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Fig. 6 in New record of endoparasitic Pseudempleurosoma haywardi (Monogenea: Dactylogyridae) in sillaginid fishes from Thailand, with updates on host range, zoogeography, and morphological variation
Fig. 6. Phylogenetic tree of partial 28S rRNA of monogeneans based on Maximum Likelihood methods. Two major Clades A and B are distinguished. External branches with and without round tips represent members of Dactylogyridae and Ancyrocephalidae, respectively (when classified following the NCBI database), except for the outgroup. Bootstrap support values are indicated at each node. Monogenean sequence data from this study are shown in bold. Scale bar represents the number of nucleotide substitutions per site.
Fig. 5 in New record of endoparasitic Pseudempleurosoma haywardi (Monogenea: Dactylogyridae) in sillaginid fishes from Thailand, with updates on host range, zoogeography, and morphological variation
Fig. 5. General morphology of the infected sillaginid fishes, (A) Sillago aeolus and (B) Sillago sihama. Scale bars = 1 cm.
Fig. 3 in Rediscovery of a Deep-sea Fish Parasite Lophoura cornuta (Copepoda: Sphyriidae) in the Western North Pacific off Hokkaido, Northern Japan
Fig. 3. Lophoura cornuta, adult female, NSMT-Cr 31508. A, Habitus, ventrolateral view, ethanol-preserved specimen; B, cephalothorax and part of neck including holdfast organ, ventral view; C, D, anterior part of cephalothorax, ventrolateral and dorsolateral views, respectively. The specimen was fixed in 70% ethanol on 24 March 1983 and photographed on 9 October 2023. Abbreviations: c, cephalothorax; cp, conical protuberance; ho, holdfast organ; n, neck. Scale bars: A, 10 mm; B, 3 mm; C, D, 0.5 mm.
Fig. 2 in Rediscovery of a Deep-sea Fish Parasite Lophoura cornuta (Copepoda: Sphyriidae) in the Western North Pacific off Hokkaido, Northern Japan
Fig. 2. Lophoura cornuta, adult female, NSMT-Cr 31509. A, Habitus, ventral view; B, C, cephalothorax and part of neck including holdfast organ, ventral and dorsal views, respectively; D, cephalothorax, anterior view. The trunks on the holdfast organ are individually numbered as 1, 2, 3, or 4 (B, C). Abbreviations: cp: conical protuberance; mo: mouth opening. Scale bars: A, 10 mm; B, C, 5 mm; D, 1 mm.
Fig. 1 in Rediscovery of a Deep-sea Fish Parasite Lophoura cornuta (Copepoda: Sphyriidae) in the Western North Pacific off Hokkaido, Northern Japan
Fig. 1. Collection localities of Lophoura cornuta in the western North Pacific off the south coast of Hokkaido, northern Japan, in the previous (open circle) and present (closed circles) studies. Localities 1, 2, and 3 are: off Cape Ochiishi (type locality; Wilson 1919), off Cape Shirepa (this paper), and off Shin-Hidaka (this paper), respectively.
Context-dependent multimodal behaviour in a coral reef fish: Stage 1 & 2 total duration and count data in behaviour trials
<p>Animals are expected to respond flexibly to changing circumstances, with multimodal signalling providing potential plasticity in social interactions. Whilst numerous studies have documented context-dependent behavioural trade-offs in terrestrial species, far less work has considered such decision-making in fish, especially in natural conditions. Coral reef ecosystems host 25% of all known marine species, making them hotbeds of competition and predation. We conducted experiments with wild Ambon damselfish (<em>Pomacentrus amboinensis)</em> to investigate context-dependent responses to a conspecific intruder; specifically, how nest defence is influenced by an elevated predation risk. We found that nest-defending male Ambon damselfish responded aggressively to a conspecific intruder, spending less time sheltering and more time interacting, as well as signalling both visually and acoustically. In the presence of a model predator compared to a model herbivore, males spent less time interacting with the intruder, with a tendency towards reduced investment in visual displays compensated for by an increase in acoustic signalling instead. We therefore provide ecologically valid evidence that the context experienced by an individual can affect its behavioural responses and multimodal displays towards conspecific threats.</p>
Data for: D3.6 - Assessment of organoleptic and nutritional quality of fish products from the demonstration tests
<p>Data for: D3.6 - Assessment of organoleptic and nutritional quality of fish products from the demonstration tests </p> <p>https://ifishienci.eu/wp-content/uploads/2024/01/iFishIENCi_D3.6.pdf</p> <p>Corresponding Author</p> <p>Name: Anneli Rost<br>ttz Bremerhaven, Germany<br>Address: Knurrhahnstraß 22-24 /Packhalle X 27572 Bremerhaven<br>Email: arost@ttz-bremerhaven.de</p>
Operating diagram of DR1/DR2 double riffle; it consists of two independent sections (DR1 and DR2), each containing 630 litres of water and measuring 2.5 x 0.6 m. Each section contains a filtration system separate from the fish, a cooling unit and an ultraviolet sterilizer. An 80 W UQL lamp completes the lighting of the module lit during the day. in Reproduction of Zingel asper (Linnaeus, 1758) in controlled conditions: an assessment of the experiences realized since 2005 at the Besançon Natural History Museum
Operating diagram of DR1/DR2 double riffle; it consists of two independent sections (DR1 and DR2), each containing 630 litres of water and measuring 2.5 x 0.6 m. Each section contains a filtration system separate from the fish, a cooling unit and an ultraviolet sterilizer. An 80 W UQL lamp completes the lighting of the module lit during the day.
