Fisheries and Aquaculture Journal

Fisheries and Aquaculture Journal
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Research Article - (2018) Volume 9, Issue 2

Studies on the Biology of Synodontis victoriae in the Nyanza Gulf of Lake Victoria, Kenya

Edwine Yongo* and Alex Wairimu
Department of Fisheries and Aquatic Sciences, University of Eldoret, P.O. Box 1125-30100 Eldoret, Kenya
*Corresponding Author: Edwine Yongo, Department of Fisheries and Aquatic Sciences, University of Eldoret, P.O. Box 1125-30100 Eldoret, Kenya, Tel: +254 717 211 64 Email:

Abstract

Fish samples (401) were collected weekly between May to July 2015 from commercial catches in the Nyanza Gulf of Lake Victoria, Kenya. The Fork length (cm FL), weight (g) and sex were determined. A total of 288 (71.8%) were female while 107 (26.7%) were males, sex ratio; 1.0:2.7 (male: female). Size of females ranged from 9.0 cm to 17.6 cm FL, mean (± SD) 13.6 cm ± 1.3 cm FL and weighed between 13.0 g and 99.0 g, mean 47.5 g ± 13.9 g. Length of males ranged from 7.0 cm to 15.6 cm FL, mean 12.8 cm ± 1.3 cm FL and weighed between 7.0 and 62.0 g, mean 36.2 g ± 9.9 g. Sex dimorphism was observed as female fish were significantly larger than males (p<0.05). The length frequency showed a unimodal distribution with modal class at 13 cm FL. Male, female and both sexes showed negative allometric growth pattern (b<3). The fish had a good condition with values equal to 1. The smallest mature male and female fish were 11.2 cm and 11.3 cm FL, respectively. The length at 50% maturity was estimated at 13.0 cm FL for male and 12.0 cm FL for female fish. The study has thus provided baseline information on some aspects of the biology of Synodontis victoriae that are limited in the lake.

Keywords: Synodontis Victoriae; Maturity; Condition; Length- Weight

Introduction

Synodontis victoriae is a species in the order Siluriformes (Catfish) of Mochokidae family. They are also known as squeakers due to their ability to make stridulatory sounds through their pectoral fin spines when handled or disturbed [1]. They have 1 dorsal spine, 6-7 dorsal soft rays, 16-21 mandibular teeth, maxillary barbels, dark spots and spotted caudal fin. The fish is common in Africa, occurring mostly in Lakes Kyoga and Victoria, Victoria Nile, lower Kagera River and Malagarasi drainage [2]. S. victoriae inhabits lakes at depths of more than 20 m over soft bottoms although they also occur over hard substrates in waters above 13 m deep. They are found in creeks, ponds, streams, lakes and rivers [1]. The fish can tolerate low levels of dissolved oxygen [3]. They mature at about 8 cm to 10 cm FL and grow to attain a maximum length of 35 cm FL [4]. S. victoriae are oviparous reproducing with the flooding period of the rainy season and are found at temperatures of between 23°C to 27°C [5]. They are omnivorous feeding on a wide spectrum of different foods [1]. Wanyanga et al. [6] reported that the diet of S. victoriae primarily comprise of molluscs, crustaceans, insects, detritus and fish scales.

S. victoriae are prized ornamental because of their striking pigmentation body patterns and display unusual behaviors such as upside down swimming. Furthermore like any other fish they play an important role by providing food for human consumption and employment opportunities. They are potamodromous and their decline in Lake Victoria has been attributed to intensive fishing using small mesh gillnets and traps at the river mouths where ripe females and males congregate on their way to spawn in the riverine environment. Apart from over fishing, most of these species are threatened by modification of riverine regimes by human activities such as farming, settlement, urban and industrial effluents and the introduction of alien species. This study determined some aspects of the biology of S. victoriae in Lake Victoria.

Materials and Methods

This study was conducted in the Nyanza Gulf of Lake Victoria, Kenya (56°17ˈ43.008˝N 30°58ˈ57.32˝E; 0°08ˈ40.7˝S, 34°44ˈ12.4˝E). The fishery of S. victoriae within the gulf is mainly by gillnetting (2.0 inches to 4.0 inches mesh-size). Samples (401) of S. victoriae were collected weekly from commercial catches between May to July 2015. The fish were measured Fork length (cm FL) and weighed (0.1 g) using an electronic balance. Sex for the fish was determined using the keys of Lagler (Table 1) [7]. Length at 50% maturity was estimated by fitting frequency data of mature individuals by lengths to a logistic curve.

Maturity stage Male Female
Stage I: Immature Testes colourless Eggs invisible to naked eye
Stage II: Developing Testes translucent Small eggs seen using magnifying glass
Stage III: Mature Anterior testis whitish with short finger-like processes Eggs clearly discernible to eye; ovaries orange-reddish
Stage IV: Ripe Testes large and produces milt drops under slight pressure; Ovaries fill ventral cavity; eggs light green, completely round and fall from ovary with little pressure
Stage VI: Spent Testes thread-like with no granules and are pink-white shrivelled bodies No opaque eggs left in ovaries; ovaries large but flabby

Table 1: Maturity stages of S. victoriae according to Lagler [7].

