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10 results for “spillback”
Fig. 1 in Spillover and spillback risks of ectoparasites by an invasive squirrel Callosciurus erythraeus in Kanto region of Japan
Fig. 1. Location map of the study areas. The Pallas's squirrels examined in this study were collected by extermination programs operated by the local governments of Yokohama and Yokosuka. Detailed information on the sampling localities is refrained due to the intension of the cooperative organizations.
Fig. 3. NMDS plot for the parasite infracommunity composition recovered from 52 in Spillover and spillback risks of ectoparasites by an invasive squirrel Callosciurus erythraeus in Kanto region of Japan
Fig. 3. NMDS plot for the parasite infracommunity composition recovered from 52 host individuals. The influence of each parasite's abundance by discriminating the developmental stage on the score components of the two axes is represented by broken lines. The relationships with environmental variables are indicated by gray arrows. Abbreviations are as follows: M: male, F: female, YH: Yokohama, YS: Yokosuka, HfN: nymph of Haemaphysalis flava, HfL: larva of H. flava, Lep: larva of Leptotrombidium spp., EkA: adult of Enderleinellus kumadai, EkL: larva of E. kumadai, NoA: adult of Neohaematopinus callosciuri, NoL: larva of N. callosciuri, Ca: Ceratophyllus anisus, Ci: Ceratophyllus indages indages.
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.)
Fig. 2 in Spillover and spillback risks of ectoparasites by an invasive squirrel Callosciurus erythraeus in Kanto region of Japan
Fig. 2. Infracommunity richness by discriminating the study area and host sex.
ScienceDex guides
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