Figure 8 in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 8. Cloacal region of Proscinetes bernardi (Thiollierè, 1852) JME 250 with the arrow pointing to the bifurcating cloacal scale present on this specimen. Scale bar = 1 cm.
Figure 6 in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 6. Majority rule consensus tree depicting the systematic position of Scalacurvichthys naishi gen. et sp. nov. holotype (SMNK-PAL. 8613) with all unordered characters based on modified database of Poyato-Ariza & Wenz (2002). Nodes are as follows: A, Pycnodontiformes; B, Brembodontidae; C, Pycnodontoidei; D, Pycnodontidae; E, Proscinitinae; F, Pycnodontinae.
Figure 4. A in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 4. A, imprint of caudal fin of Scalacurvichthys naishi gen. et sp. nov. holotype (SMNK-PAL. 8613). B, cast of caudal fin, mirrored; anterior to the right. C, camera lucida drawing based on cast of caudal fin; dashed lines indicate the restoration of incompletely preserved structures. Abbreviations: ep 1–4, epichordals 1–4; h 1–10, hypochordals 1–10; ph, parhypural. Scale bars = 1 cm.
Figure 5. A in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 5. A, cloaca of Scalacurvichthys naishi gen. et sp. nov. holotype (SMNK-PAL. 8613); dashed white lines indicate the restoration of incompletely preserved structures; tip of right branch of posterior modified cloacal scale overlain by disarticulated flank scales therefore not shown. B, camera lucida drawing; probable shape of posterior modified cloacal scale is reconstructed using dashed lines. Abbreviations: amcs, anterior modified cloacal scale; cs, cloacal scale; pcb, postcoelomic bone; pmcs, posterior modified cloacal scale; vrs, ventral ridge scale. Scale bars = 1 cm.
Figure 3 in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 3. Skull of Scalacurvichthys naishi gen. et sp. nov., holotype (SMNK-PAL. 8613) under UV light in order to show the preserved remains of the posterior exposed endocranium to which the arrow points. Scale bar = 1cm.
Figure 2. A in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 2. A, skull of Scalacurvichthys naishi gen. et sp. nov., holotype (SMNK-PAL. 8613) with forward-facing first dorsal ridge scale. B, camera lucida drawing showing restored position of scale tip in life. C, camera lucida drawing of first dorsal ridge scale as it is seen in the holotype showing original position of the tip of the spine. D, restoration of first two dorsal ridge scales revealing probable morphology; dashed lines indicate the restoration of incompletely preserved structures. Abbreviations: 1st drs, 1st dorsal ridge scale; ang, angular bone; art, articular bone; cp, coronoid process; den, dentalosplenial; dhyo, dermohyomandibular; dps, dermopterosphenotic; dso, dermosupraoccipital; endo, posteriorly exposed endocranium; mes, mesethmoid; met, metapterygoid; or, orbit; pa, parietal; pap, post-parietal process; pm, premaxilla; pp, post-parietal bone; pra, prearticular bone; pre, preoperculum; ps, parasphenoid process; sc, sclerotic ring; vo, vomer. Scale bars: A–C = 1 cm; D = 50 mm.
Figure 1. A in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 1. A, Scalacurvichthys naishi gen. et sp. nov., holotype (SMNK-PAL. 8613). B, camera lucida drawing of Scalacurvichthys naishi gen. et sp. nov.; dashed lines indicate the restoration of incompletely preserved structures; bones shaded in grey are reconstructions while the rest of the drawing is the original specimen. Scale bars = 1 cm.
Figure 7 in A new pycnodont fish, Scalacurvichthys naishi gen. et sp. nov., from the Late Cretaceous of Israel
Figure 7. Cloacal region of Stemmatodus rhombus (Heckel, 1854) MNHN JRE 41 with the arrows pointing to the bifurcated scales anterior and posterior to the cloaca. Dashed line indicates boundary between ventral ridge scale and bifurcated posterior modified cloacal scale. Scale bar = 50 mm.
