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Figure 1. – A in First steps towards Live-action Virtual Reality Games

Figure 1. – A: The Clipperton-La Passion Island (France) lies in the NorthEastern Tropical Ocean at a minimum distance of 945 km from the first emerged ground constituted by Socorro Island in the Mexican Exclusive Economic Zone. The closest potential sources for the colonization are Marquesas (French Polynesia) on the Eastern side and Galapagos (Ecuador) on the Western side, respectively (map modified from "Carte de l'île de la Passion", 2004, by C. Jost); B: Approximative location of the adult Caranx ignobilis identified on the 4 February 2016 (+ represent the location of the six dives).

Figure 2 in First steps towards Live-action Virtual Reality Games

Figure 2. – Photography of an adult individual of Caranx ignobilis on the eastern side reef slope of the Clipperton atoll on the 4 February 2016. The dorsal profile of steep and nearly straight snout, plus the silvery gray dorsal colour, shading to silvery white ventrally, with numerous scattered, very small black spots, are quite characteristic of this species of jack (Photo E. Clua).

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Fig. 1 in Sarcocystis cruzi infection in free-living European bison (Bison bonasus bonasus L.) from the Białowieza˙Forest, Poland - A molecular analysis based on the cox1 gene

Fig. 1. Overview of consistent nucleotide differences between two cox1 gene sequences of S. cruzi MW490605 and MW490606. Numbers above and below the sequences refer to nucleotide positions in the two GenBank sequences used in the comparison. Positions where the two sequences were identical are signified with Dots (.).

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Fig. 2 in Sarcocystis cruzi infection in free-living European bison (Bison bonasus bonasus L.) from the Białowieza˙Forest, Poland - A molecular analysis based on the cox1 gene

Fig. 2. Phylogenetic tree for selected Sarcocystis cruzi isolates and selected members of Sarcocystis species found in Bovidae based on partial sequences of cox1 using the maximum parsimony method. The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1000 replicates) are shown next to the branches. GenBank accession numbers are listed next to the taxon names. The country of origin of S. cruzi isolates are listed in brackets.

Fig. 3 in A new Eocene free-living cheyletid mite from Baltic amber

Fig. 3. Cheyletid mite Cheletomimus crinitus sp. nov., female holotype (SMF Be 2537, ex. CCHH 448-1) from Baltic amber (Baltic Sea coast, most likely Sambian Peninsula, middle to upper Eocene, 37–54.5 Mya). A. Dorsal view of gnathosoma and anterior opisthosoma (micropanorama assembled from ca 80 images). B. Detail of left palp in ventral view (assembled from 18 images). C. Posterior of ano-genital area in lateral antiaxial view in lateral antiaxial view (assembled from ca. 40 images). D. Left leg I tarsus in lateral antiaxial view (from 22 focal planes). Note extremely poor visibility of seta p′′ against the background of the leg. Abbreviations: a, antelateral seta; acm, anteroculminal palpal eupathidia; ag1–3, aggenital setae, b.s., bush-like seta; d, dorsal seta; elc, supracoxal seta; emp, empodium; F, femur; ft, fastigial seta; G, genu; g1–2, genital setae; h3, seta of segment H; l, lateral seta; oc, ocellus; p , proral seta; per, peritreme; ps1–3, pseudanal setae; tc, tectal seta; Ti, tibia; ti.cl, tibial claw; u, unguinal seta; ul, ultimal palpal eupathidium; ve, vertical external prodorsal s4eta; vi, vertical internal prodorsal seta; vs, ventrosagittal seta; ω, tarsal solenidion; ′ and ′′ refer to position of seta in pseudosymmetrical pair on appendage: anterior or posterior, respectively.

Fig. 2 in A new Eocene free-living cheyletid mite from Baltic amber

Fig. 2. Cheyletid mite Cheletomimus crinitus sp. nov., female holotype (SMF Be 2537, ex. CCHH 448-1) from Baltic amber (Baltic Sea coast, most likely Sambian Peninsula, middle to upper Eocene, 37–54.5 Mya), brightfield layered micropanaramas, each combined from ca. 170 focal planes. Dorsal (A) and ventral (B) views. Abbreviations: 1a–c, 2c, 3a–c, 4a–c, coxal setae of coxae 1–4, respectively; ag1, anterior aggenital seta; c2, d2, e2, f2, h1–h3, dorsal setae, associated with body segments C, D, E, F, H, respectively; oc, ocellus; se, scapular external prodorsal seta; si, scapular internal prodorsal seta; ve, vertical external prodorsal seta; vi, vertical internal prodorsal seta.

Fig. 1 in A new Eocene free-living cheyletid mite from Baltic amber

Fig. 1. Cheyletid mite Cheletomimus crinitus sp. nov., female holotype (SMF Be 2537, ex. CCHH 448-1) from Baltic amber (Baltic Sea coast, most likely Sambian Peninsula, middle to upper Eocene, 37–54.5 Mya), reconstruction (leg positions altered for clarity). Dorsal (B) and ventral (C) views, right palp A) and left tibia and tarsus I (D) in dorsal views, left tarsus I in ventral view (E). Abbreviations: 1a–c, 2c, 3a–c, 4a–c, coxal setae of coxae 1–4, respectively; c2, d2, e2, f2, h1–h3, dorsal setae, associated with body segments C, D, E, F, H, respectively; ′ and ′′ refer to position of seta in pseudosymmetrical pair on appendage: anterior or posterior, respectively.

