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Fig. 7 in First Mesozoic record of the stingray Myliobatis wurnoensis from Mali and a phylogenetic analysis of Myliobatidae incorporating dental characters

Fig. 7. Comparative extant taxa of Myliobatidae. A, B, D. Articulated jaws and tooth rows. C. Disarticulated jaws and articulated tooth rows. E–G. Articulated tooth rows. A. Raja sp., AMNH 92321b, in labial view. B. Dasyatis sp., FMNH 15625, in labial view. C. Rhinoptera quadriloba (LeSueur, 1817), FMNH 82986, in occlusal view. D. Myliobatis californica Gill, 1865, MCZ 424, in lingual view. E. Mobula hypostoma (Bancroft, 1831), AMNH 44124, in occlusal view, photograph (E1), line drawing (E2); F. Mobula rochebruni (Vaillant, 1879), FMNH 38450, in occlusal view, photograph (F1), line drawing (F2). G. Manta hamiltoni (Walbaum, 1792), FMNH 41385, in occlusal view, photograph (G1), line drawing (G2). H. Aetobatus narinari (Euphrasen, 1790), FMNH 10985, in labial view.

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Fig. 5 in Identification and phylogenetic analysis of Taenia spp. parasites found in wildlife in the Emilia-Romagna region, northern Italy (2017-2022)

Fig. 5. Geographical location of animals resulted positive for Taenia spp. Icons placed around circles are located in the same position, represented by the yellow point. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

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Fig. 1 in Identification and phylogenetic analysis of Taenia spp. parasites found in wildlife in the Emilia-Romagna region, northern Italy (2017-2022)

Fig. 1. Schematic representation of Taenia spp. life cycle in wildlife with accidental involvement of humans as intermediate hosts. Animals images taken from www. phylopic.org (Authors: Tracy Heath, Ferran Sayol, Anthony Caravaggi, Katy Lawler). The Figure was partly generated using Servier Medical Art, provided by Servier, licensed under a Creative Commons Attribution 3.0 unported license.

opencc-by-4.0Dec 2023View details →

Fig. 6 in Identification and phylogenetic analysis of Taenia spp. parasites found in wildlife in the Emilia-Romagna region, northern Italy (2017-2022)

Fig. 6. Phylogenetic tree with the sequences of small ribosomal RNA subunit (rrnS) of T.hydatigena (yellow), T. serialis (orange), T. pisiformis (magenta), T. crassiceps (purple) sequenced at the IZSLER, compared with public sequences deposited in Gen- Bank (black). The tree was obtained using the HKJ + G substitution model. Chain length = 10 million iterations. Node labels are posterior probabilities ≥0.9. Squares = sequence from intermediate host; circles = sequence from definitive host. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 9 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae

Fig. 9. The strict consensus of the five most parsimonious trees of Dyrosauridae found based on a cladistic analysis of 13 taxa and 30 characters (Appendices 1 and 2), and historical biogeography. Tree length: 44 steps long (C.I. excluding uninformative characters: 0.66; R.I.: 0.85; R.C.: 0.62). Land area abbreviations in the circles indicate optimised transformations on the tree, with two alternative results in light grey, and dark grey. Abbreviations: C, Congo; NAf, North Africa; NAm, North America; WAf, West Africa.

Fig. 8 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae

Fig. 8. Arambourgisuchus khouribgaensis gen. et sp. nov., Sidi Chenane, Morocco, late Palaeocene. Elements of mandibles. A. OCP DEK−GE 1200 in ventral view. B. OCP DEK−GE 269 in dorsal (B1) and lateral (B2) views. The arrows indicate the teeth that have been added recently, and which do not belong to the same specimen.

Fig. 5 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae

Fig. 5. Arambourgisuchus khouribgaensis gen. et sp. nov., OCP DEK−GE 300, Sidi Chenane, Morocco, late Palaeocene, detail of the right posttemporal fenestra in posterior view. Photograph (A) and explanatory drawing of the same (B).

Fig. 4 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae

Fig. 4. Arambourgisuchus khouribgaensis gen. et sp. nov., reconstruction of skull in dorsal (A) and ventral (B) views.

