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Fig. 7 in First description of Onchocerca jakutensis (Nematoda: Filarioidea) in red deer (Cervus elaphus) in Switzerland

Fig. 7. Microfilaria showing transverse annulation and irregular shape of swollen anterior end (magnitude of annulation and swelling might be exaggerated by artefact of fixation).

Fig. 5 in First description of Onchocerca jakutensis (Nematoda: Filarioidea) in red deer (Cervus elaphus) in Switzerland

Fig. 5. External cuticular annulation (A) of O. jakutensis female with interruption over lateral field.

Fig. 4. a and b in First description of Onchocerca jakutensis (Nematoda: Filarioidea) in red deer (Cervus elaphus) in Switzerland

Fig. 4. a and b: Posterior end of O. jakutensis male with 5 pairs of pericloacal papillae without unpaired precloacal papilla.

Fig. 3. O in First description of Onchocerca jakutensis (Nematoda: Filarioidea) in red deer (Cervus elaphus) in Switzerland

Fig. 3. O. jakutensis male and female (bars: 100 Mm): a. Tail of male with five pairs of pericloacal and two pair of closely spaced terminal papillae. b. Tail of another male with more distantly spaced papillae on tail end. Left spicule protruding. c. Spicules in ventral view. d. Head end of male. e. Head end of female with vulva. f. Posterior end of female with conical tail in ventral view, annulations indicated on sides. g. Microfilaria with terminal distribution of nuclei.

Fig. 1 in First description of Onchocerca jakutensis (Nematoda: Filarioidea) in red deer (Cervus elaphus) in Switzerland

Fig. 1. Subcutaneous nodule in red deer skin with partly freed O. jakutensis female (stained with methylene blue). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

opencc-by-4.0Dec 2017View details →

Fig. 1. Subcutaneous nodules. a in Nodular onchocercosis in red deer (Cervus elaphus) in Sweden

Fig. 1. Subcutaneous nodules. a) in the subcutaneous fascia from the rump of a carcass b) parts of the threadlike O. flexuosa extracted from a subcutaneous nodule.

opencc-by-4.0Apr 2019View details →

Fig. 1 in Prevalence and co-infection with tick-borne Anaplasma phagocytophilum and Babesia spp. in red deer (Cervus elaphus) and roe deer (Capreolus capreolus) in Southern Norway

Fig. 1. Phylogenetic tree of Babesia isolates and samples of this study (●), based on fragments of 18S rRNA, generated using the Maximum-Likelihood clustering method in MEGA 6 software (1000 replicates; bootstrap values indicated at the nodes). Abbreviations: AU - Austria, BE - Belgium, CA - Canada, DE - Germany, FR - France, HU - Hungary, IT - Italy, JP - Japan, LT - Lithuania, NO - Norway, PL - Poland, RU - Russia, SK - Slovakia, SP - Spain, TU - Turkey, US - United States.

opencc-by-4.0Dec 2019View details →

Fig. 2 in Morphological and molecular characteristics of seven Sarcocystis species from sika deer (Cervus nippon centralis) in Japan, including three new species

Fig. 2. Light microscopic appearance of sarcocysts isolated from sika deer from Gifu Prefecture, Central Japan. a-d Thumb-like (a, b) and elongated finger-like (c, d) protrusions (P) of S. japonica. e, f Finger-like protrusions in S. cf. tarandi (e) and S. matsuoae (f). g, h Hair-like protrusions in S. pilosa (g) and S. gjerdei (h). i Indistinct protrusions on cyst S. cf. taeniata. j, k Oval sarcocyst of S. ovalis (j); cyst surrounded by fibrous layer (FL), making the slanting tongue-like protrusions (arrow) nearly invisible (k).

opencc-by-4.0Dec 2019View details →

Fig. 1 in Morphological and molecular characteristics of seven Sarcocystis species from sika deer (Cervus nippon centralis) in Japan, including three new species

Fig. 1. Phylogenetic tree based on 322 partial sequences of cox1 of 61 taxa, including the seven Sarcocystis species (types 1–7) from this study and inferred using the neighbour-joining method and with evolutionary distances computed using the p-distance method. Bootstrap support (1000 replicates) is shown at each node. Subtrees formed by two or more haplotypes of the same species have been collapsed. The number of haplotypes included is given in parentheses. The number of sequences of each Sarcocystis species used in this analysis and their GenBank accession numbers are shown in Table S3.

