Growth rate Width of M lyrata culture in Influent Pond, by Density Growth rate thickness of M.. Growth rate Thickness of M lyrata culture in Influent Pond, by Density Growth rate weigh
Trang 1Ministry of Agriculture & Rural Development
CARD Project Progress Report
027/05VIE: Development of clam culture for
improvement and diversification of
livelihoods of the poor coastal communities
in Central Vietnam
MS2: First Six-Monthly Report
Trang 21 Institute Information
Project Name Development of clam culture for improvement
and diversification of livelihoods of the poor coastal communities in Central Vietnam (Project No: 027/05VIE)
Vietnamese Institution Aquaculture Research Sub-Institution of North
Central Vietnam (ARSINC)
Vietnamese Project Team Leaders Mr Nhu Van Can (Project Director)
Mr Chu Chi Thiet (Project Manager)
Australian Organisation South Australian Research and Development
Institution (SARDI)
Australian Personnel Dr Martin S Kumar (Team Leader)
Dr Bennan Chen (Senior Scientist)
Completion date (original) February 2009
Completion date (revised)
Reporting period February 2006 – October 2006
In Australia: Administrative contact
Name: Position: Organisation
Trang 43.1 Project Implementation Progress
3 1.1 Key Highlights
• Technological and socioeconomic evaluation completed Report
submitted Report reviewed and accepted by CARD administration
• Clam culture in ponds (production) experiments involving prawn farm effluent and influent is progressing well
• Clam and prawn polyculture experiments is progressing well
• Preliminary experiments on clam spat production produced encouraging results
• Hatchery infrastructure established for spat production trials
3.1.2 Key outcome
a) Socio economic study completed
• Due to pollution as a result of poor water and nutrient management in the pond, shrimp culture is threatened with disease outbreaks Production cost is increasing
and profitability is being reduced due to the use of more chemicals, lime,
probiotic, etc for water and disease management
• Banks are reluctant to extend capital due to inconsistent aquaculture production due to unreliable culture technique in the case of clam culture Similarly banks are hesitant to provided loans for shrimp culture because of the high risk due to disease out break
• Lack of clam seed due to technology gaps is a major constraint, limiting the growth of clam farming development
• Although there is a ready market for clam, the middlemen exploit the farmer and generate a low price, which results in a low profit margin for the farmer Farmers indicated the need for cooperatives to play a major role in marketing
b) Production experiments made excellent progress Significant progress has been made
in this section Preliminary results from production experiment indicated that clam can be successfully cultured in ponds This is the very first successful production of clam in ponds carried out in Vietnam Although the experiment is still in progress, the
preliminary results indicated good clam growth and survival rate
C) Initial trials of spat production completed and encouraging results obtained
4 Introduction and Background
A summary of the project objective, outputs expected and approach and methodology
4.1 Objective
• The objectives of this project (027/05VIE) include the following:
• To develop and extend the clam culture technology (hatchery and
Trang 5environment management using clam aquaculture to improve prawn farm effluent utilisation
4.2 Outputs Expected
In accordance with expected output proposed, the fist six months were focused on following aspects related to achieving the development of clam production
technology
and hatchery operational procedure
• Infrastructure establishment for clam production trials in ponds
• Construction of lab facilitates for spat production experiments
• Clam production in ponds started
• Initial experiments on spat production started
• Completion of Socioeconomic survey
Above mentioned activities were completed as per the proposed logfram
4.3 Methodology
Two visits by Australian Project Leader and scientists (one in April 2006 and the other August 2006) enabled to undertake major review of the project methodology, implementation strategy and resource and progress evaluation Scientific approach has been refined for implementing appropriate methodology for the experiments The advantages are:
• Incorporate information from preliminary research results into the
following experimental design
• Clear scientific comparisons are possible
• Avoid duplication of activities
• Ease of management
• Efficient use of resource
4.3.1 Summary for amendments and clarifications
• Clam culture experiments
a) It was decided to exclude the objective of determining optimum size from the first three experiments (Polyculture of Clam and Prawn, Clam culture in prawn farm
effluent, Clam culture in prawn farm influent) as this could be done in other two
experiments where objective of determining substrata will not be included The
experiments would instead now focus on the following two objectives:
i Determine suitable substrata
ii Determine optimum stocking density
