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Fig. 9. Plectanocotyle jeanloujustinei n in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 9. Plectanocotyle jeanloujustinei n. sp. ex Chelidonichthys lastoviza from the western Mediterranean. A, Body, holotype, ventral view (HEL 1721). B, Clamp, hologenophore, ventral view (HEL 1731). C, Clamp, paratype, dorsal view (HEL 1717). D, terminal lappet, paratype (HEL 1717). E, Anterior end showing male copulatory organ, paratype, ventral view (HEL 1720). F, Egg, paratype (HEL 1714).

Fig. 4 in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 4. Tree inferred using the ML method based on the cox1 sequence data; only bootstrap values higher than 70 are indicated. The newly generated sequences of Plectanocotyle gurnardi sensu stricto are indicated in blue. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 8 in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 8. Plectanocotyle gurnardi (Van Beneden and Hesse, 1863) sensu stricto ex Eutrigla gurnardus from the North Sea, Sweden, Detail of the reproductive organs in the region of ovary, ventral view (SMNH 216584).

Fig. 5 in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 5. Tree inferred using the ML method based on the 28S rDNA sequence data; only bootstrap values higher than 70 are indicated. The newly generated sequences are indicated in bold. All sequences of Plectanocotyle gurnardi from the type-host Eutrigla gurnardus clustered in a single clade. * The polyopisthocotylean parasite annotated on GenBank as "Plectanocotyloides obscurum"; the host as "Aspitrigla obscura".

Fig. 3. Plectanocotyle jeanloujustinei n in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 3. Plectanocotyle jeanloujustinei n. sp. ex Chelidonichthys lastoviza from the western Mediterranean (Algeria), hologenophores. A-E, Body lacking only the haptor. F. Body lacking a lateral part posterior part. G-H, anterior end of the body including the male copulatory organ. The missing parts were excised and used for DNA extraction. A, (HEL1729). B, (HEL1730). C, (HEL1732). D, (HEL1733). E, (HEL1734). F, (HEL1731). G, (HEL1727). H, (HEL17287).

Fig. 2 in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 2. Plectanocotyle gurnardi (Van Beneden and Hesse, 1863) sensu stricto ex Eutrigla gurnardus from the North Sea, Sweden, hologenophores, body lacking only a lateral part; excised used for DNA extraction A, (SMNH 216644). B, (SMNH 216645). C, (SMNH 216646).

Fig. 1 in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 1. One of the unstudied specimens of Plectanocotyle gurnardi (Van Beneden and Hesse, 1863) from the type-host Eutrigla gurnardus available for study before this paper, and that hinted the presence of Plectanocotyle gurnardi in Swedish waters of the North Sea. The slide containing two specimens of Plectanocotyle gurnardi labeled as "Phyllocotyle gurnardi": unstudied specimens collected by Theodor Odhner from the gills of Eutrigla gurnardus from Kristineberg, Sweden, Northeast Atlantic.

Fig. 6 in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 6. Plectanocotyle gurnardi (Van Beneden and Hesse, 1863) sensu stricto ex Eutrigla gurnardus from the North Sea, Sweden. A, Body, ventral view (SMNH 216639). B, Clamp, ventral view (SMNH 216593). C, Anterior end showing male copulatory organ, ventral view (SMNH 216586). D, Egg, (SMNH 216594).

Fig. 7 in "Something old, something new, something borrowed, and the oioxeny is true": description of Plectanocotyle jeanloujustinei n. sp. (Polyopisthocotylea, Plectanocotylidae) from the MNHN Helminthology collection with novel molecular and morphological data for P. gurnardi (Van Beneden & Hesse, 1863) (sensu stricto) from Sweden

Fig. 7. Plectanocotyle gurnardi (Van Beneden and Hesse, 1863) sensu stricto ex Eutrigla gurnardus from the North Sea, Sweden, disposition of clamps sclerites. A, Dorsal jaw. B, Ventral jaw. C, Clamp, ventral view (SMNH 216593). 3.2. Morphology

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Fig. 2 in Remarks on Eimeria spp. (Apicomplexa: Eimeriidae) from Kobus spp. (Bovidae: Reduncini), with supplementary morphological data of Eimeria congolensis Ricci-Bitti et al., 1973 from a new host subspecies, the common waterbuck Kobus ellipsiprymnus ellipsiprymnus (Ogilbyi, 1833)

Fig. 2. Photomicrographs of sporulated oocysts of Eimeria congolensis from common waterbucks Kobus ellipsiprymnus ellipsiprymnus in a safari park of Portugal. Note the inner layer (il) and rough outer layer (rol) of the oocyst wall, micropyle (m), nucleous (n), polar granule (pg), refractile body (rb), sporocyst residuum (sr), Stieda (sb) and sub-stieda (ssb) bodies. Scale bar: 10 μm.

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Fig. 1 in Remarks on Eimeria spp. (Apicomplexa: Eimeriidae) from Kobus spp. (Bovidae: Reduncini), with supplementary morphological data of Eimeria congolensis Ricci-Bitti et al., 1973 from a new host subspecies, the common waterbuck Kobus ellipsiprymnus ellipsiprymnus (Ogilbyi, 1833)

Fig. 1. Composite line drawing of the sporulated oocyst of Eimeria congolensis from common waterbucks Kobus ellipsiprymnus ellipsiprymnus in a safari park of Portugal. Scale-bar: 10 μm.