Figure 7 in Before the freeze: otoliths from the Eocene of Seymour Island, Antarctica, reveal dominance of gadiform fishes (Teleostei)
Figure 7. Fossil otolith record in Antarctica, Australia, New Zealand and the North Sea Basin and distribution and estimated abundance of gadiform otoliths (number of species, recognized or inferred, not shown). Ranicipitidae shown in family ranking following Nelson (1994); other families following Nelson (2006). Data compiled and altered from Nolf (2013), Schwarzhans (1980, 1985, 1994, 2003) and Stinton (1965, 1966).
Figure 6. Eocene otoliths from Seymour Island. A in Before the freeze: otoliths from the Eocene of Seymour Island, Antarctica, reveal dominance of gadiform fishes (Teleostei)
Figure 6. Eocene otoliths from Seymour Island. A, Argentina antarctica sp. nov., holotype, NRM-PZ P.15964, mirror imaged, inner face. B, C, Diaphus? marambionis sp. nov., holotype, NRM-PZ P.15966; B, inner face; C, ventral view. D—F, Macruronus eastmani sp. nov., holotype, NRM-PZ P.15970, mirror imaged; D, inner face; E, ventral view; F, outer face. G—I, Palimphemus seymourensis sp. nov., holotype, NRM-PZ P.15973, mirror imaged; G, inner face; H, ventral view; I, outer face. J—L, Coelorinchus nordenskjoeldi sp. nov., holotype, NRM-PZ P.15978; J, inner face; K, ventral view; L, outer face. M, N, Coelorinchus balushkini sp. nov., holotype, NRM-PZ P.15976; M, inner face; N, ventral view. O, P, Hoplobrotula? antipoda sp. nov., holotype, NRM-PZ P.15984, mirror imaged; O, inner face; P, ventral view. Q, Notoberyx cionei gen. nov., sp. nov.; holotype, NRM-PZ P.15987, inner face. R, Cepola anderssoni sp. nov., holotype, NRM-PZ P.15996, mirror imaged, inner face.
Figure 5 in Before the freeze: otoliths from the Eocene of Seymour Island, Antarctica, reveal dominance of gadiform fishes (Teleostei)
Figure 5. Drawings of Eocene otoliths from Seymour Island. A—C, Hoplobrotula? antipoda sp. nov.; A, B, holotype, NRM-PZ P.15984, mirror imaged; A, inner face; B, ventral view; C, paratype, NRM-PZ P.15985, inner face. D—G, Notoberyx cionei gen. nov., sp. nov.; D—F, holotype, NRM-PZ P.15987; D, anterior view; E, inner face; F, ventral view; G, paratype, NRM-PZ P.15988, inner face. H, Centroberyx sp., NRM-PZ P.15986, mirror imaged, inner face. I, J, Acanthopterygii indet., NRM-PZ P.15990, mirror imaged; I, inner face, J, ventral view. K, L, Percoidei indet., NRM-PZ P.15992, mirror imaged; K, inner face; L, ventral view. M, N, Haemulidae? indet., NRM-PZ P.15993, mirror imaged; M, inner face; N, ventral view. O, P, Sparidae? indet., NRM-PZ P.15994, mirror imaged; O, inner face; P, ventral view. Q, R, Cepola anderssoni sp. nov., holotype, NRM-PZ P.15996, mirror imaged; Q, inner face; R, ventral view.
Figure 4 in Before the freeze: otoliths from the Eocene of Seymour Island, Antarctica, reveal dominance of gadiform fishes (Teleostei)
Figure 4. Drawings of Eocene otoliths from Seymour Island. A, B, Tripterophycis immutatus Schwarzhans, 1980, NRM-PZ P.15969, mirror imaged; A, inner face; B, dorsal view. C—F, Macruronus eastmani sp. nov.; C—E, holotype, NRM-PZ P.15970, mirror imaged; C, inner face; D, outer face; E, ventral view; F, paratype, NRM-PZ P.15971, inner face. G—M, Palimphemus seymourensis sp. nov.; G—I, holotype, NRM-PZ P.15973, mirror imaged; G, inner face; H, ventral view; I, outer face; J, paratype, NRM-PZ P.15975, mirror imaged, inner face; K—M, paratypes, NRM-PZ P.15974; K, inner face, mirror imaged; L, ventral view; M, inner face. N—R, Coelorinchus nordenskjoeldi sp. nov.; N—P, holotype, NRM-PZ P.15978; N, inner face; O, ventral view; P, outer face; Q, R, paratype, NRM-PZ P.15979, mirror imaged; Q, inner face; R, ventral view. S—U, Coelorinchus balushkini sp. nov., holotype, NRM-PZ P.15976; S, inner face; T, ventral view; U, outer face. V, W, Coelorinchus sp., NRM-PZ P.15911; V, inner face (strongly eroded); W, ventral view.
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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.