The length-weight relationship was estimated using the formula:

image

The relative condition factor was calculated as follows:

image

Results

The length of fish sampled ranged from 7.0 cm to 18.0 cm FL. The size frequency showed a unimodal distribution with modal class at 13 cm FL (Figure 1). Out of 401 fish, 288 (71.8%) were females while 107 (26.7%) were males, giving an overall sex ratio of 1.0:2.7 (male: female). Chi-square test showed that females were significantly more than males and deviated from the expected 1:1 ratio (χ2= 82.94, p<0.05). However, females were not more than males for the fish below 12 cm FL (Table 2, p>0.05). The size of female fish ranged from 9 cm to 17.6 cm FL, mean (± SD) 13.6 cm ± 1.3 cm FL and weighed between 13 g and 99.0 g, mean 47.5 g ± 13.9 g. The length of male fish ranged from 7.0 cm to 15.6 cm FL, mean 12.8 cm ± 1.3 cm FL and weighed between 7.0 g and 62 g, mean 36.2 g ± 9.9 g. Sex dimorphism was observed with female fish being significantly larger (F=31.58, p<0.05) and heavier (F=59.72, p<0.05) than males. Male, female and both sexes of S. victoriae showed negative allometric growth with values of regression slope b being 2.59, 2.97 and 2.91 (Figure 2, b<3). The 95% confidence intervals (CI) of the slopes were 2.33-2.84, 2.82-3.12, 2.78-3.04 for males, females and both sexes. Males, females and both sexes recorded mean (± SD) condition factor above 1 (Table 3). The smallest mature male and female fish were 11.2 cm and 11.3 cm FL, respectively. The length at 50% maturity was estimated at 13.0 cm FL for male and 12.0 cm FL for female fish (Figure 3).

fisheries-and-aquatic-Gulf-Lake-Victoria

Figure 1: Size frequency distribution of S. victoriae from the Nyanza Gulf of Lake Victoria.

Length (cm FL) Males (M) Females (F) χ2 p
<10 1 2 0.33 0.564
10-12 23 19 0.38 0.537
12-14 60 143 33.94 0
14-16 23 114 60.45 0
16-18 0 10 10 0.002
Total 107 288 82.94 0

Table 2: Ratio of male (M) to female (F) of S. victoriae from the Nyanza Gulf by length group.

Category n Mean ± SD Range
Males 107 1.006 ± 0.106 0.792-1.237
Females 288 1.007 ± 0.106 0.710-1.311
Both sexes 401 1.006 ± 0.117 0.693-1.329

Table 3: Relative condition factor of S. victoriae from the Nyanza Gulf of Lake Victoria.

fisheries-and-aquatic-Length-weight-relationship

Figure 2: Length-weight relationship of S. victoriae from Nyanza Gulf of Lake Victoria.

fisheries-and-aquatic-maturity-female-male

Figure 3: Length at 50% maturity of female and male S. victoriae from the Nyanza Gulf.

Discussion

This study showed that females of S. victoriae were significantly more than males with an overall ratio of 1.00:2.70 (Male: Female). This is in agreement with Oboh et al. [8] reporting a sex ratio of 1.00:1.35 (Male: Female) for Synodontis Schall from Jamieson River in Nigeria. Similarly, Adeyemi [9] reported a ratio of 1.00:1.53 (Male: Female) for Synodontis robbianus from River Niger in Nigeria. However, for S. schall from River Nile in Egypt, Imam et al. [10] reported no difference in the sex ratio 1.00:1.04 (Male: Female). Akombo et al [11] found a ratio of 1.00:1.08 (Male: Female) for S. schall from River Benue in Nigeria. Olele et al. [12] reported a sex ratio of 1.00:1.30 (Male: Female) for Synodontis nigrita from Onah Lake in Nigeria. The length at 50% maturity in males and females of S. victoriae were 13.0 cm and 12.0 cm FL, respectively. However, females and males of S. schall reached maturation at 28.2 cm and 29.4 cm, respectively [10]. The size at maturity of Synodontis eupterus from River Rima in Nigeria were 7.2 cm TL (Female) and 7.0 cm TL (Male) [13]. Knowledge on size at maturity guides to set mesh sizes that protects spawning fish and juveniles. The fish showed a slightly negative allometric growth pattern (b<3) with condition values equal to 1. Similar findings have been reported for Rastrineobola argentea and Lates niloticus in the same lake. The b value can be used as an indicator of food intake and may differ according to biotic and abiotic factors, food availability and habitat type. Changes in the zooplankton communities in Lake Victoria [14] may affect the food items for S. victoriae thus influencing its condition. The fish condition also depends on season, sex and life stages [15-18]. This study has provided baseline information on the biology of S. victoriae that are limited in the lake. However, there is still need for further research on other aspects.

