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Fig. 4 in Assessment of coastal fish assemblages before the establishment of a new marine protected area in the central Mediterranean: its role in formulating a zoning proposal Abstract
Fig. 4: Total density (mean number of individuals/125 m2 ± S.E.) of fishes recorded along the transects at each (a) sector and (b) depth range.
Fig. 2 in Assessment of coastal fish assemblages before the establishment of a new marine protected area in the central Mediterranean: its role in formulating a zoning proposal Abstract
Fig. 2: Scatter plot of the canonical analysis of principal coordinates (CAP) based on the Bray–Curtis dissimilarities on the effects of (a) habitat type (RAR=rocky-algal reef; POM=Posidonia oceanica meadow; SOB=soft bottom) and (b) depth range.
Fig. 7. A-B. A in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records
Fig. 7. A-B. A. Diphterostomun brusinae (STOSSICH, 1888) STOSSICH, 1903 from Argyrops spinifer. Ventral view. Scale 0.5 mm. B. Cirrus sac free-hand drawing
Fig. 3. A in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records
Fig. 3. A = Monascus filiformis (RUD., 1819) from Selaroides leptolepis. Ventral view. Scale 1 mm. B = Cirrus sac free-hand composite drawing
Fig 6 in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records
Fig 6. Prosogonotrema bilabiatum PÉREZ VIGUERAS, 1940 from Epinephelus areolatus. Ventral view. Scale 1 mm
Fig. 2. A in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records
Fig. 2. A = Complexobursa vjetnamensis OSHMARIN e t MAMAEV, 1963, from Terapon theraps. Ventrolateral view. Scale 1 mm. B. Cirrus sac free-hand drawing
Fig. 1. A in Digenetic Trematodes From Marine Fishes Off The Coast Of Kuwait, Arabian Gulf: Fellodistomidae And Some Smaller Families, New Host And Geographic Records
Fig. 1. A = Lintonium vibex (LINTON, 1900) STUNKARD e t NIGRELLI, 1930, from Lagocephalus lunaris. Ventral view. Scale 1 mm. B = Cirrus sac free-hand composite drawing
Fig. 2 in Morphology and Sequence Data of Mexican Populations of the Ciliate Parasite of Marine Fishes Trichodina rectuncinata (Ciliophora: Trichodinidae)
Fig. 2. Photomicrographs of silver-impregnated adhesive discs and diagrammatic drawings of the denticles of respective morphotypes studied in the present paper; a and a'. From Enneanectes reticulatus, San Carlos, Sonora. b and b'. From Enneanectes reticulatus, San Carlos, Sonora. c and c'. From Tomicodon zebra, Zihuatanejo, Guerrero. d and d'. From Tomicodon zebra, Cuatunalco, Oaxaca.
Fig. 3 in Morphology and Sequence Data of Mexican Populations of the Ciliate Parasite of Marine Fishes Trichodina rectuncinata (Ciliophora: Trichodinidae)
Fig. 3. Bayesian inference tree of sequences of the 18S gene of trichodinid species of the genus Trichodina and Trichodinella, emphasizing on Trichodina rectuncinata. Numbers near internal nodes show the support value. Codes: ♦ Cuatunalco; * Zihuatanejo; ● San Carlos.
Fig. 1 in Morphology and Sequence Data of Mexican Populations of the Ciliate Parasite of Marine Fishes Trichodina rectuncinata (Ciliophora: Trichodinidae)
Fig. 1. Map showing the location of Mexico, and localities where populations of Trichodina rectuncinata were obtained.
Figure S4 in Spatiotemporal patterns in marine fish and cephalopods communities across scales: using an autoregressive spatiotemporal clustering model. A study of fish and cephalopods of the Eastern English Channel
Figure S4. – Spatial-temporal correlation matrix at a 782 km2 (A) and 1043 km2 (B) scale displaying correlation from strongly negative (dark blue) to strongly positive (dark red).
Figure S2 in Spatiotemporal patterns in marine fish and cephalopods communities across scales: using an autoregressive spatiotemporal clustering model. A study of fish and cephalopods of the Eastern English Channel
Figure S2. – Spatial hierarchical clustering at a 782 km2 (A) and 1043 km2 (B) scale. The rectangle outlines the communities that where find statistically significant by ASTEC given the approximately unbiased p-values expressed as proportion (red).
Figure 2 in Spatiotemporal patterns in marine fish and cephalopods communities across scales: using an autoregressive spatiotemporal clustering model. A study of fish and cephalopods of the Eastern English Channel
Figure 2. – Spatial correlation matrix at a 522 km2 scale displaying correlation from strongly negative (dark blue) to strongly positive (dark red).
