Ministry of Agriculture & Rural Development
Collaboration for Agriculture & Rural Development
002/04VIE Project
Better Breeds of Common Carp (Cyprinus carpio L.)
for Small-scale Fish Farmers
Milestone 4: On-farm Trials and Uptake of Improved Breeds of
Common Carp
Christopher M Austin
1
, Tuan Anh Pham
2
, Binh Thanh Thai
2
, Hung Quang Le
2
1
School of Science and Primary Industries, Charles Darwin University, Darwin Northern
Territory 0909, Australia
2
Research Institute for Aquaculture No 1, Dinh Bang, Tu Son, Bac Ninh, Vietnam
Appendices 33
Reference 34
3
List of Figures
Fig 2.1. Rice field used for farm trials in Yen Bai province 9
Fig 2.2. Farmer’s pond in Thai Nguyen province 9
Fig 2.3. Measuring common carp 11
Fig 2.4. Ethnic people harvesting common cap in rice field in Yen Bai province 12
Fig 2.5. Harvesting common carp in pond in Thai Nguyen 13
Fig 2.6. A farmer is happy with common carp growth 13
Fig 3.1. Daily growth rate of HP3 and LOC common carp strains in each of 18 farms 15
Fig 3.2. Example of relative growth of three strains of common carp in rice field in Yen
Bai province after six months of culture 18
Fig 3.3. Daily growth rate of HP3, H3B and LOC common carp strain in each of 11 farms
in Yen Bai and Thai Nguyen provinces 18
Fig 3.4. Daily growth rate of HP3, VNW and LOC common carp strain for a period of 10
months in each farm in Yen Bai and Thai Nguyen provinces 20
Fig 3.5. Daily growth rate of HP3, H3B, VNW and LOC common carp strains in 3 farms.
22
Fig 3.6. Common carp from HP3 strain after seven months of cultured in a high input feed
farm in Thai Nguyen province 23
Fig 3.7. Proportion of genetically improved common carp fry and fingerlings cultured in
Vinh Phuc, Thai Nguyen and Yen Bai provinces during 2004-2006 29
period of 10 months in 11 farms in Yen Bai and Thai Nguyen provinces.
Superscripts indicate significant differences among groups based on Tukey’s test.
17
Table 3.8. ANOVA table testing for differences in survival rate in relation to the effects of
common carp strains (HP3, H3B and LOC) 19
Table 3.9. ANOVA table testing for differences in daily growth rate in relation to the
effects of common carp strain (HP3, VNW and LOC) 19
Table 3.10. Daily growth rate of HP3, VNW and LOC common carp strains grown for a
period of 10 months in 5 farms in Yen Bai and Thai Nguyen provinces.
5
Superscripts indicate significant differences among groups based on Tukey’s test.
20
Table 3.11. ANOVA table testing for differences in survival rate in relation to the effects
of common carp strains (HP3, VNW and LOC) 21
Table 3.12. ANOVA table testing for differences in daily growth rate in relation to the
effects of common carp strain (HP3, H3B, VNW and LOC) 21
Table 3.13. Daily growth rate of HP3, H3B, VNW and LOC common carp strains for
period of 10 months in 3 farms in Yen Bai and Thai Nguyen provinces.
Superscripts indicate significant differences among groups based on Tukey’s test.
22
Table 3.14. ANOVA table testing for differences in survival rate in relation to the effects
of common carp strains (HP3, H3B, VNW and LOC) and culture types (low and
high feed input) 23
Table 3.15. Biomass of common carp strains in 11 farms with 3 strains (HP3, H3B and
LOC) and cultured for 300 days in Yen Bai and Thai Nguyen provinces 24
Table 3.16. ANOVA analyses of biomass of HP3, H3B, and LOC common carp strains.25
Table 3.17. ANOVA analysis of biomass of HP3 and LOC common carp strains 25
Table 3.18. Biomass of common carp strains in 18 farms with 2 strains (HP3 and LOC)
cultured for 300 days. Superscripts indicate significant differences among groups
The level of culture intensity for common carp varies from small scale extensive farming,
with fish deriving all their nutrition from natural pond productivity, through semi-
intensive farming using fertilization from organic material such as bran, agriculture by-
products and household wastes to high intensive culture system with high stocking
densities and the use of manufactured fish foods. Semi-intensive culture systems are the
most popular in Vietnam using ponds or a combination of ponds and rice field cultivation
(Austin et al., 2007a).