Fig. 6 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae

Fig. 6. Arambourgisuchus khouribgaensis gen. et sp. nov., OCP DEKGE 300, Sidi Chenane, Morocco, late Palaeocene, skull in occipital view. Photograph (A) and explanatory drawing of the same (B).

Fig. 3 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae

Fig. 3. Arambourgisuchus khouribgaensis gen. et sp. nov., OCP DEK−GE 18, Sidi Chenane, Morocco, late Palaeocene, skull and mandible in dorsal view. Photograph (A) and explanatory drawing of the same (B).

Fig. 1 in A new dyrosaurid crocodyliform from the Palaeocene of Morocco and a phylogenetic analysis of Dyrosauridae

Fig. 1. Geographical position of the type locality. A. Geographical position of the Ouled Abdoun Basin (Morocco) in the Palaeocene deposit of Africa, (shaded area); modified from Capetta (1972). B. Simplified geological map of the Ouled Abdoun Basin; Sidi Chenane is the type locality (modified from Salvan 1952).

Figure 11 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 11. - The asymmetric liver of an angler, Lophius piscatorius, dorsal view. l.h.l.: left hepatic lobe; r.h.l.: right hepatic lobe. The black arrow indicates the anterior part of the specimen. Scale = 50 mm.

Figure 12 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 12. - Schematic distribution of the supramedulary neurons among teleostean fishes [modified from Mola and Cuoghi (2004)]. A: Type I present in Salmonidae, Syngnathidae, Cottidae, Labridae, Percidae and some Pleuronectiformes; B: Type II present in Lophiiformes, Tetraodontiformes and Batrachoidiformes. Legend: 1: spinal cord; 2: central canal; 3: supramedulary neurons. The black arrow indicates the anterior part of the spinal cord.

Figure 10 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 10. - The central nervous system of an angler (SL = 28.8 cm), Lophius piscatorius, dorsal view. cr.n.: cranial nerves; e.: encephalon; f.t.: filum terminale; op.n.: optic nerves; s.c.: spinal cord. The black arrow indicates the anterior part of the specimen. Scale = 50 mm.

Figure 7 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 7. - The thyroid gland of an angler, Lophius piscatorius, right lateral view. ly.v: lymphatic vessels; th.a: thyroidian artery; th.s: thyroidian sinus. The black arrow indicates the anterior part of the specimen. Scale = 3 mm.

Figure 8 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 8. - Horizontal section in the thyroid gland of an ocean sunfish, Mola mola, ventral view. c.b.v: cut blood vessels; th.t: thyroidian tissue. The black arrow indicates the anterior part of the specimen. Scale = 30 mm.

Figure 9 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 9. - Parasagittal section on a frozen specimen of a black seabream, Spondyliosoma cantharus, left lateral view. k: kidney; ov: ovary; sb: swimbladder; s.c: spinal cord. The black arrow indicates the anterior part of the specimen. Scale = 20 mm.

Figure 6 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 6. - Sagittal section of a frozen of a black seabream, Spondyliosoma cantharus, left lateral view. b.cav: buccal cavity; e: encephalon; s.c: spinal cord; th.i: thyroidian islets; v: ventricle. The black arrow indicates the anterior part of the specimen. Scale = 10 mm.

Figure 5 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 5. - Visceral anatomy of a Buntal puffer, Tetraodon palembangensis, ventral view. The swimbladder and the digestive tract have been put away. ab.cav: abdominal cavity; c.oe: cut oesophagus; c.pc: cut pericardium; k: kidneys; v: ventricle. The black arrow indicates the anterior part of the specimen. Scale = 10 mm.

Figure 4 in Evidence for a close phylogenetic relationship between the teleost orders Tetraodontiformes and Lophiiformes based on an analysis of soft anatomy

Figure 4. - Visceral anatomy of an angler, Lophius piscatorius, ventral view. The digestive tract has been put away. ab.cav: abdominal cavity; c.oe: cut oesophagus; k: kidneys; v: ventricle. The black arrow indicates the anterior part of the specimen. Scale = 10 mm.