| |
Aquaculture 164 1998 117–133
Nutrient budgets in intensive shrimp ponds: implications for sustainability
Simon J. Funge-Smith ), Matthew R.P. Briggs
( ) Stirling Aquaculture Asia , P.O. Box 32, Kao Seng, Songkhla 90001,
Thailand
Abstract
Serious production losses have occurred in shrimp producing countries
around the world,
principally due to poor rearing environments and pathogenic disease. In
response to this, shrimp
farmers are changing their culture methods. To understand the source and
sink of nutrients which
affect pondwater quality and effluent impact, the nitrogen, phosphorus
and solids budget have
been constructed for water exchange systems. These budgets reveal the
contribution of the pond
bottom soil to the accumulation of sediment and phosphorus and its potential
contribution of
nitrogen to the pond system. A survey of shrimp farm water quality and
management practices in
southern Thailand has also been completed. This reveals a high proportion
of farms using low
water exchange methods of shrimp culture but without the ability to maintain
suitable water
quality in the production ponds. Shrimp production in these systems is
variable due to high
incidences of disease and slow growth rates. The pond processes that might
cause this are
suggested and potential methods for their amelioration are discussed.
Alternative culture systems
such as lined ponds, low salinity rearing and recirculation farms are
described in relation to their
potential for remediating problems within the shrimp culture industry.
q1998 Elsevier Science
B.V. All rights reserved. click here to print 
Keywords: Shrimp; Production systems; Solids and nutrient budgets
1. Introduction
The rapid increase in world cultured shrimp production and its equally
rapid decline in some
countries like Ecuador, China and Indonesia Shrimp News International,
199
has left environmental, social and financial problems in its wake. This
has not prevented
) Corresponding author. Tel.: q66-74-324-475; fax: q66-74-324-475; e-mail:
aquacon@t-rex.hatyai.inet.co.th
.
0044-8486r98r$19.00 q 1998 Elsevier Science B.V. All rights reserved.
top
back
PII S0044-8486 98 00181-1
( ) S.J. Funge-Smith, M.R.P. Briggsr Aquaculture 164 1998 117–133 118
the development of new stretches of coastline for shrimp culture and the
further
intensification of existing areas. Shrimp farming has the capacity to
dramatically
transform coastal areas. Extensive farms have an enormous requirement
for land and the
development of intensive culture practices increases nutrient impacts
on the local coastal
environment. Alongside environmental changes such as eutrophication, salination
and
land use changes, are attendant social transformations Lin, 1989; Chua
et al., 1989;
Csavas, 1993; Liao, 1990; Macintosh and Phillips, 1992; Panvisavas et
al., 1991;
Primavera, 1991, 1992, 1993, 1995 . These can be both positive and negative;
the
increased income into traditionally poor coastal areas must be balanced
against loss of
job diversity, loss of independence, rising prices and growing inequity
between farmers
and non-farmers Chong, 1990; Masae and Rakkheaw, 1992; Nuruzzaman, 1996;
Primavera, 1993,1995 .
Once changes have occurred frequently irreversibly , it is often important
to
maintain the industry in some form. Collapse of shrimp farms leaves nothing
for the
inhabitants of an area since agricultural land and mangroves are degraded
and often,
former farmers are left with considerable debt. This leads to loss of
land and an inability
to return to their original lifestyle. There is a pressing need for the
development and
dissemination of a range of shrimp culture systems that are both environmentally
and
economically sustainable.
Typically the pattern of production from a shrimp farm is that of an initial
‘honeymoon period,’ characterized by success and good production followed
by gradual
decrease in yields over successive crops. Depending upon a wide range
of factors,
decreased yields are manifested as reduced growth, higher FCR, and disease
outbreaks
that require emergency harvesting. The worst case is that of complete
mortality of stock
and this is being encountered more frequently with the increasing incidence
of extremely
pathogenic viral diseases . Although there are now several primary pathogens
viral of shrimp,
the majority of shrimp disease is caused by secondary pathogens that are
able to invade shrimp
already stressed and weakened by a poor quality rearing environment. A
shrimp that is stressed
does not grow rapidly, principally due to reduced feeding and delayed
moulting. It is
important to maintain a healthy rearing environment for the shrimp to
maximize
production potential and minimize the risk of opportunistic disease.