There are many factors that affect production and yield of farmed fish species, including
seed (fry and fingerlings) quality, feed type and rate, fertilisation and pond management,
including water exchange. Of these, seed quality, which is directly related to the genetic
quality of the broodstock used to produce the fry and fingerlings, has been identified as
being of major concern to researchers (Thai et al., 2006; 2007), but which is not generally
understood by farmers to be a potential issue affecting farm productivity (Austin et al.,
2007a).
7
In Vietnam there are many different local varieties of common carp that have been used
by farmers but they usually have small size and low growth rate (Tran, 1983). Over recent
times the Research Institute for Aquaculture No.1 (RIA-I) has bred genetically improved
common carp strains to enhance the productivity of small scale fish farms that utilise this
species. This program has used crossbreeding and mass and family selection
methodologies to produce genetically improved strains and is considered to have achieved
an average increase of 5% in growth rate per generation over a number of generations
(Thien and Thang, 1992). However, all the selective breeding and associated growth trials
have been conducted in research ponds, often without the availability of unselected lines
as control populations for comparative studies.
As a consequence, on-farm growth trials of different strains were undertaken to allow for a
Bai provinces. Representatives of these households were interviewed for the socio-
economic survey and participated in one of the farmer workshops on fish breeding and
selection held as part of this project.
As described in more detail below the experimental design could not be achieved due to
differential reproduction and survival of fry. Thus different farms were stocked with
different numbers of strains and in varying combinations. Further, fish could not be
harvested from several farms due to flooding and other management problems. Appendix
1 lists the farms that participated in the project, and details of their culture systems and
fish that were stocked and if data collection at harvest was possible.
2.2. Selection of common carp strains
Fours common carp strains were used for growth trials and included one strain (HP3)
recently produced through hybridization between the three blood Hungarian strain and a
recently imported pure line of Hungarian carp, the three blood Hungarian strain (H3B), an
unselected Vietnamese strain (VNW) and a locally available strain (LOC) produced from
broodstock available from the Yen Bai provincial hatchery. Genetic analysis of this strain
(Thai et al., 2006: 2007) indicates it represented a mixture of Indonesian, Hungarian and
Vietnamese strains with the latter strain predominating.
9.
Fig 2.1. Rice field used for farm trials in Yen Bai province
Fig 2.2. Farmer’s pond in Thai Nguyen province
2.3. Common carp rearing and experimental procedures
Common carp breeding was undertaken at the National Broodstock Centre Hai Duong.
Thuan Yen Bai Pond 1000 LF 100 100 100 300
Tap Thai Nguye
n
Pond 800 HF 120 120 240
Tuan Thai Nguye
n
Pond 1000 LF 100 100 100 300
Chung Yen Bai Pond 1000 HF 100 100 100 300
Lien Yen Bai Ricefield 1500 LF 113 113 113 113 450
Hom Yen Bai Ricefield 800 LF 80 80 80 240
Tho Yen Bai Pond 450 HF 75 75 150
Dieu Thai Nguye
n
Pond 600 LF 100 100 200
Ha Thai Nguye
n
Pond 1500 LF 113 113 113 113 450
Lieu Thai Nguye
n
Pond 1000 LF 145 55 100 300
Canh Thai Nguye
n
Pond 400 HF 60 60 120
Luat Thai Nguye
n
Pond 1000 LE 100 100 100 300
Nhan Yen Bai Pond 1500 LE 113 113 113 113 450
Truong Thai Nguye
n
Pond 500 HF 75 75 150
rice fields were fed by available foods from farmers’ households such as rice bran, corn
and cassava. A log book was provided to each farmer to keep a record of food inputs into
their experimental pond and other relevant information and this information was used to
classified ponds into high and low feed input. The farmers were visited on a monthly basis
by project staff to assist in record keeping (Fig 2.3). Fig 2.3. Measuring common carp.
2.4. Data collection and analysis
Inequalities in fry weight among strains after the three month nursing period was tested by
weighing a sample of 30 individuals to the nearest 0.1 g and analysed using a one –way
ANOVA. Prior to this analysis the FMax test was used to determine if variances amongst
strains were homogenous. 12
Pond trials were conducted for 300 – 330 days. Fish were harvesting by draining and by
netting. Data from were collected as fish wet weight to the nearest 0.1 g and length (snout
– caudal) measured to the nearest mm (Fig 2.4, 2.5 & 2.6). Fish were allocated to strain
based on the identification of the position of the CWT using a detector scanner (North
West Marine technology, Shaw Island, WA, American). To compare growth between
strains, fish weights were converted to daily growth rate (DGR) after first subtracting the
mean fingerling weight for that strain.