References

  1. Friel JP, Vigliotta TR (2006) Synodontis acanthopera, a new species from the Ogooue River system, Gabon with comments on spiny ornamentation and sexual dimorphism in Mochokid Catfishes (Siluriformes: Mochokidae). Zootaxa 1125: 45-56.
  2. Koblmuller S, Sturmbauer C, Verheyen E, Meyer A, Salzburger W (2006) Mitochondrial phylogeny and phylogeography of East Africa squeaker (Siluriformes: Synodontis). BMC Evol Biol 6: 49-64.
  3. Yongo E, Outa N (2017) Spatial distribution and abundance of zooplankton communities in Lake Victoria, Kenya. Int J Fish Aqua Res 2: 33-35.
  4. Gosse JP (1986) Check-list of the freshwater fishes of Africa (CLOFFA). ISNB, Brussels, MRAC, Tervuren. Paris 2: 105-152.
  5. Philippe L, AntoineC, Pierre G, Pierre V, Claude JP, et al. (2006) Studies on the biology of two species of Catfish Synodontis schall and Synodontis nigrita (Ostariophysi: Mochokidae) from the Oueme River, Benin. Belg J Zool 136: 193-201.
  6. Wanyanga A, Yongo E, Mwangudza P (2016) Diet of Synodontis victoriae (Mochokidae) from Kunya beach Lake Victoria, Kenya. Int J Fish Aqua Res 1: 11-15.
  7. Lagler KF (1971) Capture, sampling and examination of fishes. In: Ricker W.E. (Ed), Methods for assessment of fish production in freshwaters (2nd Editor). International Biological Programme 3: 7-44.
  8. Oboh IP, Ogbeibu AE, Ogoanah SO (2013) Gonadal Development, Fecundity and Spawning Pattern of Synodontis Schall (Pisces: Mochokidae) From Jamieson River, Nigeria. Research and Reviews: Journal of Zoological Sciences 1: 13-23.
  9. Olusegun AS (2011) Length-weight, Length-length Relationship and Condition Factor of Synodontis robbianus at Idah Area of River Niger, Kogi State, Nigeria. Pakistan Journal of Nutrition 10: 505-508.
  10. Imam AA, Mekkawy A, Hassan A (2011) Some Reproductive Parameters of Synodontis schall (Bloch and Schneider, 1801) from the River Nile, Egypt. Journal of Fisheries and Aquatic Studies 6: 456: 471.
  11. Akombo PM, Akange ET, Adikwu IA, Araoye PA (2014) Length-weight relationship, condition factor and feeding habits of Synodontis schall (Bloch and Schneider, 1801) in river Benue at Makurdi, Nigeria. International Journal of Fisheries and Aquatic Studies 1: 42-48.
  12. Olele NF, Etim L (2011) Some aspects of the biology of Synodontis nigrita (Curvier and Valencienes, 1864) in Onah Lake, Asaba, Nigeria. ARPN. Journal of Agricultural and Biological Science 6: 56-63.
  13. Shinkafi BA, Daneji AI (2011) Morphology of the Gonads of Synodontis eupterus (Boulenger) from River Rima, North-western, Nigeria. International Journal of Zoological Research 7: 382-392.
  14. Yongo E, Outa N, Ngodhe SO (2017) Effects of Water hyacinth (Eichhornia crassipes Solm) Infestation on water quality, fish species diversity and abundance in the Nyanza Gulf of Lake Victoria, Kenya. Int J Fish Aqua Res 2: 8-10.
  15. Le Cren ED (1951) The length-weight relationship and seasonal cycle in gonad weight and condition in the perch (Perca avescens). Journal of Animal Ecology 20: 201-219.
  16. Arslan M, Yildirim A, Bektas S (2004) Length-weight relationship of brown trout, Salmo trutta (L.) inhabiting Kan Stream, Çoruh basin, north-eastern Turkey. Turkish Journal of Fisheries and aquatic Sciences 48: 45-48.
  17. Yongo E, Manyala JO, Njiru JM, Outa NO, Kito K, et al. (2016) Length-weight relationship, Condition factor, Sex ratio, Gonadal Somatic Index and Size at Maturity of Omena, Rastrineobola argentea (Pellegrin, 1904) in Lake Victoria, Kenya. International Journal of Advanced Research 4: 1740-1746.
  18. Yongo E, Outa N, Kito K, Matsushita Y (2017) Some aspects of the biology of Nile perch, Lates niloticus, in the open waters of Lake Victoria, Kenya. Lakes and Reservoirs: Research and Management 20: 1-6.
Citation: Yongo E, Wairimu A (2018) Studies on the Biology of Synodontis victoriae in the Nyanza Gulf of Lake Victoria, Kenya. Fish Aqua J 9: 244.

Copyright: © 2018 Yongo E, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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