early Cretaceous of Mongolia
Fig. 3. Reconstruction of major arteries, veins, and nerves on the right petrosal referred to Prokennalestes trofimovi, PSSMAE 136. A, Ventral view. B, Lateral view.
Fig. 2 in Earliest Eutherian Ear Region: A Petrosal Referred to Prokennalestes from the Early Cretaceous of Mongolia
Fig. 2. Reconstruction of the osseous labyrinth of the right petrosal referred to Prokennalestes trofimovi, PSSMAE 136, in dorsal view, based on radiographs. Bone housing lateral semicircular canal and enclosing subarcuate fossa is missing.
Fig. 1 in Earliest Eutherian Ear Region: A Petrosal Referred to Prokennalestes from the Early Cretaceous of Mongolia
Fig. 1. Three views of right petrosal referred to Prokennalestes trofimovi, PSSMAE 136. A, D, Ventral view. B, E, Dorsal view. C, F, Lateral view. Given that the petrosal is both isolated and incomplete, providing the precise orientation for the bone in the complete skull is difficult. One estimate is shown here. Scale = 1 mm.
Рис. 1. А — рыжеухий бюΛьбюΛь на боярышнике, с. Δазо, Приморский край, 5.11.2019. Фото В. П. Шохрина; B — рыжеухий бюΛьбюΛь пьет сок кΛена приречного, с. Каймановка, Уссурийский гороΑской округ, Приморский край, 03.04.2022. Фото À. А. БеΛяева; C — рыжеухий бюΛьбюΛь кормится ягоΑами Αевичьего винограΑа пятиΛисточкового, г. ВΛаΑивосток, 02.01.2020. Фото А. П. ХоΑакова; D — рыжеухий бюΛьбюΛь, кΛ. ФореΛевый, окрестности с. ФиΛипповка, Хасанский район, Приморский край, 01.03.2018. Фото Ю. А. Àармана; E — рыжеухий бюΛьбюΛь кормится ягоΑами бархата амурского, г. ВΛа- Αивосток, 06.11.2019. Фото А. В. ВяΛкова; F — рыжеухий бюΛьбюΛь, с. Каймановка, Уссурийский гороΑской округ, Приморский край, 04.05.2022. Фото М. В. МасΛова Fig. 1. A — brown-eared bulbul on a hawthorn tree, Lazo village, Primorsky Region, 5.11.2019. Photo by V. P. Shokhrin; B — brown-eared bulbul drinks the juice of an Amur maple, Kaymanovka Village, Ussuriysky Urban District, Primorsky Region, 03.04.2022. Photo by D. A. Belyaev; C — brown-eared bulbul feeds on the berries of the Virginia creeper, Vladivostok, 02.01.2020. Photo by A. P. Khodakov; D — brown-eared bulbul. Forelevy spring, vicinity of Filippovka Village, Khasansky District, Primorsky Region, 01.03.2018. Photo by Yu. A. Darman; E — brown-eared bulbul feeds on the berries of an Amur cork tree, Vladivostok, 06.11.2019. Photo by A. V. Vyalkov; F — brown-eared bulbul. Kaymanovka Village, Ussuriysky Urban District, Primorsky Region, 04.05.2022. Photo by M. V. Maslov in An increase in the number of records of the brown-eared bulbul Microscelis amaurotis in the Russian Far East in recent years
Рис. 1. А — рыжеухий бюΛьбюΛь на боярышнике, с. Δазо, Приморский край, 5.11.2019. Фото В. П. Шохрина; B — рыжеухий бюΛьбюΛь пьет сок кΛена приречного, с. Каймановка, Уссурийский гороΑской округ, Приморский край, 03.04.2022. Фото À. А. БеΛяева; C — рыжеухий бюΛьбюΛь кормится ягоΑами Αевичьего винограΑа пятиΛисточкового, г. ВΛаΑивосток, 02.01.2020. Фото А. П. ХоΑакова; D — рыжеухий бюΛьбюΛь, кΛ. ФореΛевый, окрестности с. ФиΛипповка, Хасанский район, Приморский край, 01.03.2018. Фото Ю. А. Àармана; E — рыжеухий бюΛьбюΛь кормится ягоΑами бархата амурского, г. ВΛа- Αивосток, 06.11.2019. Фото А. В. ВяΛкова; F — рыжеухий бюΛьбюΛь, с. Каймановка, Уссурийский гороΑской округ, Приморский край, 04.05.2022. Фото М. В. МасΛова Fig. 1. A — brown-eared bulbul on a hawthorn tree, Lazo village, Primorsky Region, 5.11.2019. Photo by V. P. Shokhrin; B — brown-eared bulbul drinks the juice of an Amur maple, Kaymanovka Village, Ussuriysky Urban District, Primorsky Region, 03.04.2022. Photo by D. A. Belyaev; C — brown-eared bulbul feeds on the berries of the Virginia creeper, Vladivostok, 02.01.2020. Photo by A. P. Khodakov; D — brown-eared bulbul. Forelevy spring, vicinity of Filippovka Village, Khasansky District, Primorsky Region, 01.03.2018. Photo by Yu. A. Darman; E — brown-eared bulbul feeds on the berries of an Amur cork tree, Vladivostok, 06.11.2019. Photo by A. V. Vyalkov; F — brown-eared bulbul. Kaymanovka Village, Ussuriysky Urban District, Primorsky Region, 04.05.2022. Photo by M. V. Maslov
Fig. 4 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 4 Relationship between the size of bat maternity aggregation (a), percentage of forest cover (b), body condition index (c), and parasite infection of the examined bats in the Carpathians Mountains (2007).
