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Fig. 5 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 5. The relationship between the prevalence of Eimeria spp. oocysts in European bison feces measured by the Willis and modified McMaster techniques (each point represents an individual parasite species).

Fig. 1 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 1. Probability of detection of Eimeria spp. oocysts with the modified McMaster technique based on the number of oocysts detected using the Willis technique.

Fig. 4 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 4. The relationship between the prevalence of various taxa eggs/oocysts in European bison feces measured by the Willis and modified McMaster techniques (each point represents an individual taxon/genus, blue points stand for oocysts and red point for eggs). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Aug 2022View details →

Fig. 1 in An assessment of ectoparasites across highland and lowland populations of Leadbeater's possum (Gymnobelideus leadbeateri): Implications for genetic rescue translocations

Fig. 1. Fleas detected on the Leadbeater's possum (Gymnobelideus leadbeateri); Stephanocircus domrowi (panel A), Choristopsylla tristis (panel B), Wurunjerria warnekei (panel C), Acanthopsylla rothschildii rothschildii (panel D).

Fig. 3 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 3. Probability of detection of Trichostrongylidae eggs with the modified McMaster technique based on the number of eggs detected using the Willis technique.

Fig. 2 in Veterinary monitoring of gastrointestinal parasites in European bison, Bison bonasus designated for translocation: Comparison of two coprological methods

Fig. 2. Probability of detection of Trichuris sp. eggs with the modified McMaster technique based on the number of eggs detected using the Willis technique.

Fig. 7 in Parasite diversity and community structure of translocated Clarias gariepinus (Burchell) in South Africa: Testing co-introduction, parasite spillback and enemy release hypotheses

Fig. 7. Non-metric Multi-dimensional Scaling (nMDS) scatter plot explaining the diversity and abundance of the parasite infracommunities of Clarias gariepinus (Burchell) from Gariep Dam (GD), Great Fish River (GFR) and Riviersonderend River (RSE) in South Africa. The ordination illustrates the similarity between parasite infracommunities, with a Pearson's correlation vector overlay showing parasitic taxa with a correlation>0.1. Similarity levels (15, 30) were selected based on the hierarchical cluster analyses (Resemblance = 50) of Bray Curtis coefficients.

Fig. 6 in Parasite diversity and community structure of translocated Clarias gariepinus (Burchell) in South Africa: Testing co-introduction, parasite spillback and enemy release hypotheses

Fig. 6. Parasite infracommunity composition of Clarias gariepinus (Burchell) from Gariep Dam (GD), Great Fish River (GFR) and Riviersonderend River (RSE). A – abundance (N); B – species richness (S); C – Brillouin's diversity index (DB); D – Shannon-Wiener diversity index (H′); E – Simpson diversity index (D) and F – Pielou's evenness index (J′). The mean and 95% confidence interval of each index is presented. Significant differences are considered as p <0.05 and denoted with an asterisk (*) in a table for each index.

Fig. 5 in Parasite diversity and community structure of translocated Clarias gariepinus (Burchell) in South Africa: Testing co-introduction, parasite spillback and enemy release hypotheses

Fig. 5. Photomicrographs of A – Paracamallanus sp. and Argulus japonicus Thiele, 1900, B – dorsal view and C – ventral view. Scale bars: 20 μm (A); 1000 μm (A, B).

Fig. 4 in Parasite diversity and community structure of translocated Clarias gariepinus (Burchell) in South Africa: Testing co-introduction, parasite spillback and enemy release hypotheses

Fig. 4. Photomicrographs of Orientocreadium batrachoides Tubangui, 1831 (A – D) from the intestine and Tylodelphys mashonensis Beverley-Burton, 1963 (E – H) from the cranial cavity of Clarias gariepinus (Burchell) during the present study. White arrows indicate structures of taxonomic relevance. Abbreviations: Gp – genital pore, OS – oral sucker, Ph – pharynx, Ps – pseudosuckers, Vs – ventral sucker. Scale bars: 50 μm (F–H); 100 μm (B–D, E); 500 μm (A).

Fig. 2 in Parasite diversity and community structure of translocated Clarias gariepinus (Burchell) in South Africa: Testing co-introduction, parasite spillback and enemy release hypotheses

Fig. 2. Map depicting the distribution of A. the Asian tapeworm, Schyzocotyle acheilognathi (Yamaguti, 1934) and B. the branchiuran fish lice, Argulus japonicus Thiele, 1900 from freshwater fishes in South Africa. Dark grey shading indicates provinces where freshwater fish parasitological research has been conducted more frequently.