The appropriate statistical procedure for the experimental design for analyzing for
differences in growth rate is a three-way ANOVA with nesting. The first level of the
analysis allows partitioning of variance due to Feed Input as either low (LF) or high (HF),
the second level is Farmer, which is nested within level 1 and the third level is Fish Strain.
Due to the unequal numbers fry available for each of the four carp strains and their
stocking in different combinations into farms and the unavailability of data from a number
All analyses were conducted using the Excel and SPSS software packages.
3. Results
3.1. Fingerling growth rate
The average weight of common carp fingerlings after 60 days of nursing was 3.18 g. The
average weight of each common carp strain is given in Table 3.1. However, the difference
in body weigh among strains was not significantly different (P>0.05).
Table 3.1 Mean (± SD) of body length and weight of fingerling carp after 60 days of nursing
Carp strain Length (cm) Weight (g)
HP3 4.72 ± 0.70 3.38 ± 1.50
H3B 4.57 ± 0.56 2.82 ± 1.66
VNW 5.36 ± 1.28 4.21 ± 2.84
LOC 4.27 ± 0.74 2.29 ± 1.32
Total 4.73 ± 0.82 3.18 ± 1.83
3.2. Growth and survival of HP3 and LOC strains and effects of feed input
Growth rate for the HP3 and LOC strains were compared in 18 farms which included both
low and high feed input systems. Significant differences were observed for all factors and
for the interaction between production systems and strain (Table 3.2) (P<0.01). The mean
daily growth rate of HP3 strain (0.48g) was 60% higher than that of local strain (LOC)
(0.30g) (Table 3.3). Daily growth rate of each fish farm is present in Fig 3.1.
15
Table 3.2. ANOVA table testing for differences in daily growth rate in relation to the effects of
Fig 3.1. Daily growth rate of HP3 and LOC common carp strains in each of 18 farms.
This last finding is particularly significant as it indicates that while there is a significant
difference among strains, this difference is greatly diminished in production systems with
low feed inputs. Table 3.3 gives the average daily growth rate for the 2 strains in each
0.00
0.50
1.00
1.50
2.00
2.50
3.00
Luat Ha Ke Vinh Tuan Lieu Dieu Que Lich Lien Hom Nhan Thong Thuan Truong Hoan Tap Chung
Farm
DRG (g)
HP3
LOC
Low feeding rate High feeding rate
16
Low 28
21.29
a
0.86 11.72 29.33
High 8
32.44
b
6.31 14.17 62.00
Total 36
26.90
a
3.58 12.95 45.67
17
3.3. Growth rate and survival of HP3, H3B and LOC strains
Growth data from three strains, HP3, H3B and LOC were compared in 11 farms which
included 10 low and 1 high feed input systems. Significant differences were observed for
strain and farmer as presented Table 3.6. Table 3.7 gives the average growth rate for the 3
strains. The effect of the level of feed input could not be tested statistically due lack of
replicates. The differences between strains can be seen from Figure 3.2 and Table 3.7. The
daily growth rate of common carp in each farm is presented in Fig 3.3. Each strain was
significantly different on the basis of Tukey’s test with HP3>H3B>LOC.
Table 3.6. ANOVA table testing for differences in daily growth rate in relation to the effects of
18 Fig 3.2. Example of relative growth of three strains of common carp in rice field in Yen Bai
province after six months of culture. 0.000
0.200
0.400
0.600
0.800
1.000
1.200
Total 23859.09 33
Corrected Total 4267.46 32
3.4. Growth rate and survival for HP3, VNW and LOC Strains
Growth data from three strains, HP3, VNW and LOC were compared in 5 farms which
included 4 low and 1 high feed input systems. Significant differences were observed for
both strain and farmer factors as presented Table 3.9. Table 3.10 gives the average growth
rate for the 3 strains. While the effect of production system could not be tested statistically
due to lack of replicates for this effect and the differences between strains and farms can
be seen from Figure 3.4. Each strain was significantly different on the basis of Tukey’s
test with HP3>VNW>LOC.
Table 3.9. ANOVA table testing for differences in daily growth rate in relation to the effects of
common carp strain (HP3, VNW and LOC).
.
Source Type III Sum of Squares df Mean Square F Sig.
Corrected Model 4.12 6 0.69 55.05 0.00
Intercept 17.22 1 17.22 1381.20 0.00
Farm 3.13 4 0.78 62.84 0.00
Strain 1.08 2 0.54 43.40 0.00
Error 3.74 300 0.01
Total 25.74 307
Corrected Total 7.86 306
20
Table 3.10. Daily growth rate of HP3, VNW and LOC common carp strains grown for a period
DRG (g)
HP3
VNW
LOC
Fig 3.4. Daily growth rate of HP3, VNW and LOC common carp strain for a period of 10 months
in each farm in Yen Bai and Thai Nguyen provinces.
