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74 results for “Cyclophyllidea”
Figs 6-9 in Two new species of Cestoda (Cyclophyllidea: Dilepididae) from Ploceidae and Passeridae (Aves: Passeriformes) in Côte d'Ivoire
Figs 6-9. Monopylidium comoensis sp. nov. (6) Scolex. (7) Rostellar hook. (8) Mature proglottis, dorsal view (9) Terminal genitalia. Scale bars: 6, 9: 50 µm; 7: 10 µm; 8: 100 µm.
Figs 1-5 in Two new species of Cestoda (Cyclophyllidea: Dilepididae) from Ploceidae and Passeridae (Aves: Passeriformes) in Côte d'Ivoire
Figs 1-5. Spiniglans thomassankara sp. nov. (1) Scolex. (2) Rotellar hooks. (3) Mature proglottis, ventral view; (4) Terminal genitalia. (5) Egg. Scale bars: 1, 3: 100 µm; 2: 50 µm; 4, 5: 20 µm.
Fig. 2 in A New Genus And Species Of Cestodes (Cyclophyllidea, Gryporhynchidae) From Ciconiiform Birds
Fig. 2. Proparadilepis plegadissaakovae gen. et sp. n. Holotype: 1— scolex; 2 — rostellar hooks; 3 — egg; 4 — hermaphrodyte proglottid; 5 — gravid proglottid. Scale bars 1, 4, 5 — 100 µm; 2, 3 — 50 µm.
Fig. 1 in A New Genus And Species Of Cestodes (Cyclophyllidea, Gryporhynchidae) From Ciconiiform Birds
Fig. 1. Proparadilepis plegadissaakovae gen. et sp. n. Holotype, general view of cestoda. Scale bar 1 cm.
Fig. 4 in A New Genus And Species Of Cestodes (Cyclophyllidea, Gryporhynchidae) From Ciconiiform Birds
Fig. 4. Armament of scolex: 1 — Paradilepis scolecina (Rudolphi, 1819) Hsü, 1935; 2 — Moshonalepis macrosphincter (Fuhrmann, 1909) comb. n.; 3 — Proparadilepis plegadissaakovae gen. et sp. n. Scale bars 100 µm.
Fig. 3 in A New Genus And Species Of Cestodes (Cyclophyllidea, Gryporhynchidae) From Ciconiiform Birds
Fig. 3. Proparadilepis plegadissaakovae gen. et sp. n. Holotype (copulatory apparatus): 1— cirrus partly invaginated; 2 — cirrus and vagina. Scale bars: 1 —50 µm; 2 —100 µm.
Fig. 1 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): origin, differentiation and functional ultrastructure of the oncospheral tegument and hook region membrane
Fig. 1 Schematic diagram illustrating the origin (a) and beginning of differentiation (b) of the oncospheral tegument and hook region membrane in the preoncospheral stage of embryonic development of Echinococcus multilocularis. All structures involved in formation of the oncospheral tegument and hook region membrane are marked in orange colour. Two red arrows show direction of progressive sinking or migration of the binucleate subtegumental perikaryon which sunk deep into the central region of differentiating oncosphere. HFC hook-forming cell or oncoblast, HP hook primordium, HRC hook region cavity, IE inner envelope, m mitochondria, N1, N2 two nuclei of the binucleate complex primordium, N nucleus of hook-forming cell, PBC binucleate complex primordium, V vesicles in the outer cytoplasm, undergoing progressive fusion
Fig. 6 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): origin, differentiation and functional ultrastructure of the oncospheral tegument and hook region membrane
Fig. 6 TEM micrographs of mature eggs of Echinococcus multilocularis. a Part of the oncosphere showing the high concentration of beta-glycogen particles (β-gl) in the musculature of oncospheral hooks (HM) as indicated by the cytochemical test of Thiéry. b Low-power electron micrograph illustrating the general topography of mature intrauterine egg. Note: (1) a bilateral symmetry of the oncosphere (white interrupted line) and (2) position of hook region membrane and oncospheral tegument at one pole of the hexacanth. The hook region is marked by a frame composed of interrupted black lines. EmB embryophoric blocks, GC germinative cells, GL granular layer, HRM hook region membrane, IE inner envelope, LH lateral hooks, MH median hooks, OE outer envelope, OM oncospheral membrane, PG penetration glands, SC somatic cells
Fig. 5 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): origin, differentiation and functional ultrastructure of the oncospheral tegument and hook region membrane
Fig. 5 High-power TEM micrographs showing ultrastructural details of the oncospheral tegument and hook region membrane. a Note two oblique sections of blades of the oncospheral hooks (HBl), surrounded by numerous long microvilli (Mv) which protrude into large cavity situated under the hook region membrane (HRM) and oncospheral membrane (OM). b Oblique section through the hook region membrane showing hook blade exit and oncospheral tegument with numerous long microvilli at its surface. DR desmosome rings, HM hook musculature, IE inner envelope
