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81 results for “Clarias gariepinus”
Fig. 2 in Microsatellite Variability Of Two Populations Of Clarias Gariepinus (Siluriformes, Clariidae) In Nigeria
Fig. 2. Genetic dendrogram of C. gariepinus from two vegetation zone (Lokoja and Asejire) of Nigeria.
Fig. 3 in Heterogeneity Studies Of Wild Clarias Gariepinus (Osteichthyes, Clariidae) Using Sds-Polyacrylamide Gel Electrophoresis
Fig. 3. Dendrogram obtained from Classical Cluster analysis using Paired group Bray-Curtis similarity index on C. gariepinus from two natural populations in Ado-Ekiti and Ilesa.
Fig. 2 in Heterogeneity Studies Of Wild Clarias Gariepinus (Osteichthyes, Clariidae) Using Sds-Polyacrylamide Gel Electrophoresis
Fig. 2. Dendrogram from Classical Cluster analysis using Paired group Bray-Curtis similarity index on Clarias gariepinus obtained in Ilesa, Osun State.
Fig. 1 in Heterogeneity Studies Of Wild Clarias Gariepinus (Osteichthyes, Clariidae) Using Sds-Polyacrylamide Gel Electrophoresis
Fig. 1. Dendrogram obtained from Classical Cluster analysis using Paired group Bray-Curtis similarity index on Clarias gariepinus in Ado-Ekiti.
Fig. 2 and table 3 in Phenotypic Diversities Of Four Populations Of Clarias Gariepinus (Siluriformes, Clariidae) Obtained From Ogun And Ondo State Waterbodies In South-Western Nigeria
Fig. 2 and table 3 illustrate the values of PCA loadings for the morphometrics of Clarias gariepinus obtained from the four Rivers showing Pre-ventral distance (PVD) as the trait with the highest variation.
Plate 1 in Incidence of parasitic infection in adult and juvenile Clarias gariepinus in a private fish farm, Yola, Adamawa state
Plate 1: Adult Clarias gariepinus placed on adissecting board after measurement and weighing for dissection
Fig 2 in Growth performance, nutrient utilization and survival rate of Clarias gariepinus fed varied inclusion of processed Moringa oleifera diets
Fig 2: Biweekly growth performance of Clarias gariepinus fed 3% and 5% inclusion of Moringa Processed diets
Fig. 2 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 2. Scanning electron micrographs of Glossidium pedatum. (A) Round oral sucker, (B) spine surrounding the oral sucker (C) location of the genital pore and a protruding cirrus, (D) structure of the cirrus sac (abbreviations: pl-papillae like lappet; os-oral sucker; pp-papillae; dp-dome papillae; vs-ventral sucker; gp-genital pore; c -cirrus; rp-rows of small papillae).
Fig. 5 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 5. Phylogenetic relationships of Tylodelphys mashonensis (Sudarikov, 1971) to other Diplostomidae based on cox1. Phylogram was reconstructed using Bayesian Inference (BI) with Diplostomum spathaceum (Rudolphi, 1819) as an outgroup. Nodal values <0.90 (BI) are indicated by dashes (sequences of the present study are highlighted in bold).
Fig. 3 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 3. Phylogenetic relationships of Glossidium pedatum Loos, 1899 to other members of Plagiorchioidea based on 28S rDNA. Phylogram was reconstructed using Bayesian Inference (BI) with Alloglossidium corti (Lamont, 1921) as an outgroup. Nodal values <0.90 (BI) are indicated by dashes (sequences of the present study are highlighted in bold).
Fig. 1 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 1. Geographical location of the study area: A– Kenya shaded on the African continent; B – shows position of Nyandarua County in Kenya; C – indicates the position of the Lake Ol'Bolossat and the sampling sites (S1–S3).
Fig. 4 in Tegumental topography and molecular characterisation of two trematodes (Platyhelminthes: Digenea) from Clarias gariepinus (Burchell, 1822) in Kenya
Fig. 4. Scanning electron micrographs of Tylodelphys mashonensis. (A) ventral surface ultrastructure, (B) sensory papillae surrounding the oral sucker (C) ventral sucker surrounded by small and large papillae, (D) well organized holdfast organ with spines (abbreviations: ps-pseudo suckers, os-oral sucker, ho- holdfast organ, vs-ventral sucker, pp-papillae, sp-symmetrical papillae, lp- large papillae, hf-holdfast fissure).
