2002
DOI: 10.1016/s0165-7836(00)00291-5
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The biology of Clarias ebriensis Pellegrin, 1920 (Osteichthyes: Clariidae) in an African rainforest river basin

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Cited by 18 publications
(12 citation statements)
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“…The low FI in the month of November coincides with the peak breeding period for C. liocephalus (Yatuha 2012, unpublished data). Decline in FI during the peak reproductive period has been reported in other fish species (Dadzie ; Ezenwaji, ; Preciado et al ., ). In this study, we observed that ripe gonads, especially in females, filled almost the entire body cavity.…”
Section: Discussionsupporting
confidence: 61%
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“…The low FI in the month of November coincides with the peak breeding period for C. liocephalus (Yatuha 2012, unpublished data). Decline in FI during the peak reproductive period has been reported in other fish species (Dadzie ; Ezenwaji, ; Preciado et al ., ). In this study, we observed that ripe gonads, especially in females, filled almost the entire body cavity.…”
Section: Discussionsupporting
confidence: 61%
“…Aquatic insects in general and dipteran larvae in particular were found to be the most frequent prey in the diet of C. liocephalus across all sites, showing C. liocephalus' preference for dipteran larvae. This preference has been reported in C. gariepinus (Yalcin, Akyurt & Solak, ) and C. ebriensis (Ezenwaji, ) and has been attributed to the high abundance of the prey in the habitat (Yalcin, Akyurt & Solak, ). Clarias liocephalus seem to forage on the available and dominant prey as a generalist, but prefers dipteran larvae when they are present in the habitat.…”
Section: Discussionsupporting
confidence: 56%
“…In Okpara Stream, males of H. fasciatus reached their size at first maturity at a total length (L 50 = 10.98 cm-TL) higher than that of females (L 50 = 9.22 cm -TL). This sexual difference in L 50 , mostly tardive in males was reported for several fish species such Chrysichthys nigrodigitatus and Chrysichthys auratus (Lalèyè et al, 1995), Clarias ebriensis (Ezenwaji, 2002), Labeo horie (Dadebo et al, 2003), Labeo victorianus (Rutaisire and Booth 2005); Heterotis niloticus (Adité et al, 2006), Clarias gariepinus, Clarias ebriensis, Schilbe intermedius, Schilbe mystus, Synodontis schall (Chikou et al, 2011), Sarotherodon galileus (Gbaguidi and Adite 2016) etc. Genetic factors including sexual dimorphism of growth and habitat conditions such as physicochemical variations and food resource availabilities could greatly affect the size at first sexual maturity (Wootton, 1998;Koné et al 2011;Tembeni et al 2014).…”
Section: Length At First Sexual Maturation (Tl50)supporting
confidence: 68%
“…This apart from intermittent deaths reduces fish tegument value and patho-physiology of visceral organs that provide micro-habitats for them in their fish hosts by the excysted metacercariae. Therefore, the chance to have most reproductive success than other species depends on availability of more excysted forms in each host (Echi et al, 2012).…”
Section: Introductionmentioning
confidence: 99%