b) Removal of Substrate Experimental Objective from the rotational clam culture in prawn farm and intertidal clam culture Experiment is recommended The Rotational Clam Culture experiment will instead focus on the following two objectives
i Determination of optimum size
ii Determination of optimum density
Rotational clam culture prawn has to wait until September 2006 During this period
Trang 6of degree of risk, local support and collaboration, resource availability and degree of management difficulty Also the areas selected for the experiments are well known for
clam occurrence
d) Standardisation of sampling and measurement methods for all experiments to reduce data collection error was advised Due Standardisation of methods for measurement and use of measuring equipment, random sampling / sample selection from ponds, and rotational roster for data collection staff; Determination of sampling differences between staff was established
• Hatchery Experiments
Based on the preliminary results from the hatchery experiments the following sections
revised and refocused
i Brood Stock Conditioning
ii Breeding and Spawning techniques iii Larval Rearing / Culture Methods
iv Nursery (inclusive of Larval Settlement)
a) Experiments to determination of suitable temperature range for brood
stock conditioning will be further focused in the next experiment
b) Salinity Experiment to Hatchery Larvae Rearing Experiment A Salinity
Experiment to investigate the effect of salinity on growth and survival Each of 6 salinity concentrations between 10PPT and 35PPT were stocked with
25,000 larvae and measured for growth and survival rates until pediveliger
or late-umbo development stage (approximately 10 days)
c) Conduct of two larvae culture systems for comparison, in the larvae stocking density and water change component of the Larval Culture Experiment:
• Option one: the experiment will focus on larvae stocking density (with 3 level: 5 –
10 – 15 larvae/ml) with flow-through water system
• Option two: the experiment will focus on larvae stocking density (with 3 level: 5 –
10 – 15 larvae/ml) with water change every 24 hour, 36 hour and 48 hour
The two options were selected due to the need to determine the suitability of a single system for future experiments that would give a survival rate closer towards survival rates in literature
d) Introduction of a Nursery Experiment with the objective of determining optimal nursery conditions to maximize growth rate and survival rate of spat and juvenile of clam Specific objectives include:
• To determine feeding regime
Trang 7• To determine optimum stocking density
• To determine optimum substrate (artificial bottom and solid bottom/nylon mesh only)
• To determine nursery type (comparison of the hatchery through system with floating raft in booming pond systems)
system/flow- • This experiment will be described in greater detail below
e) Nursery Experiment specifications were finalized and the specifications were as follows:
• Method: The clam spats in their first week after settlement will be
transferred to nylon meshed screens for grow out Different mesh size of screens will be used for grading the spats during growth out period Following two methods are
proposed for spat grow-out
• Option 1: Indoor flow-through system (consist of holding tanks with size of 0.6 x
1.2 x 2.4 m): Water with algae (food) from the blooming pond (algal pond) will be fed into holding tanks containing spats and then returned back to algal pond This
continuous feeding will be carried out using electric pump
• Option 2: Outdoor pond system: In this system, spats will be reared in
the floating rafts kept within the blooming pond Water quality in blooming pond will be managed by adopting strict pond fertilization regime and pond management measures including water levels may need to be controlled to make sure that there are enough algae for feeding spat during the nursing period
The experiment will be focused on the following parameters:
1 Substrate Screen substrate Screen substrate
Solid substrate Solid substrate
Trang 82 Stocking density 150g/m3 200g/m3 250g/3 150g/m3 200g/m3 250g/3
3 Selected species of Species Species Species
algal culture (plastic
bags)
During the experimental period water quality parameters such as oxygen (6-8 mg/l), pH (8-8.5), ammonia <0.2 mg/l and water flow rate (30 ml/minutes/g of spat) will be maintained Density (biomass) of spats considered for the
experiment are: 150g live weigh/m3, 200g live weigh/m3 and 250g live weigh/m3
(volume of tank units is 2 m3 with 10 screens holding)
The holding tanks will be drained and cleaned each every two days, in this time the spat holding screens be also cleaned
All treatments will be carried out in triplicates The growth and survival rate of spats will
be recorded weekly along with grading
5 Progresses to Date
5 1 Implementation Highlights
5.1.1 Socio-economic study
Initial phase socio economic study completed The report accepted after the review
profitable despite a low production rate However, clam culture has the disadvantage of mainly relying on capture of seed source from the wild At the same time, due to