Figure 11 in Spatiotemporal patterns in marine fish and cephalopods communities across scales: using an autoregressive spatiotemporal clustering model. A study of fish and cephalopods of the Eastern English Channel
Figure 11. – Scophthalmus rhombus from low (blue) to high (red) median densities of numbers/ km2 in log scale for 522 km2 for the Eastern English Channel.
Figure S5 in Spatiotemporal patterns in marine fish and cephalopods communities across scales: using an autoregressive spatiotemporal clustering model. A study of fish and cephalopods of the Eastern English Channel
Figure S5. – Spatial-temporal hierarchical clustering at a 782 km2 (A) and 1043 km2 (B) scale. The rectangle outlines the communities that where find statistically significant by ASTEC given the approximately unbiased p-values expressed as proportion (red).
Figure 2 in At the crossroads: early Miocene marine fishes of the proto-Mediterranean Sea
Figure 2. Schematic diagram of the measurements obtained on the otoliths. OL, otolith length; OH, otolith height; AL, antirostrum length; RL, rostrum length; CL, colliculum length; OCL, ostial colliculum length; CCL, caudal colliculum length; OSL, ostium length; CaL, caudal length, α, sulcus angle.
Figure 4 in At the crossroads: early Miocene marine fishes of the proto-Mediterranean Sea
Figure 4. Photographs of the identified otoliths from the Felli section. (A) Lobianchia sp., Felli 11; (B–C) Myripristis verus Steurbaut, (B) Felli 11, (C) Felli 12; (D) Echiodon heinzelini Huyghebaert and Nolf, Felli 11; (E) Apogon moyesi Steurbaut, Felli 11; (F) "Batrachoidida" vigneauxi (Steurbaut), Felli 11; (G) Blennius sp., Felli 11; (H) Arnoglossus holleri Weinfurter, Felli 11; (I) Microchirus latior (Schubert), Felli 11; (J–K) Mullus elongatus Steurbaut, (J) Felli 11, (K) Felli 12; (L) Cepola yrieuensis Steurbaut, Felli 11; (M–N) Pomadasys sp., Felli 11; (O) Pagrus sp., Felli 11. (F), (H), (J), and (K) have been mirrored to facilitate comparison.
Figure 1 in At the crossroads: early Miocene marine fishes of the proto-Mediterranean Sea
Figure 1. (A) Map of Greece where the Mesohellenic Basin is indicated. (B) Geological map of the study area: (1) Krania Formation (Eocene), (2) Eptachori Formation (lower–upper Oligocene), (3) Pentalofos Formation (upper Oligocene–lower Miocene), (4) Tsotyli Formation (middle Miocene), and (5) Quaternary. (C) Lithostratigraphic column of the Felli section with the sampled levels (modified after Zelilidis et al., 2002, and Thivaiou et al., 2019).
Figure 3 in At the crossroads: early Miocene marine fishes of the proto-Mediterranean Sea
Figure 3. Photographs of the identified otoliths from the Felli section. (A–D) Ariosoma mesohellenica sp. nov.: (A) holotype, AMPG(V) 2361, inner face and dorsal view; Felli 11; (B) paratype, AMPG(V) 2364, Felli 12; (C–D) paratypes, 2362 and 2363, Felli 11. (E–F) Ariosoma balearicum (Delaroche), Holocene, Israel. (G–H) Gnathophis elongatus sp. nov., Felli 11: (G) holotype, AMPG(V) 2365, inner face and ventral view; (H–J) paratypes, AMPG(V) 2366–2368. (K–L) Gnathophis saubriguensis (Steurbaut): (K) Felli 11, (L) Felli 12; (M– O) Spicara cf. gossei: (M) inner face and ventral view; Felli 11, (N–O) Felli 12. (C), (H), (K), (L), and (M) have been mirrored to facilitate comparison.
Fig. 3 in Molecular insights into the identification and phylogenetics of the cosmopolitan marine fish blood parasite, Haemogregarina bigemina (Adeleorina: Haemogregarinidae)
Fig. 3. Phylogenetic identification of Haemogregarina bigemina from the UK based on 18S rDNA sequences. (a) Maximum parsimony and (b) Maximum likelihood reconstructions revealing the unique position of UK H. bigemina samples outside of the adeleorine groups. For both phylogenies nodal support was calculated using 1000 bootstrap replicates with only values> 50% presented.
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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.