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Figure 1 in Impact of alien fishes on the distribution pattern of indigenous freshwater fishes of Punjab, Pakistan
Figure 1. Map of sampling sites along with four sampling sites i.e. Head Qadirabad (HQ), Head Baloki (HB), Islam Headworks (IH) and Rasul Barrage (RB).
Рис. 4. РаспреΑеΛение рыб в верхнем и нижнем бьефе в периоΑ осенней миграции 2018 г. (а) и верхнем бьефе в весеннюю миграцию 2019 г. (б). Точками показаны места фиксации рыб эхоΛотом Fig. 4. Distribution of fish upstream and downstream of the reservoir during the autumn migration of 2018 (а) and upstream of the reservoir during the spring migration of 2019 (b). Points indicate the locations where fish were registered by echosounder in Dynamics and current status of the Amazar River ichthyofauna after the construction of the PPM «Polyarnaya» hydroelectric complex
Рис. 4. РаспреΑеΛение рыб в верхнем и нижнем бьефе в периоΑ осенней миграции 2018 г. (а) и верхнем бьефе в весеннюю миграцию 2019 г. (б). Точками показаны места фиксации рыб эхоΛотом Fig. 4. Distribution of fish upstream and downstream of the reservoir during the autumn migration of 2018 (а) and upstream of the reservoir during the spring migration of 2019 (b). Points indicate the locations where fish were registered by echosounder
Рис. 5. РаспреΑеΛение рыб в верхнем бьефе воΑохраниΛища по размерным группам в периоΑ осенней миграции. Размеры рыб: а — меΛкие (Αо 10 см); б — среΑние (10–20 см); в — крупные (боΛее 20 см) Fig. 5. Distribution of fish upstream of the reservoir by size during the autumn migration. Fish sizes: а — small (under 10 cm); b — medium (10–20 cm); c — large (exceeding 20 cm) in Dynamics and current status of the Amazar River ichthyofauna after the construction of the PPM «Polyarnaya» hydroelectric complex
Рис. 5. РаспреΑеΛение рыб в верхнем бьефе воΑохраниΛища по размерным группам в периоΑ осенней миграции. Размеры рыб: а — меΛкие (Αо 10 см); б — среΑние (10–20 см); в — крупные (боΛее 20 см) Fig. 5. Distribution of fish upstream of the reservoir by size during the autumn migration. Fish sizes: а — small (under 10 cm); b — medium (10–20 cm); c — large (exceeding 20 cm)
Fig. 1. Circular Bayesian tree inferred from mtDNA cox-2 in Temporal stability of parasite distribution and genetic variability values of Contracaecum osculatum sp. D and C. osculatum sp. E (Nematoda: Anisakidae) from fish of the Ross Sea (Antarctica)
Fig. 1. Circular Bayesian tree inferred from mtDNA cox-2 sequences obtained from specimens of C. osculatum sp. D and C. osculatum sp. E analysed in the present study, based on Bayesian Inference (BI) method using MrBayes v3.2.2 (Ronquist et al., 2012). Evolutionary distance was estimated using the TrN + G (G = 0.60) substitution model as implemented in jModeltest (Posada, 2008), with the AIC approach (Posada and Buckley, 2004). Posterior probability values are the result of 1.000000 of runs and are reported at the nodes. The coloured icons correspond to the two species considered in this study (red = C. osculatum sp. D and blue = C. osculatum sp. E).
Fig. 2 in Temporal stability of parasite distribution and genetic variability values of Contracaecum osculatum sp. D and C. osculatum sp. E (Nematoda: Anisakidae) from fish of the Ross Sea (Antarctica)
Fig. 2. Schematic distribution of the fish species examined in the present study for larval of C. osculatum sp. D and C. osculatum sp. E, along the continental shelf of the Ross Sea coastal ecosystem. Arrows indicating preferred preys and the diet preference for each fish species are reported according to the literature (La Mesa et al., 2004). The represented pelagic organisms comprise species of euphausiids and fish juveniles, benthic and epibenthic organisms are polychaetes, amphipods, decapods and gastropods. A pie chart with the relative proportions of C. osculatum sp. D and C. osculatum sp. E is given for each fish species. Squares and circles represent the hypothetical distribution of C. osculatum sp. D and C. osculatum sp. E larvae in their intermediate hosts.
Fig. 3 in Temporal stability of parasite distribution and genetic variability values of Contracaecum osculatum sp. D and C. osculatum sp. E (Nematoda: Anisakidae) from fish of the Ross Sea (Antarctica)
Fig. 3. Schematic representation of the hypothetic life-cycle of C. osculatum sp. D (a) and C. osculatum sp. E (b) in the Ross Sea.