The results of the survival rate of three common carp strains (HP3, VNW and LOC)
showed no significant differences between farms (Table 3.11). Although survival rate of
HP3 was the highest (20.57%) there had no significant difference comparing with other
two strains (VNW = 17.98% and LOC = 18.49%). 21
Table 3.11. ANOVA table testing for differences in survival rate in relation to the effects of
common carp strains (HP3, VNW and LOC).
Source Type III Sum of Squares df Mean Square F Sig.
Corrected Model 87.19 6 14.53 2.28 0.14
Intercept 5417.29 1 5417.29 850.77 0.00
Farm 68.18 4 17.04 2.68 0.11
Strain 19.01 2 9.51 1.49 0.28
Error 50.94 8 6.37
Total 5555.42 15
months in 3 farms in Yen Bai and Thai Nguyen provinces. Superscripts indicate significant
differences among groups based on Tukey’s test.
Strain N Mean Std Min Max
HP3 71
0.26
a
0.08 0.10 0.46
H3B 62
0.17
b
0.09 0.04 0.38
VNW 58
0.17
b
0.07 0.03 0.38
LOC 57
0.13
c
0.06 0.02 0.24
Total 248
0.18
C
0.08 0.05 0.370.00
0.05
0.10
0.15
Table 3.14. ANOVA table testing for differences in survival rate in relation to the effects of
common carp strains (HP3, H3B, VNW and LOC) and culture types (low and high feed input).
Source Type III Sum of Squares df Mean Square F Sig.
Corrected Model 90.87 5 18.17 4.33 0.05
Intercept 4161.47 1 4161.47 991.99 0.00
Farm 57.19 2 28.60 6.82 0.03
Strain 33.68 3 11.23 2.68 0.14
Error 25.17 6 4.20
Total 4277.52 12
Corrected Total 116.04 11
Fig 3.6. Common carp from HP3 strain after seven months of cultured in a high input feed farm
in Thai Nguyen province.
3.6. Common carp biomass production in farms stocked with three common carp
strain (HP3, H3B, LOC)
Common carp production was compared for 3 strains in 11 farms. Biomass of common
carp from 11 farms is presented in Table 3.23. Significant differences were observed
between farms and strains of common carp (Table 3.24). The pair-wise comparison
indicated difference in biomass of common carp between farms and between strains using
Tukey’s test. Biomass of three common carp strains ranged from 3.16g/m
2
(LOC) to
4.80g/m
2
(HP3).
H3B 100 2.82 14 22.45 14.00 0.07 0.03 0.47
LOC 100 2.29 17 16.10 17.00 0.05 0.05 0.41
Que 1000 LF HP3 100 3.38 36 59.35 36.00 0.20 1.80 3.20
H3B 50 2.80 11 56.74 21.00 0.19 0.46 1.79
LOC 150 2.29 33 53.68 22.00 0.18 1.43 1.77
Vinh 800 LF HP3 80 3.38 20 62.73 25.00 0.21 1.23 2.35
H3B 80 2.82 15 53.78 18.89 0.18 0.73 1.52
LOC 80 2.29 22 46.51 27.50 0.16 1.05 1.92
Thong 1000 LF HP3 100 3.38 22 49.00 22.00 0.16 0.74 1.62
H3B 100 2.82 21 44.00 21.00 0.15 0.64 1.39
LOC 100 2.29 22 35.67 22.00 0.12 0.56 1.18
Lien 1500 LF HP3 113 3.38 25 83.96 22.12 0.28 1.14 2.79
H3B 113 2.82 20 58.72 17.70 0.20 0.57 1.56
LOC 113 2.29 30 41.66 26.55 0.14 0.66 1.66
Ha 1500 LF HP3 113 3.38 20 102.67 17.70 0.34 1.11 2.73
H3B 113 2.82 21 79.93 18.58 0.27 0.91 2.23
LOC 113 2.29 22 54.24 19.47 0.18 0.62 1.58
Nhan 1500 LF HP3 113 3.38 21 59.88 18.58 0.20 0.58 1.67
H3B 113 2.82 16 20.61 14.16 0.07 0.01 0.44
LOC 113 2.29 19 15.66 16.81 0.05 0.03 0.40
Stocking Harvesting 25
Total 2198.60 36
Corrected Total 1449.39 35