Fig. 1 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 1 Distribution of greater mouse-eared bat (Myotis myotis) maternity aggregations (grey circles) and single founding individuals (black dots) in the Beskids (Carpathian Mountains, Poland). Data pooled from Kozakiewicz (2003), Szkudlarek et al. (2008), and our data. For the investigated maternity colonies, forested areas within a 10-km radius is shown
Fig. 3 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 3 Proportions of protonymph (PN), deutonymph (DN), and adult (AD) stages of S. myoti mites, collected from Myotis myotis (bars), and the sex ratios of deutonymph and adult mites (circles)
Fig. 2 in Is parasite load dependent on host aggregation size? The case of the greater mouse-eared bat Myotis myotis (Mammalia: Chiroptera) and its parasitic mite Spinturnix myoti (Acari: Gamasida)
Fig. 2 Micrograph of the adult female Spinturnix myoti, dorsal view. Scanning electron microscopy image, original magnification ×40
Wheat-Ears-Detection-Dataset
<p>Dataset from the Ear density estimation from high resolution RGB imagery using deep learning technique paper</p> <p> <strong>Highlights</strong><br> - 236 high resolution images (6000*4000)<br> - Wheat ears annotated with a bounding box<br> - 30729 ears identified<br> - Spatial resolution (GSD) of 0.13mm/pixel<br> - Two images for each microplots <br> - 20 contrasted genotype with 6 replicated growth in two environment</p> <p>contact : simon.madec@inra.fr </p> <p> </p> <p> </p> <p> </p> <p> </p>
Figure 1 in Selective predation on common voles by Tawny Owls and Long-eared Owls in winter and spring
Figure 1. Distribution of the body mass of Microtus arvalis individuals, trapped in October–April and preyed upon by both Strix aluco and Asio otus in winter and spring, as estimated from mandibles.
Figure 2 in Pets or predators? climate change and invasion risk of red-eared slider (Trachemys scripta elgans)
Figure 2. PCA-env for native and Indian climate for Trachemys scripta elegans. A) The green polygon represents nice unfilling, the blue polygon represents niche overlap, and the red polygon denotes nice expansion. The arrow indicates the niche centroid change. B) The correlation circle shows the relative contribution of different variables. C) and D) represent niche similarity and equivalency.
Figure 1 in Pets or predators? climate change and invasion risk of red-eared slider (Trachemys scripta elgans)
Figure 1. Predicted potential distribution of Trachemys scripta elegans under current and two future climate change scenarios.
Figure 3 in Pets or predators? climate change and invasion risk of red-eared slider (Trachemys scripta elgans)
Figure 3. Map showing species richness of native freshwater turtles at the sub-basin level in India.
Figure. PCA analysis based on GH-MspI, GH-AluI, PRL, and DGAT1 loci in Turkish native cattle breeds (Turkish Grey - TG, East Anatolian Red - EAR, Anatolian Black - AB, and South Anatolian Red - SAR). in Growth hormone (GH), prolactin (PRL), and diacylglycerol acyltransferase (DGAT1) gene polymorphisms in Turkish native cattle breeds
Figure. PCA analysis based on GH-MspI, GH-AluI, PRL, and DGAT1 loci in Turkish native cattle breeds (Turkish Grey - TG, East Anatolian Red - EAR, Anatolian Black - AB, and South Anatolian Red - SAR).
Figure 2 in The first record of alpine long-eared bat Plecotus macrobullaris in Serbia
Figure 2. External characters used for species identification: face and ears with tragus (A) and penis shape (B).
Figure 1 in The first record of alpine long-eared bat Plecotus macrobullaris in Serbia
Figure 1. Locality of the Plecotus macrobullaris record (black dot). Shaded parts of the map represent its distribution after the IUCN (Hutson et al. 2008). *This designation is without prejudice to positions on status, and is in line with UNSCR 1244/1999 and the International Court of Justice advisory opinion on Kosovo's declaration of independence.
Fig. 1 in Actions of the fire ant Solenopsis saevissima (Smith) (Hymenoptera: Formicidae) on a big-eared opossum carcass
Fig. 1. Carcass of big-eared opossum (Didelphis aurita) colonized by fire ants Solenopsis saevissima (Hymenoptera: Formicidae) and other insects on 12 Nov 2017, Juiz de Fora, Minas Gerais, Brazil. (A) Fire ants initially monopolized the carcass, constructing a dirt mound on the muzzle, thus displaying the burying behavior of the ants. (B) Circled are ants beginning construction of a soil mound near the tail. (C) Diptera depositing eggs on the carcass. Afer the carcass was moved to the periphery of the roadway, the ants lost their dominance to other necrophagous insects. (D) Skeletonized carcass; ants and other necrophagous insects remained until the end of the decomposition process.
Fig. 2 in The endocranial morphology and inner ear of the abelisaurid theropod Aucasaurus garridoi
Fig. 2. Abelisaurid theropod Aucasaurus garridoi Coria, Chiappe, and Dingus, 2002, from the Upper Cretaceous of North Patagonia (MCF-PVPH 236). Digital reconstruction of the right inner ear in lateral (A), dorsal (B), anterior (C), and posterior (D) views.
Fig. 1 in The endocranial morphology and inner ear of the abelisaurid theropod Aucasaurus garridoi
Fig. 1. Abelisaurid theropod Aucasaurus garridoi Coria, Chiappe, and Dingus, 2002 (MCF-PVPH 236), from the Upper Cretaceous of North Patagonia, in dorsal (A) and right lateral (B) views. Volume rendering of the braincase (semi-transparent) and cranial endocast (A 1, B1), and line drawings of brain and inner ear (A 2, B2).
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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.