Fig. 3 in Alien freshwater fish parasites from South Africa: Diversity, distribution, status and the way forward
Fig. 3. Maps indicating the South African distribution records for (A) Atractolytocestus huronensis Anthony, 1958; (B) Acolpenteron ureteroecetes Fischthal and Allison, 1940; (C) Dactylogyrus extensus Mueller and Van Cleave, 1932, Dactylogyrus minutus Kulwiec, 1927 and Dactylogyrus lamellatus Achmerow, 1952; (D) Gyrodactylus kherulensis Ergens, 1974.
Fig. 1 in Alien freshwater fish parasites from South Africa: Diversity, distribution, status and the way forward
Fig. 1. Maps indicating the South African distribution records for (A) Ichthyophthirius multifiliis Fouquet, 1876; (B) Apiosoma piscicola (Blanchard, 1885); (C) Chilodonella hexasticha (Kiernik, 1909) and Chilodonella piscicola (Zacharias, 1894); (D) Schyzocotyle (Bothriocephalus) acheilognathi (Yamaguti, 1934).
Fig. 2 in Alien freshwater fish parasites from South Africa: Diversity, distribution, status and the way forward
Fig. 2. Maps indicating the South African distribution records for (A) Lernaea cyprinacea Linnaeus, 1758; (B) Argulus japonicus Thiele, 1900; (C) Ichthyobodo necator Henneguy, 1883 (needs molecular confirmation); (D) Trichodina acuta Lom, 1961, Trichodina mutabilis Kazubski and Migala, 1968, Trichodina reticulata Hirschmann and Partsch, 1955, and Trichodina uniforma Van As and Basson, 1989.
Figure 4 in Diadromous fishes from Saint-Pierre and Miquelon archipelago: diagnoses, taxonomy, nomenclature and distribution
Figure 4. – Pungitius pungitius (Linnaeus, 1758): syntypes LSL 34 and 35; scale bar = 1cm; with the permission of the Linnean Society of London (A); MNHN-IC-2022-0020, 32.7 mm SL, Saint-Pierre and Miquelon, Saint-Pierre Island, Milieu Pond (B).
Figure 2. – Mean abundance per 750 m2 in Changes in distribution patterns of two vulnerable fish species (Epinephelus marginatus and Sciaena umbra) in the Scandola marine reserve (Corsica, NW Mediterranean): a possible effect of increased boat tourism
Figure 2. – Mean abundance per 750 m2 (± SE) of the dusky grouper Epinephelus marginatus (A) and the brown meagre Sciaena umbra (B) according to protection level at Scandola in 2012 and 2018. IR: integral reserve, BZ: buffer zone, UP: unprotected zone. Interannual difference are indicated for each protection level, *: significant at p <0.05, ns: not significant.
Figure 3 in Diadromous fishes from Saint-Pierre and Miquelon archipelago: diagnoses, taxonomy, nomenclature and distribution
Figure 3. – Gasterosteus aculeatus Linnaeus, 1758: syntypes LSL 29-31; scale bar = 1cm; with the permission of the Linnean Society of London (A); MNHN-IC-2022-0022, 33.7 mm SL, Saint-Pierre and Miquelon (B).
Figure 2 in Diadromous fishes from Saint-Pierre and Miquelon archipelago: diagnoses, taxonomy, nomenclature and distribution
Figure 2. – Apeltes quadracus (Mitchill, 1815): drawning of an individual from New York, USA given by Mitchill (1815: 430, Pl. 1) with its species description (A); MNHN-IC-2022-0021, 26.9 mm SL, Saint-Pierre and Miquelon, Saint-Pierre Island, Airport Pond (B).
Figure 1 in Changes in distribution patterns of two vulnerable fish species (Epinephelus marginatus and Sciaena umbra) in the Scandola marine reserve (Corsica, NW Mediterranean): a possible effect of increased boat tourism
Figure 1. – Location of sites surveyed for dusky grouper and brown meagre populations inside and outside the Scandola MNR (Corsica, NW Mediterranean), according to protection status in summer 2012 and 2018. Dark blue arrows = integral reserve (IR), light blue arrows = buffer zone (BZ), red arrows = unprotected zones (UP). Blue stars = surveyed only in 2012, red star = site surveyed only in 2018.
Figure 5 in Changes in distribution patterns of two vulnerable fish species (Epinephelus marginatus and Sciaena umbra) in the Scandola marine reserve (Corsica, NW Mediterranean): a possible effect of increased boat tourism
Figure 5. – Size structure of Epinephelus marginatus and Sciaena umbra at Scandola in 2012 and 2018. Size classes = 10 cm for the dusky grouper and 5 cm for the brown meagre.