disease outbreak in the prawn farming sector as a consequence of water deterioration, there has been an overall reduction in aquaculture production Clam is recognized as a water cleaning machine(filter feeder), thus water quality will be improved if clam can be incorporated into the shrimp farming system Therefore integrated clam and shrimp culture would reduce risk through better pond water quality management, and has the potential to improve shrimp and clam production
Banks are reluctant to provide capital funds to the clam industry due to
inconsistent production and unreliable technology The shrimp farming sector
suffers a similar fate because of it’s high risk due to disease outbreak
Currently the clam industry is restricted to tidal flats In order for the clam industry to grow, clam technology for ponds must be developed, as there are limited tidal flats available for clam culture
Farmers received low prices for clam due to exploitation by middle men Cooperatives need to play a major role in marketing the clams
Shrimp and clam culture systems are seen as the backbone of the coastal community Clam culture is making more profit than shrimp, due to less capital cost and reduced risk It’s successful expansion will definitely improve the family income and living
standards for the people in the provinces
Trang 9• Key Results
a) Technology Issues
• Lack of Seed
• Lack of Clam Culture Method
• Lack of technical information
• Lack of information on species
• Lack of information on Polyculture of Clam and Prawn
b) Social factors
• Suitable education level of farmers (>88% secondary and above education) • High levels of attendance of aquaculture training (86%)
c) Economic Issues
• Finances from Banks and other Lending Institutions
• Funding from the Vietnamese Government
• Middlemen Margin Affecting Profits
• No Support Role by Cooperatives
• Key outcomes and Recommendations
• Clam culture can act to remediate the impacts of prawn farming so as to
increase sustainability of prawn farming in Vietnam
b) Recommendations
• Should develop hatchery technology
• Should develop grow-out and production technology
• Development of a business model to enable implementation by farmers
• Cooperatives and government should help in the marketing of Clam culture and Clam consumption
5.1.2 Production Experiment
Establishment of infrastructure and part of the results were included in this
section Experiments are in progress and complete results will be reported in
the next report
5.1.2.1 Infrastructure
a) Effluent and Influent pond systems set up in Thanh Hoa
Trang 10An effluent system for two treatments – bottom treatment, there are 9 ponds for 3
triplicates of substrata such as sand bottom, clay-sand bottom and clay bottom and
Density treatment, there are 9 ponds for 3 triplicates of density levels (90clams/m2,
120clams/m2 and 150clams/m2 ) comprised of a total of eighteen 9m2 ponds were set up
in Thanh Hoa Province (Fig 1) An influent system built (similar to effluent) and
experiments is being conduced the same as treatment included in effluent (Fig 2)
b) Clam and prawn polyculture An polyculture system for one treatment – Density
treatment: there are nine 50m2 ponds for 3 triplicates of density levels such as
60clams/m2, 90clams/m2 and 120clams/m2 This experiment also set up in Thanh Hoa Province
Fig 3 Density – Influent / Effluent System: project staffs are checking growth rate of clam
in pond
.c) Results obtained so far Since this experiment is in progress, results presented here only up to September 2006 Analysis will be undertaken after the completion of the
experiments A comprehensive analysis and discussion and conclusion will be included
in the next report
Trang 11Fig 4 Clam samples from the pond culture
• Density Experiment Growth Rate
During the initial phase of the experiments (when animal size is relatively small) the
growth rate appears to be similar in all three density treatments However, the growth difference became prominent as animal grow bigger Final data analysis and the results will be discussed in the next report This experiment is not yet completed
Figure 5 A to 5D show result of clam growth rate from influent pond system with
different stocking density
Growth rate (height) of M lyrata culture in influent pond by
Density Size of clam (in mm)
22.00 21.00 20.00 19.00 18.00 17.00 16.00 15.00
Days to culture
Figure 5 A Growth rate (Height) of M lyrata culture in Influent Pond, by Density
Trang 13fluent pond by Density
0 15304560
Days to culture
Figure 5 B Growth rate (Width) of M lyrata culture in Influent Pond, by Density
Growth rate (thickness) of M lyrata culture in influent pond by Density
Days to culture
Figure 5C Growth rate (Thickness) of M lyrata culture in Influent Pond, by Density
Growth rate (weight) of M lyrata culture in influent pond by Density
0 15304560
Days to culture
Figure 5 D Growth rate (Weight) of M lyrata culture in Influent Pond, by
Density Figure 6A to 6D show result of clam growth rate from influent pond system with different substrate
Growth rate (height) of M lyrata culture in
influent pond, by Substrate
Trang 140 15304560
Days to culture
Figure 6 A.Growth rate (Height) of M lyrata culture in Influent Pond, by Substrate
Growth rate (width) of M lyrata culture in influent pond, by Substrate
0 15304560
Days to culture
