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Fig. 5 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 5. Dorsal (top), lateral (middle), and ventral (bottom) views of head of Rhinogobius aonumai aonumai stained with cyanine blue showing cephalic sensory pores and papillae. OMNH-P 40256, holotype, male, 65.9 mm SL Red circles with red letters indicate sensory canal pores (letters with prime marks indicate terminal openings of sensory canals); rows of yellow spots indicated by yellow letters represent sensory papillae rows; black arrows show ventralmost positions of gill opening. Abbreviations: AN, anterior narial pore; PN, posterior narial pore. Photographed and annotated by T. Suzuki.
Fig. 3 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 3. Ventral view of pelvic fin (A) and dorsal view of head (B), in Rhinogobius aonumai aonumai stained with Alizarin Red S. OMNH-P 43694, paratype, male, 70.5 mm SL. White lines indicate position where proximal most segment of each branch alignes transversely with the fifth segmented ray. Black wedge indicates slits between branches. Black circles with black letters H′, K′, and L′ indicate sensory-canal pores. P1, P2, and P3 indicate anteriormost point of anterior extension of scaly area along predorsal midline, anteriormost point of anterior extensions of scaly area on temporal region, and greatest concaved point of scaly area between P1 and P2, respectively. Photographed and annotated by T. Suzuki.
Fig. 7 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 7. Freshly-collected paratypes of Rhinogobius aonumai aonumai from Iriomote-jima Island, the Ryukyu Islands, Japan. Nakaragawa River: A (OMNH-P 43153, male, 47.3mm SL) and B (OMNH-P 43156, female, 37.0 mm SL); Nishida-gawa River: C (OMNH-P 40533, male, 58.3 mm SL) and D (OMNH-P 40537, female, 50.3 mm SL); Urauchi-gawa River: E (OMNH-P 40040, male, 43.6 mm SL) and F (SPMN-PI 46249, female, 46.0 mm SL); Yuchin-gawa River: G (OMNH-P 40323, male, 63.0 mm SL) and H (OMNH-P 40327, female, 49.2 mm SL). Photographed by T. Suzuki.
Fig. 16 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 16. Rhinogobius flumineus at Ina-gawa River, Ina-gawa, Hyogo Prefecture, Japan. Freshly-collected: A (OMNH-P 43228, 52.3 mm SL, male) and B (OMNH-P 43229, 50.6 mm SL, female), photographed by T. Suzuki.; underwater photographs: C (male, about 40 mm SL) and D (female, about 40 mm SL), photographed by M. Suzuki.
Fig. 13 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 13. Dorsal (top), lateral (middle), and ventral (bottom) views of head of Rhinogobius aonumai ishigakiensis stained with cyanine blue showing cephalic sensory pores and papillae. KPM-NI 65588, paratype, male, 55.9 mm SL. Red circles with red letters indicate sensory canal pores (letters with prime marks indicate terminal openings of sensory canals); rows of yellow spots indicated by yellow letters represent sensory papillae rows; black arrows show ventralmost positions of gill opening. Abbreviations: AN, anterior narial pore; PN, posterior narial pore. Photographed and annotated by T. Suzuki.
Fig. 4 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 4. Lateral view of body (A, C) and ventral view of belly (B, D) in Rhinogobius aonumai aonumai stained with Alizarin Red S. A and B: NSMT-P 138485, paratype, male, 56.0 mm SL, Hinai-gawa River; C and D: OMNH-P 40852, paratype, male, 47.5 mm SL, Aira-gawa River. Pink spots indicate the lateral anterior margin of ctenoid scale area. Photographed and annotated by T. Suzuki.
Fig. 1 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 1. Holotype of Rhinogobius aonumai aonumai (OMNH-P 40256, male, 65.9 mm SL) collected from Hinai-gawa River, Iriomotejima Island, the Ryukyu Islands, Japan. A and B: freshly-collected; C: alcohol-preserved. Photographed by T. Suzuki.
Fig. 2 in A New Species with Two New Subspecies of Rhinogobius (Teleostei: Gobiidae) from Yaeyama Group, the Ryukyu Islands, Japan
Fig. 2. Female paratype of Rhinogobius aonumai aonumai (KPM-NI 59988, 56.5 mm SL) collected from Hinai-gawa River, Iriomotejima Island, the Ryukyu Islands, Japan. A and B: freshly-collected; C: alcohol-preserved. Photographed by T. Suzuki.
Fig. 5 in Taxonomic groups with lower movement capacity may present higher beta diversity
Fig. 5. Similarity in species composition of birds among the 16 localities sampled in Minas Gerais, Brazil, based on the Jaccard coefficient of similarity and subsequent cluster analysis (UPGMA). Obs.: dashed line (significance level: 0.5 or 50%) (AIU, Aiuruoca; BOC, Bocaina de Minas; CAM, Camanducaia; CAX, Caxambu; DEL, Delfim Moreira; EXT, Extrema; GUA, GuaxupÉ; MAR, Maria da FÉ; MON, Monte Belo; MVE, Monte Verde; PAS, Passa Quatro; POÇ, Poços de Caldas; POU, Pouso Alegre; SGS, SÃo Gonçalo do SapucaÍ; SRJ, Santa Rita de Jacutinga; VIR, VirgÍnia).