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group. in Distribution of extracellular enzyme-producing bacteria in the digestive tracts of 4 brackish water fish species
Figure. The phylogenetic tree showing the relationship among Brevibacillus parabrevis strains SA2.2 and TJ2.3, Bacillus licheniformis MG4.2, and their phylogenetically closest type strains. The GenBank accession numbers of the type strains and studied strains are shown following species names. Distance matrix was calculated by Kimura's 2-parameter model. The scale bar indicates 0.02 substitutions per nucleotide position. Alicyclobacillus pohliae AJ564766 served as an out-group.
Fig. 3 in New insight into the distribution and palaeobiology of the pycnodont fish Gyrodus
Fig. 3. Late Jurassic pycnodonts to exemplify the body form and arrangement of unpaired fins. A. Gyrodus hexagonus (de Blainville, 1818) (JME SOS 3163) from the Tithonian of Eichstätt, southern Germany. B. Apomesodon gibbosus (Wagner, 1851) (JME SOS 3572a) from the Tithonian of Eichstätt, southern Germany. Scale bars 5 cm.
Fig. 2 in New insight into the distribution and palaeobiology of the pycnodont fish Gyrodus
Fig. 2. Dental remains of Gyrodus spp. A. Right prearticular dentition of Gyrodus sp. (NLH 102.971) from the lower Barremian of clay pit "Gott"; occlusal (A1), mesial (A2), and lateral (A3) views. B. Fragmentary prearticular dentition of Gyrodus sp. (NLH 102.972) from the Hauterivian of clay pit "Engelbostel"; occlusal view. C. Articulated prearticulars of Gyrodus hexagonus (de Blainville, 1818) (MB.f. 1345) from the Kimmeridgian of Solnhofen, Bavaria; occlusal view. D. Posterior principle prearticular teeth of Gyrodus hexagonus (de Blainville, 1818) (BSP−AS VII 1073) from the Kimmeridgian of Solnhofen, Bavaria; occlusal view. E. Latero−posterior prearticular tooth of Gyrodus hexagonus (de Blainville, 1818) (MB.f. 1367) from the Kimmeridgian of Solnhofen, Bavaria; occlusal view. F. Left prearticular of Gyrodus circularis Agassiz, 1844 (JM SOS 3130) from the Kimmeridgian of Wintershof, Bavaria; occlusal view. G. Unidentified pycnodont vomer (aff. Gyrodus? sp.) (MB.f. 7133) from the Hauterivian, Lower Cretaceous, of Langenberg near Oker, northern Germany; occlusal view. H. Left prearticular of an unidentified pycnodont (aff. Gyrodus? sp.) (MB.f. 7233) from an Lower Cretaceous erratic of the Baltic Sea; occlusal view. Scale bars 5 mm.
Fig. 1 in New insight into the distribution and palaeobiology of the pycnodont fish Gyrodus
Fig. 1. General sketch map of Germany (A) with position of the clay pits "Gott" and "Engelbostel" (B) that yielded the dental remains described herein. Abbreviations: E, clay pit "Engelbostel"; G, clay pit "Gott"; H, Hanover.
Fig. 4 in Mapping a brain parasite: occurrence and spatial distribution in fish encephalon
Fig. 4. Transmission electron micrographs showing the tegument and capsule walls of metacercariae of Cardiocephaloides longicollis. A and F illustrate the capsule wall of monocyst and multicyst metacercariae; B and I represent diagrams of monocyst and multicyst metacercariae showing the location of the following TEM micrographs. C – E Longitudinal section through the capsule wall and tegument of a monocyst. G, H, J-M Longitudinal section through the inner capsule wall and tegument of a multicyst metacercaria. D, E, J-M Detail of necrotic material accumulated on the capsule wall surrounding the metacercaria. K, Detail of inner capsule walls merging together within a multicyst. CW, capsule wall; F, fibrocyte; Gx, glycocalyx; GxF, glycocalyx filaments; ICW, inner capsule wall; M, metacercaria; M1- M3 number of metacercaria in a multicyst; MA, macrophage; Mt, metacercarial tegument; N, nucleus; NC, necrotic cells. Head arrows indicate glycocalyx filaments, asterisks (*) outside of the cyst, (**) inside of the cyst, (***) inside of the cyst when encysted with more than one capsule wall. Scale bars: D, E = 1 μm; C, G, H, J, L, M = 5 μm; K = 10 μm.
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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.