The viral type diseases such as ‘yellowhead’ YBV and ‘white spot’ SEMBV
disease appear to be transmitted via influent water and intermediate crustacean
host,
respectively. There is now some evidence that ‘white spot’ can also be
transmitted
through the post-larvae Flegel et al., 1996 . These diseases cannot necessarily
be
prevented by the provision of a good quality rearing environment, although
a poor
environment certainly will increase susceptibility. Yellowhead disease
already appears to
be decreasing in pathogenicity from that of a primary to opportunist type
pathogen. In
1993, only 0.05% of the tiger shrimp Penaeus monodon carrying the virus
were
asymptomatic, now this figure has increased to 60% Flegel et al., 1996
. Therefore,
environmental quality will have a more significant effect than before.
The response of
Thai farmers to these two viral diseases, has been to reduce water exchange
in an
attempt to prevent transmission between farms and ponds. This practice
has generated its
own problems which will be discussed later.
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 119
In order to better understand the link between environmental quality and
production,
it is important to understand some of the underlying relationships between
the two. This
knowledge allows the significant processes occurring in different culture
systems to be
identified and suitable management strategies to be derived. click here
to print 
back
2. Environmental processes in shrimp
culture systems with water exchange
The two significant components of the pond environment are the pond water
and
sediments which interact continuously to influence the culture environment.
Pond
sediments can be further divided into the pond soil component the pond
bottom and
walls and the accumulated sediment component the sludge that accumulates
on the pond bottom
during culture Briggs and Funge-Smith, 1994 . Pond management activities
are a third external factor
which influence the culture environment.
Management activities include feeding, use of aerators, water exchange
and liming Fig. 1 .
The original method of intensive shrimp culture in Thailand involved relatively
high y2.
y1 y 1. stocking densities 50–100 m , high production 6–12 t ha crop ,
high feeding
rates FCR 1.8–)2.0 and high rates of water exchange up to 5–10% per day
towards
harvest time . Water quality management was achieved by a combination
of flushing the
pond with clean seawater and management of the phytoplankton bloom by
assessment of
pond colour. Water exchanges were frequent, especially in the latter half
of production.
Accumulated sediment was known to be undesirable and was removed between
cycles.
Experience has taught farmers that inadequate sediment removal would cause
water
quality problems early in the subsequent crop. Due to the high flushing
rates and
naturally high levels in seawater, the alkalinity of the pondwater was
not considered
important and no attempt was made to control pH. Oxygenation of the pond
during the
Fig. 1. Water quality interactions and management activities in intensive
shrimp ponds.
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 120
day was largely achieved by the phytoplankton bloom giving rise to supersaturated
oxygen 130–150% and high pH 8.3–9.5 by the afternoon. This oxygen concentration
would gradually diminish overnight and aeration would be started during
the very early
morning to prevent critically low levels. Aeration was usually suspended
during the day
to save power costs and in the belief that it was unnecessary. Feed management
in Thai
intensive ponds is achieved through the use of lift trays which are checked
regularly to
assess if shrimp are feeding. On larger farms, shrimp growth was recorded
to cross
check the feeding rates and also to estimate potential production. click
here to print 
top
back
3. Nutrient and solids budgets
A study of this ‘open’ type system was performed in southern
Thailand using shrimp
ponds constructed on clay soils Briggs and Funge-Smith, 1994 . Budgets
were derived
for solids, particulate organic matter, nitrogen, and phosphorus. Three
different types
of pond were investigated: one-year and two-year old ponds stocking density
50–60 m and
one-year old ponds with higher stocking density 80–100 m .The solids
budget Fig. 2 shows
that erosion of pond soil was the major source of both solids 88–93%
and organic matter 40–60% in the pond.
The feed applied to the
pond was a significant source of organic matter 31–50% but contributed
little solids
4–7% to the system. This is important since the feed component is
also an indication
Fig. 2. Total and organic solids budgets for intensive Thai shrimp ponds
Funge-Smith and Briggs, unpublished data .
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133
121
of the faecal contribution by the shrimp. Influent water is a major source
of sediments in
extensive systems Boyd, 1992 , but contributes only 2–3% of solids
in intensive
systems because stirring generates more endogenous solids. The organic
contribution of
the influent water was significant 7–13% , but less so than feed
and soil erosion.