Fig. 6 in Taxonomic groups with lower movement capacity may present higher beta diversity
Fig. 6. Similarity in species composition of primates among the 16 localities sampled in Minas Gerais, Brazil, based on the Jaccard coefficient of similarity and subsequent cluster analysis (UPGMA). Obs.: dashed line (significance level: 0.5 or 50%) (AIU, Aiuruoca; BOC, Bocaina de Minas; CAM, Camanducaia; CAX, Caxambu; DEL, Delfim Moreira; EXT, Extrema; GUA, GuaxupÉ; MAR, Maria da FÉ; MON, Monte Belo; MVE, Monte Verde; PAS, Passa Quatro; POÇ, Poços de Caldas; POU, Pouso Alegre; SGS, SÃo Gonçalo do SapucaÍ; SRJ, Santa Rita de Jacutinga; VIR, VirgÍnia).
Fig. 5 in A new lizard of the Liolaemus montanus group that inhabits the hyperarid desert of southern Peru
Fig. 5. Terra typica of Liolaemus basadrei. Valle de Locumba, 897 m, Jorge Basadre Province, Region Tacna, Perú.
Fig. 2 in A new lizard of the Liolaemus montanus group that inhabits the hyperarid desert of southern Peru
Fig. 2. Dorsal (A) and ventral (B) views of holotype specimen collected in Valle de Locumba, Jorge Basadre Province, Region Tacna, Peru. Dorsal (C) and ventral (D) views of allotype specimen collected in Valle de Locumba, Jorge Basadre Province, Region Tacna, Peru.
Fig. 4 in A new lizard of the Liolaemus montanus group that inhabits the hyperarid desert of southern Peru
Fig. 4. Current (star) and potential (in gray) distributions of Liolaemus basadrei in the Jorge Basadre Province, Tacna, Peru, obtained from the MAxEnt algorithms.
Data for: Manta rays in the Maldives foraging either in groups or solo
<p>Flexibility in animal foraging strategies can increase overall feeding efficiency. For example, group foraging can increase the efficiency of resource exploitation; conversely, solo foraging can reduce intraspecific competition, particularly at low resource densities. The cost-benefit trade-off of such flexibility is likely to differ within and among individuals. Reef manta rays (<em>Mobula alfredi</em>) are large filter-feeding elasmobranchs that often aggregate to feed on ephemeral upwellings of zooplankton. Over three years in the Maldives, we free-dived to film 3106 foraging events involving 343 individually identifiable <em>M. alfredi</em>. Individuals fed either solo or in groups with a clear leader plus between one and eight followers. <em>M. alfredi</em> were significantly more likely to forage in groups than solo at high zooplankton levels, and at certain locations. Both biotic and abiotic factors contributed to variation in group foraging. Within aggregations, individuals foraged in larger groups when more food was available, and when the overall aggregation was relatively small suggesting that foraging in large groups was more beneficial when food was abundant, and/or the costs of intraspecific competition were outweighed by the efficiency resulting from group foraging strategies. Females, the larger sex, were more likely to lead foraging groups than males. The high within-individual variance (over 55%), suggested individuals were unpredictable across all foraging behaviours, thus individual <em>M. alfredi</em> cannot be classified into foraging types or specialists. Instead, each individual was capable of considerable behavioural flexibility, as predicted for a species reliant on spatially and temporally ephemeral resources.</p>
Fig. 3 in A new species of Tantilla of the taeniata group (Squamata: Colubridae) from Refugio de Vida Silvestre Barras de Cuero y Salado in Caribbean coastal Honduras
Fig. 3. Distribution of the species of the Tantilla taeniata group in Honduras. The star indicates the type locality of Tantilla lydia sp. nov. The most northwestern location of Tantilla gottei was recently published by Orellana Murillo et al. (2020).
Fig. 2 in A new species of Tantilla of the taeniata group (Squamata: Colubridae) from Refugio de Vida Silvestre Barras de Cuero y Salado in Caribbean coastal Honduras
Fig. 2. Dorsal (A), lateral (B), and ventral (C) views of the head and nape of the holotype of Tantilla lydia sp. nov. (UVS-V 1189). Photos by Cristopher Antúnez-Fonseca.
Fig. 1 in A new species of Tantilla of the taeniata group (Squamata: Colubridae) from Refugio de Vida Silvestre Barras de Cuero y Salado in Caribbean coastal Honduras
Fig. 1. Dorsolateral view of the holotype of Tantilla lydia sp. nov. (UVS-V 1189) in life. Photo by Cristopher Antúnez-Fonseca.
Fig. 4 in A new species of Tantilla of the taeniata group (Squamata: Colubridae) from Refugio de Vida Silvestre Barras de Cuero y Salado in Caribbean coastal Honduras
Fig. 4. Type locality and surrounding habitat for Tantilla lydia sp. nov. showing the train tracks where the holotype was collected, Comunidad de Salado Barra, La Unión, Departamento de Atlántida, Honduras. Photo by Cristopher Antúnez-Fonseca.
Raw GNSS data divided into observation data in CRX, RINEX and mat format and navigation data in SP3 format and both group of the data in mat format
Open the record for dataset details and reuse information.
FIGURE 26 in A Revision of the rhopalocerus Species Group of Bembecinus Costa (Hymenoptera: Crabronidae: Bembicinae)
FIGURE 26. Collecting records of Bembecinus spp.: a – quadristrigatus, b – rhopaloceroides, c – rhopalocerus, d – somalicus, e – zebratus, f – all species combined.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.