Fig. 4 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): origin, differentiation and functional ultrastructure of the oncospheral tegument and hook region membrane
Fig. 4 Consecutive stages of a tegumental perikaryon migration. a Part of an embryo in the early preoncospheral stage of development showing much infolded oncospheral membrane and the binucleate perikaryon (BSP) of the oncospheral tegument in the early stage of its migration, sunken already below the peripheral layers of oncospheral musculature. b Part of the late stage of preoncospheral differentiation showing the binucleate perikaryon of oncospheral tegument sunk deep into the central part of the embryo and surrounded by differentiating blastomeres. H oncospheral hooks, HCF hook forming cell, HRM hook region membrane, IE inner envelope, N1, N2, nucleus, OE outer envelope, OM oncospheral membrane, SC somatic cells
Fig. 3 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): origin, differentiation and functional ultrastructure of the oncospheral tegument and hook region membrane
Fig. 3 Comparison of an early and advanced preoncospheral stage of embryonic development in Echinococcus multilocularis. a Ultrastructure of an embryo in the early preoncospheral stage of embryonic development. Note the binucleate complex primordium (PBC), which appears as a syncytial cap or "calotte" situated beneath the inner envelope (IE) at one pole of the developing embryo; two thick arrows mark the direction of progressive migration of both nuclei (N1, N2) surrounded by a thin layer of common cytoplasm and become transformed into the binucleate subtegumental perikaryon. b Part of the embryo in the advanced stage of preoncosphere showing the binucleate subtegumental perikaryon (BSP) of the tegumental syncytium sunk deep into the central part of the embryo and surrounded by differentiating blastomeres. Bl blastomere, C vitelline capsule, EmB embryophoric blocks, GL granular layer, H oncospheral hooks, HM hook muscles, HRM hook region membrane, KI keratin-like protein islands, MeN mesomere nucleus, OE outer envelope, OM oncospheral membrane, PG penetration gland, UW uterine wall
Fig. 2 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): origin, differentiation and functional ultrastructure of the oncospheral tegument and hook region membrane
Fig. 2 Schematic diagram illustrating the general topography of the oncospheral tegument and hook region membrane in relation to the oncospheral hooks, penetration gland arms and glandular exits in the mature intrauterine eggs. All structures involved in formation of the oncospheral tegument and hook region membrane are marked in orange colour. BSP binucleate subtegumental perikaryon, HRM hook region membrane, IE inner envelope LH lateral hooks, MH median hooks, Mv microvilli, N1, N2 nucleus, OT oncospheral tegument, PGA penetration glands arms
Fig. 4 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): functional ultrastructure of the penetration glands and nerve cells within the oncosphere
Fig. 4 TEM micrographs of the higher magnification showing exit regions of the Echinococcus multilocularis penetration glands. a Part of the oncosphere showing the exit of the type 2 penetration gland (PG2E). Note the liquefied aspect of their secretory granules (sg2L). b Part of the hexacanth near the exit of the type 1 penetration gland (PG1E). Note the liquefied aspect of their secretory granules (sg1L). c Enlarged detail of the liquefied secretory granules of the type 1 penetration gland (sg1L). HCh heterochromatin islands, HM hook musculature, HRM hook region membrane, N nucleus, OM oncospheral membrane, PG2A arm of the type 2 penetration gland, sg2 secretory granules of the type 2 penetration gland
Fig. 5 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): functional ultrastructure of the penetration glands and nerve cells within the oncosphere
Fig. 5 Oncospheral secretory regions of the hexacanth of Echinococcus multilocularis and comparison of three types of their secretory granules. a Somatophore area of hexacanth showing few secretory regions containing three types of secretory granules: sg1, sg2, and nsg granules. Two types of penetration glands, PG1 and PG2, show evidently different types of their secretory granules sg1 and sg2. b–d Higher magnification TEM micrographs showing ultrastructural details of three types secretory granules. sg1 (or sg2) represents secretory granules of the first (or second) type of penetration glands and nsg are neurosecretory granules of neurosecretory cells. H oncospheral hook, HCh heterochromatin islands, HM hook musculature, m mitochondria, N nucleus, n nucleolus, NCP nerve cell process, OM oncospheral membrane, RA "rouleau"-shaped assemblages of secretory granules, SC somatic cell