Figure 2 in Standard weight equations of two sub-/tropic nonnative freshwater fish, Clarias gariepinus and Oreochromis niloticus, in the Sakarya River Basin (NW Turkey)
Figure 2. Distribution of the residuals used to investigate potential length-bias in the standard weight (W ) equation for C. gariepinus (a) and O. niloticus (b) from the s Sakarya River Basin (residuals = standardized residuals of the regression; fitted values = values obtained by the model fit).
Figure 1 in Standard weight equations of two sub-/tropic nonnative freshwater fish, Clarias gariepinus and Oreochromis niloticus, in the Sakarya River Basin (NW Turkey)
Figure 1. Area of collection of the data (black rectangle = Sakarya River Basin; yellow dots = locations of the field stations within the Sakarya River Basin) (courtesy of Google Earth).
Fig. 2 in Oxidative stress biomarkers in the African sharptooth catfish, Clarias gariepinus, associated with infections by adult digeneans and water quality
Fig. 2. Monthly variation of physico-chemical parameters during the fish collection period, October 2016–September 2017. A– pH; B– Electrical conductivity; C– Temperature; D– Dissolved oxygen; E– Salinity; F– Turbidity; G– Total dissolved solids.
Fig. 1 in Oxidative stress biomarkers in the African sharptooth catfish, Clarias gariepinus, associated with infections by adult digeneans and water quality
Fig. 1. Various maps of the Incomati River showing the position of the sampling site. A– Mozambique shaded on the African continent; B– shows position of Maputo Province in Mozambique; C– indicates the position of the Incomati River and the sampling site.
Fig. 5 in Oxidative stress biomarkers in the African sharptooth catfish, Clarias gariepinus, associated with infections by adult digeneans and water quality
Fig. 5. Principal Component Analysis (PCA) of physico-chemical variables, biomarkers and parasitism in Clarias gariepinus collected in the Incomati River in Mozambique. Two principal components (PC1 and PC2) explained 45.45% of the total variation between water variables, biomarkers and occurrence of parasites. The EC, TDS and salinity (SAL) are associated with Component 1 while LPX, CAT, SOD, turbidity (TB) and temperature (T) are negatively associated with these variables. CI = co-infection; IM = M. nkomatiensis intensity; IG = G. pedatum intensity, UN = uninfected.
Fig. 10 in Camallanid nematodes from Clarias gariepinus (Burchell, 1822) in the Crocodile River, Gauteng, South Africa: Exploring diversity and divergence in an acid-mine drainage impacted environment
Fig. 10. Bar graphs showing the ratio of life stages and sexes in each sample. A- Procamallanus (Procamallanus) pseudolaeviconchus Moravec and van As, 2015. B- Paracamallanus cyathopharynx (Baylis, 1923). Prevalence of each group in each month is given in the line graphs. F = female, M = male, L = larvae, US = unknown sex.
Fig. 8 in Camallanid nematodes from Clarias gariepinus (Burchell, 1822) in the Crocodile River, Gauteng, South Africa: Exploring diversity and divergence in an acid-mine drainage impacted environment
Fig. 8. Lateral view of isolated buccal capsules of Paracamallanus specimens, morphotypes A and B. (i). Brightfield. (ii). Epifluorescence [Filter-set 09 (Ex. 470/40)]. (iii). SEM. 1 = anterior part of posterior capsule; 2 = posterior part of posterior capsule; t = trident; ellipse = elliptical shape of capsule; rectangle = rectangular shape of capsule.
Fig. 9 in Camallanid nematodes from Clarias gariepinus (Burchell, 1822) in the Crocodile River, Gauteng, South Africa: Exploring diversity and divergence in an acid-mine drainage impacted environment
Fig. 9. Principal Component Analyses (PCA) of Paracamallanus morphometry collected from Clarias gariepinus (Burchell, 1822). A- PCA using morphometric ratios for both males and females. B- PCA using buccal capsule ratios for both males and females. Each parasite is indicated as a dot, with the fill, shape and colour corresponding to morphotype and lineage (refer to key). F = female; M = male.
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International Brain Laboratory public data
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OpenNeuro
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