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Fig. 2 in Cerebral cysticercosis in a wild Bengal tiger (Panthera tigris tigris) in Bhutan: A first report in non-domestic felids

Fig. 2. Cysts identified at necropsy of the Bengal tiger in Bhutan (left) and isolated in a jar (right).

opencc-by-4.0Aug 2021View details →

Fig. 1 in First report of Trichinella pseudospiralis in a wolf (Canis lupus italicus)

Fig. 1. Map of Italy with Trichinella pseudospiralis records. Black circle, T. pseudospiralis in hunted wild boar; open circle, T. pseudospiralis in farmed wild boar; striped circle, T. pseudospiralis human outbreak caused by wild boar meat; black triangle, T. pseudospiralis in hunted red fox; black square, T. pseudospiralis and Trichinella britovi in a wolf; black star, T. pseudospiralis in night bird of prey; open star, T. pseudospiralis in a red kite. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Apr 2021View details →

Fig. 3 in Cerebral cysticercosis in a wild Bengal tiger (Panthera tigris tigris) in Bhutan: A first report in non-domestic felids

Fig. 3. Cladogram showing the relation between the sequences of the cox1 gene of Taenia solium from the present study highlighted in bold (MT366763- MT366764) and unique published sequences of the cox1 gene available in GenBank from Tanzania (TANZ), Brazil (BRA), Mexico (MEX), Ecuador (ECU), Madagascar (MDG), Indonesia (INDO- PA, INDO-BA), China (CHI), Nepal (NEP), Thailand (THA) and India (TAE). Sequences for the cox1 gene from Taenia saginata (AB066495) and T. asiatica (AB066494) were also included. The cox1 sequence of Echinococcus multilocularis (MN251845) was used as an outgroup.

opencc-by-4.0Dec 2022View details →

Figs 1-4. 1 in First report of a nest of Ceratina (Ceratinula) fioreseana Oliveira (Hymenoptera: Apidae)

Figs 1-4. 1, Dry petiole of Cecropia pachystachya used as nesting substrate by a female of Ceratina fioreseana; 2, living female found in the nest; 3, emerging female; 4, polar view of Emilia fosbergii pollen grain. Figs 2, 3, Scale bars: 2 mm; 4, Scale bar: 50 μm.

Fig. 8 in The first report of South American edrioasteroids and the paleoecology and ontogeny of rhenopyrgid echinoderms

Fig. 8. Lateral CD ambulacral view of holotype PIL 14656−H of Rhenopyrgus piojoensis sp. nov., Silurian (lower Ludlow), Los Espejos Formation, Argentina, showing the notch in the collar plates and the small irregular plates leading to the perirpoctal area. Note that floor plates are exposed in the distal ambulacra and the anal pyramid lies along the edge of the integrated interradial plate at the top of the periproctal notch.

Fig. 5 in The first report of South American edrioasteroids and the paleoecology and ontogeny of rhenopyrgid echinoderms

Fig. 5. Comparison of Ludlow conodont zones between Europe, North America, Asia, and the Precordillera.

Fig. 4 in The first report of South American edrioasteroids and the paleoecology and ontogeny of rhenopyrgid echinoderms

Fig. 4. Scanning electron micrographs of conodont elements documenting the Silurian (lower Ludlow) age of the Los Espejos Formation. All figured elements were collected from the Los Espejos Formation of the Precordillera. A, D. Kockelella variabilis variabilis Walliser, 1957. A. P element, upper view, sample 7, CML−C 3067 (1). D. S element, posterior view, sample 3, CML−C 3058 (2). B, H. Ozarkodina excavata excavata (Branson and Mehl, 1933). B. Pb element, lateral view, sample 3, CML−C 3057 (6). H. S element, lateral view, sample3, CML−C 3057 (7). C. Corysognathus dubius (Rhodes, 1953); Pb element, posterior lateral view, sample 3, CML−C 3055 (4). E. Oulodus siluricus (Branson and Mehl, 1933); Pb element, lateral view, sample 3, CML−C 3052 (4). F. Pseudooneotodus beckmanni (Bischoff and Sannemann, 1958); lateral view, samples 3, CML−C 3054 (5). G. Ozarkodina confluens (Branson and Mehl, 1933); Pb element, lateral view, sample 3, CML−C 3071 (1). Scale bars 0.1 mm.