Figure 6 B Growth rate (Width) of M lyrata culture in Influent Pond, by Substrate
Growth rate (thickness) of M lyrata culture in influent pond, by Substrate
0 15304560
Days to culture
Figure 6 C Growth rate (Thickness) of M lyrata culture in Influent Pond, by Substrate
Growth rate (weight) of M lyrata culture in
influent pond, by Substrate
Trang 15Days to culture
Figure 6 D Growth rate (Weight) of M lyrata culture in Influent Pond, by
Substrate
Figure 7A to 7D show result of clam growth rate from effluent pond system with
different stocking density
Growth rate (height)of M lyrata culture in
effluent pond, by Density
0 15304560
Days to culture
Figure.7A Growth rate (Weight) of M lyrata culture in effluent Pond, by Density
Growth rate (width)of M lyrata culture in effluent pond, by Density
0 15304560
Days to culture
Figure.7B Growth rate (Width) of M.lyrata culture in effluent pond, by Density
Growth rate (thickness) of M lyrata in effluent
Trang 16Growth rate (weight) of M lyrata culture in effluent pond, by Density
Grow rate (height) of M lyrata culture in
effluent pond, by Subtrate
0 153045 60
Days to culture
Figure.8A.Growth rate (height) of M lyrata in effluent Pond, by
Substrate
Development of clam culture for improvement and diversification of livelihoods of the
poor coastal communities in Central Vietnam
Growth rate (width) of M.lyrata culture in
effluent pond, by Substrate
Trang 170 153045 60
Days to culture
Figure 8B.Growth rate (width) of M lyrata in effluent Pond, by Substrate
Growth rate (thickness) of M.lyrata culture in effluent pond, by Sustrate
0 153045 60
Days to culture
Figure 8C Growth rate (thickness) of M lyrata in effluent Pond, by substrate
Grwoth rate (weight) of M.lyrata culture in effluent pond, by Substrate
5.1.3.1 Brood stock Conditioning
a) Infrastructure establishment
A triplicate system for two treatments – Sand bottom and Solid bottom was set up at ARSINC This comprised of a total of six 200L tanks in a recirculation system at
Trang 1828.25°C
Fig 9 : Recirculation System (Constant Temperature) at ARSINC
A triplicate system for two treatments – Sand bottom and Solid bottom was set up at ARSINC This comprised of a total of six 400L tanks in a recirculation system with an automated heating system to increase the temperature from 26°C to 30.5°C
b) Conditioning methods
Gonad Development using stable temperature and gradually increasing temperature procedures were used in brood stock conditioning experiments The experiment
conducted in a stable temperature system, water temperature was constant at
28.250C in 10 days The experiment conducted in a Increasing temperature system,
Trang 19water temperature was increasing from 260C up to 30,50C in 10 days
c) Key Results
Figure 11 and 12 show the status of gonad development in two experimental conditions
In stable experimental condition figure 11 shows that gonad of clam is developing at Stage but the development of egg cells is not uniformly progressing Fig 12 (increasing temperature) also shows that gonad of clam is developing at stage IV but the
development of egg cells is not uniformly progressing
Fig 11 gonad development under stable temperature 28.250C
Fig 12 Gonad development under increasing temperature 260C to 300C
• Stable Temperature Experiment
Minimum gonad development was observed for both the sand and solid bottom experiments at 28.5°C (Figure 11) An average overall decrease in gonad weight of 0.12g was observed for sand bottom stable temperature treatment and a decrease of 0.19g was observed for solid bottom treatment
Trang 20There was no significant variation in soft weight of the samples, with a maximum variation of +/- 0.53g in the sand bottom treatment and a maximum variation of +/- 0.19g for solid bottom stable temperature treatment
Gonad Development of Clam (M.lyrata ) in Stable Temperature System
Weight (in gram) 2.5
T imes (in Days) to check Gonad Development
Figure 13 M lyrata Gonad Development at Stable Temperature, Sand and Solid
Bottom (Breeder Conditioning in Hatchery Experiment)
• Increasing Temperature Experiment
In random sampling of sand bottom and solid bottom environments for Increasing
Temperature treatments (26°C to 30.5°C), 15 samples were taken from each
environment per sampling Total weight (including shell), soft weight and gonad
weights were measured for variations in grams to two decimal places Similar to the previous experiment, an increase in ‘soft weight’ would correspond to gonad
development (Kraeuter and Castagna, 2001) An average overall decrease in soft
weight of 0.47g was observed for sand bottom and a decrease of 0.40g was observed for solid bottom
No gonad development was observed for both the sand and solid bottom experiments for the range of 26°C to 30.5°C (Figure 14) An average overall decrease in gonad weight of 0.12g was observed for sand bottom stable temperature treatment and a decrease of 0.19g was observed for solid bottom treatment
There was no significant variation in soft weight of the samples, with a maximum
variation of +/- 0.53g in the sand bottom treatment and a maximum variation of +/- 0.19g for solid bottom stable temperature treatment
Gonad Development of Clam (M.lyrata ) in Increas ing Temperature System