Use of a natural aquatic fern, Azolla microphylla, as a main component in food for the omnivorous-phytoplanktonophagous tilapia, Oreochromis niloticus L.

2004 ◽  
Vol 20 (6) ◽  
pp. 517-520 ◽  
Author(s):  
E. D. Fiogbe ◽  
J.-C. Micha ◽  
C. Van Hove
Biogenesis ◽  
2021 ◽  
Vol 17 (1) ◽  
pp. 39
Author(s):  
Suwondo Suwondo ◽  
Darmadi Darmadi ◽  
Muhammad Amin

This study aims to determine the growth of tilapia (Oreochromis niloticus) with the use of Azolla microphylla feed and its potential to produce a module design on the material for growth and development of living things in class XII odd semester KD 3.10 and KD 4.10.This research was conducted from May to August 2020 at Danau Selais LPPM Riau University. This study used 2 stages, namely. Phase I research used quantitative descriptive to determine the growth of tilapia on Azolla microphyla feed with different feeding percentages. Fish were grouped into 3 treatments and 1 control. Fish are reared in different cages with different percentage of feeding. The research parameters included absolute length growth, absolute weight growth, nisbi  growth rate, and survival rate.Phase II research is a module teaching material design that uses 2 stages, namely, the Analyze and Design stages.The results of the experimental stage of research, feeding Azolla microphylla affected the growth of tilapia (Oreochromis niloticus). P3 treatment (giving 5% Azolla microphylla from fish biomass) is the best dose in increasing the growth of tilapia. Resulted in the absolute length growth of 4.24 cm, absolute weight 11.72 g, 4.68% relative growth, 4,68% specific growth rate and 99.4% survival rate. The P3 treatment resulted in a growth which was much lower than the P0 treatment (control).


2017 ◽  
Vol 64 (1) ◽  
pp. 31
Author(s):  
Arnauld S. M. Djissou ◽  
Akito Ochiai ◽  
Shunsuke Koshio ◽  
Emile D. Fiogbe

In order to eliminate use of fishmeal in aquafeeds, we evaluated the effect of total replacement of fish meal by a mixture of earthworm (Eisenia foetida) and aquatic fern Azolla filiculoides in the diets of Nile tilapia Oreochromis niloticus (Linnaeus, 1758). The experiment was conducted in O. niloticus fingerlings (initial mean weight = 5.6±0.2 g) for a period of 60 days. Five experimental diets isoproteic (30.4±0.6% protein) comprising control diet A0 and four test diets (A1 to A4) without fish meal were formulated. To satisfy essential amino acids requirements in test diets, the ratios 2:1; 1:1; 1:2; 1:5 between A. filiculoides and earthworm meals were used respectively in total replacement of fish meal. The diets were tested in triplicate. On termination of the experiment, the final mean weights in the test diets (10.79 to 11.94 g) were lower than 14.9 g obtained in group fed control diet (p<0.05). The best growth performance and feed utilisation were obtained in fish fed test diets A1 and A4 (SGR = 1.25 and 1.26% day-1; FCR = 2.37 and 2.31 respectively). Excess of lysine in test diets was found to affect the feed utilisation.


2018 ◽  
Vol 2 (01) ◽  
pp. 14-19
Author(s):  
SUMOHARJO SUMOHARJO ◽  
MOHAMMAD MA’RUF ◽  
IRWAN BUDIARTO

Sumoharjo, Ma’ruf M, Budiarto I. 2018.Biomass production of Azolla microphylla as biofilter in a recirculating aquaculture system. Asian J Agric 2: 14-19. This study utilized macrophyte (Azolla microphylla Kaulf.) as biofilter and perhaps that biomass produced in aquaculture system can be potential for alternative feed. This experiment such a first step of that vision and was aimed to determine the Azolla microphylla growth rate and its efficiency in removing ammonia from a simple recirculating aquaculture system. The experimental units were set up in three different water flow, i.e. 3 lpm, 5 lpm, and 7 lpm onto the three different geometrically baseboard of Tilapia (Oreochromis niloticus) growing tanks (prism, rectangular and limas).The result showed that water flow did not give significant effect(P < 0.10) on the growth rate of Azolla.The lower water flow (3 lpm) resulted in the highest amonia biofiltration efficiency which can remove ammonia up to 32.2±3.0% of the total NH3-N and NH4+-N (TAN).


1999 ◽  
Vol 37 (1) ◽  
pp. 33-38 ◽  
Author(s):  
M. Jayakumar ◽  
M. Eyini ◽  
P. Selvinthangadurai ◽  
K. Lingakumar ◽  
A. Premkumar ◽  
...  

Author(s):  
T. Guha ◽  
A. Q. Siddiqui ◽  
P. F. Prentis

Tilapia, Oreochromis niloticus, is an economically important fish in Saudi Arabia. Elucidation of reproductive biology of this species is necessary for successful breeding program. In this paper we describe fine structure of testicular sperm cells in O, niloticus.Testes from young adult fish were fixed in gluteraldehyde (2%) and osmium tetroxide (1%), both in cacodyl ate buffer. Specimens were processed in the conventional way for electron microscopy and thin sections of tissues (obtained by cutting the blocks with a diamond knife) were stained by ura- nyl acetate and lead citrate. These were examined in a Carl Zeiss electron microscope operated at 40 kV to 60 kV. Sperm cells were obtained from testes by squeezing them in cacodyl ate buffer. They were fixed in gluteraldehyde (2%) in the same buffer, air dried, gold coated and then examined in a Philips scanning electron microscope (SEM) operated at 25kV.The spermatozoon of O. niloticus is consisting of head, midpiece and tail (Fig. 1).


Author(s):  
T. Guha ◽  
A. Q. Siddiqui ◽  
P. F. Prentis

The Primary Spermatocytes represent a stage in spermatogenesis when the first meiotic cell division occurs. They are derived from Spermatogonium or Stem cell through mitotic division. At the zygotene phase of meiotic prophase the Synaptonemal complex appears in these cells in the space between the paired homologous chromosomes. Spermatogenesis and sperm structure in fish have been studied at the electron microscope level in a few species? However, no work has yet been reported on ultrastructure of tilapia, O. niloticus, spermatozoa and spermatogenetic process. In this short communication we are reporting the Ultrastructure of Primary Spermatocytes in tilapia, O. niloticus, and the fine structure of synaptonemal complexes seen in the spermatocyte nuclei.


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