Fig. 2 in The first report of South American edrioasteroids and the paleoecology and ontogeny of rhenopyrgid echinoderms

Fig. 2. Trees showing the phylogenetic position of rhenopyrgids with respect to other edrioasteroid clades. A. Strict consensus of the two, equally most parsimonious trees of 18 evolutionary steps. Numbers at nodes are the bootstrap and decay index for these nodes. B. Single most parsimonious tree of 26 steps recovered when the search was constrained to retain only those trees that placed Rhenopyrgus Dehm, 1961 as sister taxon to the pyrgocystid Argodiscus Prokop, 1965. Note that except for the placement of Rhenopyrgus, the trees are congruent.

Fig. 1 in The first report of South American edrioasteroids and the paleoecology and ontogeny of rhenopyrgid echinoderms

Fig. 1. Rhenopyrgids and Pyrgocystis showing the superficial similarity in the construction of the theca. A. Paratype NHM−E−16237 of Rhenopyrgus? ansticei (Bather, 1915) in lateral view; Wenlock Shale, Silurian, UK. B. Holotype NHM−E−16232 of Pyrgocystis sardesoni Bather, 1915; Decorah Shale (Ordovician) Minnesota, USA. Oral view showing the oral surface covered with small spines (B1) and lateral view showing the extensive, disorganized pedunculate zone (B2). C. NHM−E−62753 Rhenopyrgus? procera (Aurivillius, 1892); Silurian, UK. Part (C1) and counterpart (C2) showing the well−developed pedunculate of this complete specimen. Note that the oral surface is extremely poorly preserved. D. Holotype NHM−E−23470 of Pyrgocystis grayae (Bather, 1915); Drummuck Series, Ordovician, Scotland. Lateral summit detail (D1), lateral A ambulacral (D2) and summit (D3) views. E, F, G. Rhenopyrgus whitei Holloway and Jell, 1983, Humevale Formation, Silurian, Australia. E. Lateral view of distal pedunculate zone of paratype NMV P−67681. F. Lateral summit view of holotype NMV P−67680a. G. Lateral view of paratype NMV P−67682 showing both proximal and distal portions of the theca. Scale bars 2.5 mm.

Fig. 7 in The first report of South American edrioasteroids and the paleoecology and ontogeny of rhenopyrgid echinoderms

Fig. 7. Size and orientation of rhenopyrgids. A. Rose diagram showing the orientation of theca on slab surface. Vector is measured as the angle between a randomly assigned "north" arrow and the projection of the oral surface of the extended theca. B. Width of the proximal portion of the pedunculate zone. Note the normal distribution of thecal size.

opencc-by-4.0Mar 2009View details →

Fig. 1 in First report on the occurrence of Neseuretinus and Ovalocephalus trilobites in the Middle Ordovician of Iran

Fig. 1. Geographical map (A) showing the position of fossil locality in the Derenjal Mountains north of Tabas and stratigraphical column (B) through Section B in the upper part of the Shirgesht Formation, showing stratigraphical ranges of selected trilobite, ostracod, and conodont species (after Ghobadi Pour et al. 2006). The dashed line for Neseuretinus birmanicus indicates the position of specimens collected lose on the surface and therefore only in approximate stratigraphical position.

opencc-by-4.0Dec 2018View details →

Figure 1 in First reported predation of fledgling Micronesian starlings (Aplonis opaca) by brown treesnakes (Boiga irregularis) on Guam

Figure 1. Photo of BTS (11-Aug-17) necropsy showing A) Micronesian starling fledgling carcass being excised and B) a fledgling carcass with color bands. Photos taken by M. Kastner.