Fig. 3 in Parasite diversity and community structure of translocated Clarias gariepinus (Burchell) in South Africa: Testing co-introduction, parasite spillback and enemy release hypotheses

Fig. 3. Photomicrographs of Monogenea found from the gills of Clarias gariepinus (Burchell) during the present study. A, B – Quadriacanthus aegypticus ElNaggar et Serag, 1985; C, D – Quadriacanthus allobychowskiella Paperna, 1979; E, F – Quadriacanthus clariadis Paperna, 1961; G, H – Quadriacanthus fornicatus Francov´a et ˇRehulkov´a, 2017; I – Quadriacanthus pravus Francov´a et ˇRehulkova´, 2017. Black arrows indicate structures of taxonomic relevance. Hamuli (A, C, E, G, I); male copulatory organ with accessory piece (B, D, F, H). Scale bars: 10 μm (B, D, F, H); 20 μm (I); 25 μm (A, C, E, G).

Fig. 1 in Parasite diversity and community structure of translocated Clarias gariepinus (Burchell) in South Africa: Testing co-introduction, parasite spillback and enemy release hypotheses

Fig. 1. Map indicating the localities where Clarias gariepinus (Burchell) were collected during the present study. The orange overlay indicates the translocated distribution of C. gariepinus in South Africa. Dark grey shading represents provinces where freshwater fish parasitological research has been conducted more frequently. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Aug 2024View details →

Fig. 1 in Applying a modified streamlined disease risk analysis framework to a platypus conservation translocation, with special consideration for the conservation of ecto- and endoparasites

Fig. 1. An outline of how parasite conservation can be considered in translocation planning, reproduced from Carlson et al. (2020).

opencc-by-4.0May 2024View details →

Molecular insights into substrate translocation in an elevator-type metal transporter

This dataset contains biased simulation trajectories for the paper entitled "Molecular insights into substrate translocation in an elevator-type metal transporter." The trajectories are named based on the information provided in the paper. The deposited trajectories contain only the protein and zinc metal ions; due to size constraints, we retained only these components and removed the rest. The entire systems and additional input files are available upon request to the authors. The dataset comprises four folders named as follows:  First_scenario, Second_scenario, Third_scenario, and Last_scenario. To extract the contents of the compressed file (.tar.gz), use the following command line: tar -xzvf zip_transporter.tar.gz Each folder contains topology files and their corresponding trajectory files. The term "Rep" in the file names denotes the simulation replicates. For instance, "rep1" indicates the first simulation replicate mentioned in the paper. All analyses were performed using cpptraj and VMD software. Custom codes for performing the analyses are available at https://gitlab.msu.edu/jafarima/zip-transporter.git.

dryad40/100

Data for Integrated Step Selection Analysis of translocated female greater sage-grouse in the 60 days post-release, North Dakota 2018-2020

The data include used and random available steps at 11-hour resolution generated for 26 female greater sage-grouse in the 60 days post-translocation to North Dakota, with associated environmental predictors and individual information. The code fits individual habitat selection models in an Integrated Step Selection Analysis framework. Data used to fit the models described in: Picardi, S., Ranc, N., Smith, B.J., Coates, P.S., Mathews, S.R., Dahlgren, D.K. Individual variation in temporal dynamics of post-release habitat selection. Frontiers in Conservation Science (in review) Code used to implement the analysis is available on GitHub: https://github.com/picardis/picardi-et-al_2021_sage-grouse_frontiers-in-conservation

opencc-zeroSep 2021View details →

opencc-by-4.0May 2017View details →

Fig. 2 in Sauvegarde d'une fourmilière de Formica pratensis Retzius, 1783 (Hymenoptera, Formicidae) par translocation

Fig. 2. Illustrations des étapes clés de la translocation de la fourmilière de Formica pratensis réalisée à Gimel en date du 23 mars 2016. (Photos Jérôme Pellet et Vincent Sonnay)

opencc-by-4.0May 2017View details →

Fig. 1. A in Sauvegarde d'une fourmilière de Formica pratensis Retzius, 1783 (Hymenoptera, Formicidae) par translocation

Fig. 1. A gauche, ouvrière de Formica pratensis photographiée sur le dôme de la fourmilière transplantée. (Photo Jérôme Pellet) A droite, carte de la distribution de cette espèce en Suisse (répartition lacunaire reflétant les zones où des inventaires ont été réalisés). (© CSCF)