Fig. 3 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): functional ultrastructure of the penetration glands and nerve cells within the oncosphere
Fig. 3 Enlarged details of the secretory granules sg1 in the type 1 penetration gland of Echinococcus multilocularis oncosphere and the cytochemical test of Thiéry for ultrastructural evidence of glycogen. a High power TEM micrograph showing numerous "rouleau"-shaped assemblages (RA) of the secretory granules of the type 1 penetration gland (sg1). b Cytochemical test of Thiéry showing the presence of large number of beta-glycogen particles (β-gl) around the two types of penetration glands (PG1 and PG2); results obtained after freeze substitution technique. HCh heterochromatin islands, HM hook musculature, N nucleus, OM oncospheral membrane
Fig. 6 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): functional ultrastructure of the penetration glands and nerve cells within the oncosphere
Fig. 6 TEM micrographs of the anterior, somatophore region of the oncosphere of Echinococcus multilocularis. a Pole of the hexacanth showing a bilateral symmetry. Note the presence of the arms of the type 1 penetration gland (PG1A) between the median (MH) and lateral (LH) pairs of oncospheral hooks. b Detail of an oncosphere with the peripheral disposition of a nerve cell process containing neurosecretory granules (nsg). c Enlarged detail of neurosecretory granules (nsg). H oncospheral hook, HM hook musculature, HRM hook region membrane, m mitochondria, OM oncospheral membrane, PG1 type 1 penetration gland, SM somatic musculature
Fig. 1 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): functional ultrastructure of the penetration glands and nerve cells within the oncosphere
Fig. 1 Schematic diagram illustrating localization of three secretory regions of the egg of Echinococcus multilocularis: two types of the penetration glands (PG1 and PG2) and two nerve cells (NC) of neurosecretory type. Note the oncospheral tegument composed of its peripheral anucleated layer and submerged subepithelial perikaryon and the hook region membrane surrounding the somatophore pole of the hexacanth. To simplify the diagram, some other oncospheral structures or cell types such as somatic and hook muscle systems with their
Fig. 2 in Echinococcus multilocularis (Cestoda, Cyclophyllidea, Taeniidae): functional ultrastructure of the penetration glands and nerve cells within the oncosphere
Fig. 2 Details of two infective hexacanths of Echinococcus multilocularis obtained by means of freeze substitution technique. a TEM micrograph showing the two penetration glands (PG1 and PG2) and a nerve cell (NC). Note: (i) the nucleus (N) of a nerve cell with heterochromatin islands (HCh), (ii) the presence of numerous mitochondria (m) and (iii) the neurosecretory granules (nsg) located in a nerve cell process. b Area of hexacanth with two penetration glands (PG1 and PG2). Note the "rouleau"-shaped assemblages (RA) of secretory granules of the type 1 penetration gland (sg1). H oncospheral hook, HM hook musculature, n nucleolus, OM oncospheral membrane, r ribosomes, sg2 secretory granules of the type 2 penetration gland
Figure 8. Aploparaksis xemae Schiller, 1951 in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 8. Aploparaksis xemae Schiller, 1951. Type-specimen from Xema sabini, Alaska: (A) hooks, (B) hermaphroditic proglottis, (C) cirrus. Specimen from a type-series Diorchis serpentata von Linstow, 1905 from Calidris sp. of Western Taimyr, Russia: (D) cirrus. Scale bars: 100 mm (B), 20 mm (A, C, D).
Figure 4. Aploparaksis rissae Schiller, 1951, a in Cestodes of the genus Aploparaksis Clerc, 1903 (Cyclophyllidea, Aploparaksidae) reported from gulls, with a description of new species
Figure 4. Aploparaksis rissae Schiller, 1951, a type from Rissa tridactyla, Alaska: (A) scolex, (B) hooks, (C) hermaphroditic proglottis, (D) cirrus. Scale bars: 100 mm (A, C), 50 mm, (D) 20 mm (B).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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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
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