opencc-by-4.0Jun 2022View details →

Figure 1 in First report of Xiphinema ifacolum Luc, 1961 (Dorylaimida: Longidoridae) from Nigeria

Figure 1: Light micrographs of Xiphinema ifaCOlUm Luc, 1961 from Nigeria (A–I). (A) Whole female, (B,C) Female lip region showing amphidial fovea, (D–G) Detail of Z-organ in uterus, (H–I) Female tail regions. IndiCatOrS: af = amphidial fovea; a = anus; Zorg = Z-organ. (Scale bars: A = 200 µm; B, C, G–I = 10 µm; D–F = 20 µm).

opencc-by-4.0Mar 2020View details →

Figure 1 in First report of Bursaphelenchus fungivorus (Nematoda: Aphelenchida) in Italy and an overview of nematodes associated with Crocus sativus L.

Figure 1: Light micrographs of BUrSaphelenChUS fUngiVOrUS. A: Male total body; B: Female anterior region; C: Female tail; D: Vulval region; E: Lateral view of male tail; F: Ventral view of male tail (Scale bar A = 100 µm; B-F = 20µ m).

opencc-by-4.0Mar 2020View details →

Figure 2 in First report of Bursaphelenchus fungivorus (Nematoda: Aphelenchida) in Italy and an overview of nematodes associated with Crocus sativus L.

Figure 2: Phylogenetic relationships of species belonging to fUngiVOrUS-group based on ITS locus. The tree was inferred using GTR + I + G as nucleotide substitution model, tested with 1,000 bootstrap replicates and BUrSaphelenChUS COCOphilUS was chosen as outgroup species. Nodes were annotated with NJ and ML bootstrap values, respectively.

Fig. 2 in First report of a member of the family Mermithidae parasitizing the sandhopper Orchestoidea tuberculata (Amphipoda, Talitridae) in Chile

Fig. 2. Genealogical relationships of haplotypes based on partial sequences of the mitochondrial cytochrome oxidase I (COI) (A) and 18S ribosomal DNA (B) gene sequences of specimens of the family Mermithidae recovered in a Bayesian inference analysis. Numbers next to nodes refer to support values. Bayesian posterior probability values are shown left of the diagonal. Bootstrap support values found in the Maximum Likelihood analysis are shown right of the diagonal. Accession numbers from GenBank are included in the terminal labels. Sequences in red were generated in this study. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in First report of a member of the family Mermithidae parasitizing the sandhopper Orchestoidea tuberculata (Amphipoda, Talitridae) in Chile

Fig. 1. The mermithid nematode and the host Orchestoidea tuberculata sampled in this study. A. Ventral view of Orchestoidea tuberculata parasitized by a juvenile mermithid. B. Head of the nematode, C. Tail showing straight spur of the nematode.

Fig. 1. Liver showing a in First report of infection with metacestode stages of Echinococcus multilocularis in a kulan (Equus hemionus kulan) from Slovakia

Fig. 1. Liver showing a single nodular encapsulated mass of about 6 cm in diameter. The mainly solid cut surface reveals several small cystic areas (arrows).

Fig. 3 in First report of infection with metacestode stages of Echinococcus multilocularis in a kulan (Equus hemionus kulan) from Slovakia

Fig. 3. Phylogenetic analysis of the herein obtained sequence (Donkey_Slovakia) and exemplary sequences from GenBank (e.g., OK268248.1; OP277525.1) using the Neighbor-Joining method, bootstraps consensus tree inferred from 1000 replicates. A sequence of E. granulosus was used as an outgroup (OR166778.1).

Fig. 2 in First report of infection with metacestode stages of Echinococcus multilocularis in a kulan (Equus hemionus kulan) from Slovakia

Fig. 2. Photomicrograph of the hepatic nodular lesion showing a pyogranulomatous to necrotizing inflammation with intralesional fragments of amorphous band-like eosinophil and strongly PAS-positive (inset) structures, consistent with the laminated layer of the larval stage of Echinococcus multilocularis. Hematoxylin-eosin stain and Periodic acid-Schiff stain (inset), respectively.