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Fig. 2 in A Late Miocene potential neobalaenine mandible from Argentina sheds light on the origins of the living pygmy right whale

Fig. 2. Left mandible of a fossil neobalaenine baleen whale, gen. et. sp. indet. (MPEF-PV2572) from Punta Ninfas, Chubut Province, Argentina; Puerto Madryn Formation (Late Miocene), showing the mandibular condyle as preserved in the field prior to excavation.

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Fig. 1 in A Late Miocene potential neobalaenine mandible from Argentina sheds light on the origins of the living pygmy right whale

Fig. 1. Left mandible of a fossil neobalaenine baleen whale, gen. et sp. indet. (MPEF-PV2572) from Punta Ninfas Chubut Province, Argentina; Puerto Madryn Formation (Late Miocene). A. Lateral view. B. Medial view. C. Medial view of the posterior region of the mandible showing the morphology of the coronoid process. D. Dorsal view of the mandible showing the lateral curvature of the body. E. Anteromedial view of the mandible showing the medial torsion of the anteriormost portion of the body.

Fig. 9 in Live-live and live-dead interactions in marine death assemblages: The case of the Patagonian clam Venus antiqua

Fig. 9. Orientation of Venus antiqua King, 1832 in various situations. A. Reclining or reworked orientation. B. Erect probing orientation. C. Infaunal orientation. D. Semi-infaunal orientation.

Fig. 7 in Live-live and live-dead interactions in marine death assemblages: The case of the Patagonian clam Venus antiqua

Fig. 7. Comparison between observed and expected frequencies of Crepidula spp. encrustations on Venus antiqua King, 1832 shells from Bustamante Bay.

Fig. 6 in Live-live and live-dead interactions in marine death assemblages: The case of the Patagonian clam Venus antiqua

Fig. 6. Different types of damage recorded in modern Trophon geversianus shells collected from the same samples that the Venus antiqua King, 1832 shells, Bahía Bustamante. A. Shell with predatory drill hole. B. Intact shell. C. Shell with damage to shell aperture margin. D. Shell with crack in body whorl. E. Shell with a major damage in last whorl. F. Shell with columella damage. Pie charts show the proportion of snails (N = 34) with each type of damage, used here to infer crushing and drilling predation. Scale bars 10 mm.

Fig. 5 in Live-live and live-dead interactions in marine death assemblages: The case of the Patagonian clam Venus antiqua

Fig. 5. Shell size frequency distribution of drilled (white bars) and undrilled (black bars) modern Venus antiqua King, 1832 shells. A. Shell length. B. Shell height. C. Geometric mean of shell length and height.

Fig. 4 in Live-live and live-dead interactions in marine death assemblages: The case of the Patagonian clam Venus antiqua

Fig. 4. Marks of epibionts on Venus antiqua King, 1832 shells, Recent, Bahía Bustamante. A. CEGH-UNC 25333, external view of a right valve with a mark that reproduces the basal outline shape of Crepidula. The central dark zone reproduces the rounded muscular foot of Crepidula. B. CEGH-UNC 25334, internal view of a right valve covered with calcareous tubes of tubiculous polychaetes. This figure also shows hinge ligament remains. Scale bars 10 mm.

Fig. 8 in Live-live and live-dead interactions in marine death assemblages: The case of the Patagonian clam Venus antiqua

Fig. 8. Bar charts showing proportion of modern Venus antiqua King, 1832 shells exhibing two different biotic interactions.

Fig. 1 in Live-live and live-dead interactions in marine death assemblages: The case of the Patagonian clam Venus antiqua

Fig. 1. Scheme showing biotic interactions (live/live interactions) and postmortem encrustation (live/dead interactions) associated with Venus antiqua King, 1832 shells preserved in molluscan death assemblages.

Fig. 3 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 3. Boxplot of tick abundance, female-to-male ratio and important climate factors change by months. A: Tick daily abundance; B: Daily female-to-male ratio of ticks; C: Daily temperature; D: Daily air pressure. Variables sharing the same letters among months were not significantly different. The five-day-rolling average values were calculated for all the variables that change by months.

Fig. 6 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 6. Daily average tick abundance, daily average air pressure and daily average temperature with standard deviations by months. All the values are calculated with five-day-rolling average values.

Fig. 2. Ixodes. ovatus collected from the giant panda. A in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 2. Ixodes. ovatus collected from the giant panda. A: Dorsal of the adult female I. ovatus; B: Ventral of the adult female I. ovatus; C: Dorsal of the adult male I. ovatus; D: Ventral of the adult male I. ovatus.

Fig. 5 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 5. The correlation plot of daily tick abundance and the daily air pressure with trending line. The five-day-rolling average values were calculated for tick abundance and the air pressure.