Fig 3 in New data on the Paleocene monotreme Monotrematum sudamericanum, and the convergent evolution of triangulate molars

Fig 3. Schematic occlusal view of two left lower molars (m1–m2) of an ornithorhynchid monotreme (Obdurodon dicksoni) (A), and a pre−tribosphenic peramuran (Peramus sp.) (B). Note the difference between the "gaps" in A and the "embrasures" in B. In the former the intermolar contact results by mesial and distal cingulids. Not to scale.

Fig. 2 in New data on the Paleocene monotreme Monotrematum sudamericanum, and the convergent evolution of triangulate molars

Fig. 2. Schematic occlusal view of the advanced ornithorhynchid Obdurodon dicksoni; RM2 (A), Rm1 (B). The only know m1 of Monotrematum sudamericanum is incomplete (Fig. 1D). As both genera show similar crown pattern, we figure here the homologous teeth of O. dicksoni. Not to scale.

Fig. 1 in New data on the Paleocene monotreme Monotrematum sudamericanum, and the convergent evolution of triangulate molars

Fig. 1. Monotrematum sudamericanum RM2 (MPEF−PV 1634) in occlusal (A) and posterior (B) views. C. Base of crown showing fragment of roots. Rm1(MPEF−PV 1635); occlusal view (D), posterior view (E). F. Base of crown showing fragmentary roots. Not to scale.

Fig. 4. Monotrematum sudamericanum. A in New data on the Paleocene monotreme Monotrematum sudamericanum, and the convergent evolution of triangulate molars

Fig. 4. Monotrematum sudamericanum. A. Stereopair of RM2, occlusal view. B. Stereopair of Rm1, occlusal view. Anterior is up in A and B.

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Supplementary data for "Collision-induced absorptions by pure CO2 in the infrared: New measurements in the 1150–4500 cm−1 spectral range and empirical modeling for applications" published in Icarus. https://doi.org/10.1016/j.icarus.2024.116265

Supplementary data for the paper entitled ""Collision-induced absorptions by pure CO2 in the infrared: New measurements in the 1150–4500 cm−1 spectral range and empirical modeling for applications" published in Icarus. https://doi.org/10.1016/j.icarus.2024.116265 These data files contain the coefficients needed to compute the shape of a pure CO2 CIA band at a given temperature (see Eq. (3)) of the paper https://doi.org/10.1016/j.icarus.2024.116265 "CIA_shape_coeff.dat" involves a CIA band shape without dimer signatures  "CIA_dimer_shape_coeff.dat" involves a CIA band shape with dimer signatures  "CIA_Fermi_doublet_shape_coeff.dat" involves the Fermi doublet band shape First column is wavenumber in cm-1, the rest of the columns contain the coefficients.

FIGURE 9 in New data on Eulipotyphla (Insectivora, Mammalia) from the Late Miocene to the Middle Pleistocene of Ukraine

FIGURE 9. (1-2) cf. Asoriculus sp. from Popovo 3: 1, fragment of right mandible with coronoid process, buccal view (c.n. 29/III/9/1). 2, fragment of right mandible with m2-m3, lingual view (c.n. 29/III/9/2). (3) Neomysorex alpinoides from Verkhnya Krynitsa 2, fragment of right mandible with p4–m3, lingual view (c.n. 29/2/10/1), (4-6) Neomys newtoni from Medzhybozh: 4, left condyloid process, posterior view (c.n. 29/4/11/2); fragment of left mandible with m1–m2, in 5, lingual, and 6, occlusal view (c.n. 29/4/11/1).

FIGURE 10. 1, Beremendia fissidens from Popovo 1, right I1 in New data on Eulipotyphla (Insectivora, Mammalia) from the Late Miocene to the Middle Pleistocene of Ukraine

FIGURE 10. 1, Beremendia fissidens from Popovo 1, right I1, in anterior view (c.n. 29/I/12/1); 2, cf. Beremendia minor from Verkhnya Krynitsa 1, fragment of left mandible with proximal part of i1 in buccal view (c.n. 29/1/13/1); Petenyia dubia from Verkhnya Krynitsa 2 (3) and Lobkove (4): 3, left condyloid process, posterior view (c.n. 29/2/14/1); 4, left M1, occlusal view (c.n. 29/3/14/1). 5, Zelceina sp. from Verkhnya Krynitsa 2, fragment of left maxillae with M1-M2, occlusal view (c.n. 29/2/16/1).

FIGURE 7. 1 in New data on Eulipotyphla (Insectivora, Mammalia) from the Late Miocene to the Middle Pleistocene of Ukraine

FIGURE 7. 1, cf. Miosorex sp. from Verkhnya Krynitsa 2, right I1, buccal view (c.n. 29/2/6/1). 2, Miosorex grivensis from Popovo 3, fragment of right mandible with m2 and trigonid of m3, buccal view (c.n. 29/III/7/1).

FIGURE 4 in New data on Eulipotyphla (Insectivora, Mammalia) from the Late Miocene to the Middle Pleistocene of Ukraine

FIGURE 4. Desmana sp. from Verkhnya Krynitsa 1 (1-2) and from Popovo 2 (3-7). Left?I2, 1, buccal; 2, occlusal view (c.n. 29/1/4/1). Left C: 3, buccal; 4, occlusal view (c.n. 29/II/4/1). 5, Left P2, occlusal view (c.n. 29/II/4/2). 6, Left P4, occlusal view (c.n. 29/II/4/3). 7, Right M1, occlusal view (c.n. 29/II/4/4).