opencc-by-4.0Apr 2020View details →

Fig. 2 in Effects of introduced sika deer (Cervus nippon) and population control activity on the distribution of Haemaphysalis ticks in an island environment

Fig. 2. Seasonal changes in tick abundance of the dominant species (A) H. megaspinosa, (B) H. longicornis, and (C) H. cornigera on Niijima Island. (Broken line with black dot: Larvae, Dotted-dashes line with back triangles: Nymphs, Solid line with crosses: Adults).

opencc-by-4.0Apr 2020View details →

Fig. 3 in Effects of introduced sika deer (Cervus nippon) and population control activity on the distribution of Haemaphysalis ticks in an island environment

Fig. 3. Statistical summary of the abundances of H. megaspinosa larvae. (A) Days since the last sika deer was captured in August–November, (B) days since the last sika deer was captured in August–November for the high sika deer group, and (C) days since the last sika deer was captured in August–November for the low sika deer group. (X mark inside box: mean, lower and upper side of the box: first and third quartiles, line inside box: median, lower and upper error lines 10th and 90th percentiles, respectively, circles: data falling outside 10th and 90th percentiles).

opencc-by-4.0Apr 2020View details →

Fig. 1 in Effects of introduced sika deer (Cervus nippon) and population control activity on the distribution of Haemaphysalis ticks in an island environment

Fig. 1. Map of Niijima Island, with locations of foot snare traps (black circle), and tick collection routes for the tick survey conducted June, August, and November of 2018 and February of 2019 (orange area). (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. 2 in Identification of Anaplasma spp. in Tian Shan wapiti deer (Cervus elaphus songaricus) in Xinjiang, China

Fig. 2. Phylogenetic tree of A. phagocytophilum based on the 16S rRNA partial gene sequences. A neighbor-joining tree was constructed using the Kimura two-parameter model in the Mega 5.1 software. An alignment of 641 bp partial 16S rRNA sequence was used to construct this tree. Numbers on the branches indicate the percent of replicates that reproduced the topology for each clade. Gray square indicates sequences obtained from the study.

opencc-by-4.0Apr 2021View details →

Fig. 1 in Identification of Anaplasma spp. in Tian Shan wapiti deer (Cervus elaphus songaricus) in Xinjiang, China

Fig. 1. Phylogenetic tree of A. ovis based on the msp4 partial gene sequences. A neighbor-joining tree was constructed using the Kimura two-parameter model in the Mega 5.1 software. An alignment of 584 bp partial msp4 gene sequences was used to construct this tree. Numbers on the branches indicate the percent of replicates that reproduced the topology for each clade. Gray square indicates sequences obtained from the study.

Fig. 8 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 8. Morphological features distinguishing the distal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B), in anterior (A1, B1), distal (A2,B2), and posterior (A3,B3) views (modified from Breda 2005).

Fig. 7 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 7. Morphological features distinguishing the proximal portion of the humerus of Rangifer tarandus (A) and Cervus elaphus (B) (modified from Pales and García 1981).

Fig. 6 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 6. Scatterplots of different combinations of scapular measurements and indices for Rangifer tarandus and Cervus elaphus from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene. Abbreviations: GLP, greatest anteroposterior length of the glenoid process; LG, greatest anteroposterior length of the glenoid cavity; SLC, minimum diameter of the scapular neck.

Fig. 3 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 3. Osteological measurements of the scapula (A, B) and the humerus (C, D) (modified from Weinstock 2000a). All drawings are based on Rangifer tarandus.

Fig. 4 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 4. Morphological features distinguishing the scapulae of the cervid mammals Rangifer tarandus, BGG KI-IX.2D.39.618 (A) and Cervus elaphus, BGG KI-IX.2C.28.142 (B), from Kiputz IX (southern Pyrenees, Spain), Late Pleistocene, in lateral (A 1, B 1) and distal (A 2, B 2) views; α, the angle formed by the glenoid cavity and the supraglenoid tubercle.

Fig. 9 in Osteometric analysis of the scapula and humerus of Rangifer tarandus and Cervus elaphus: A contribution to the discrimination of Late Pleistocene cervids

Fig. 9. Scatterplot of the greatest breadth of the trochlea (BT) vs. the depth of the distal epiphysis (Dd) of the humerus of Rangifer tarandus and Cervus elaphus from Kiputz IX and other European sites.