Shrimp culture ponds are effective sedimentation areas Boyd, 1992 such
that the bulk
of the solids introduced to the system endogenously and allocthonously
remain in the
pond as accumulated sediment 91–94% . This accumulated sediment
was the sink for
58–70% of the organic matter in the system. Routine water exchange
accounted for 4%
of solids discharge and pond drainage for a further 3%. The organic content
of these
discharged solids were 13% and 9% respectively. The shrimp were a relatively
minor
component in the whole system, accounting for just 0.7% of the solids
and 6.1% of
organic matter. The important consideration that emerges from these budgets
is that the character of the pond soil will have a significant effect
on the water quality and production of a
shrimp pond. Depending upon initial compaction and organic content, the
soil will affect
the organic matter and solids of the system. In the case of mangrove soils,
organic
content can be two or three times that of clay soils e.g., rice paddy
. Sandy soils are the
opposite containing little organic matter. It is frequently observed that
starting phytoplankton
blooms in these ponds is difficult and they are liable to crash frequently.
Ponds
with sandy soils also suffer from high seepage rates causing problems
as organic
material is drawn into the soil matrix where anaerobic decomposition can
occur. After
one or two crops, production losses occur due to seriously deteriorated
pond bottom
conditions Funge-Smith and Stewart, 1996 .
The organic component of the accumulated sediment is a mixture of pond
soil
organic content and detrital material. This detrital material is composed
of sedimented
organic material from plankton, shrimp faeces and uneaten feed. The character
of the
accumulated sediment is therefore dependent upon culture intensity, pond
soil organic
content, and water exchange practices. Problems associated with the pond
bottom and
accumulated sediment occur when excessive organic material builds up causing
release
of ammonia, organic sulphur compounds, and, in cases of extremely high
organic matter
and acidic soils, hydrogen sulphide Avnimelech, 1996; Lin, 1989; Fast
and Lannan, 1992;
Wang and Fast, 1992 .
Inadequate cleaning of the pond bottom between crops leaves organically
enriched
sediment across the pond bottom. Due to its non-compacted nature, this
sediment is
easily suspended by the action of aerators during the next production
cycle. The organic
matter released from this sediment tends to stimulate very heavy phytoplankton
blooms
in the first month of production. Because of this, old ponds in Thailand
are rarely
fertilized to stimulate phytoplankton bloom. Non-removal and respreading
of the
accumulated sediment over the pond bottom has been proposed since the
increase in
organic content can be slight. However, experience of poorly cleaned intensive
ponds
suggests this is unwise. Non-removal of sediment might be a viable alternative
if ponds
were farmed less intensively, fallowed for longer periods, and the sediment
compacted.
The solids discharged from the ponds form a minor but significant part
of total solids
in the system. The total discharge of organic matter in the effluent was
4.8 t hay1 and
the total solids approximately 12.6 t hay1. Trapping these solids as they
are discharged
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133
122
represents a major problem in reducing shrimp farm impact on the surrounding
environment. The suspended solids in a shrimp pond have a different character
from the
sedimentable solids. Frequent cessation of aeration during the production
cycle allows
the heavier soil particles to settle and form the accumulated sediment.
Phytoplankton,
bacteria and the organic particulate fraction are not easily sedimented
due to natural
buoyancy, or having a specific gravity close to that of seawater Rubel
and Hager,
1979 . In trials on shrimp pond waters one hour settlement achieved 22–44%
settlement
of suspended solids. There was no significant difference between settling
times of 1, 2
and 3 h Fig. 3 . Thus, the use of settling ponds for removal of this fraction
is bound to
be ineffective unless enhanced sedimentation is practiced e.g., flocculation
. Harvest
effluents are more easily settled because they are a mixture of resuspended
accumulated
sediment and the suspended solid fraction of the water.
The actual amount of nutrients assimilated into shrimp biomass is a small
fraction of
the total applied as feed Table 1 . Only 18–27% of nitrogen and
6–11% of carbon
applied to the pond was assimilated thus there is considerable wastage
as nutrients are
either incorporated into plankton biomass, volatilized or trapped in the
sediments.
The nitrogen and phosphorus budgets reveal in more detail, the sources
and sinks of
the organic components in an intensive shrimp pond Fig. 4 Fig. 5 Briggs
and. Funge-Smith, 1994 .
Applied feed accounted for 78% of the input of N to the ponds Fig. 4 .
Erosion of the pond soils,
whilst a major contributor of solids, accounted for only 16% of N added
to the system.
Other minor contributions were influent water 4% and fertilizer, rainfall
and postlarvae 2% .
The sinks for nitrogen were the sediments 24% , harvested shrimp 18% ,
and discharged water 27% . This leaves approximately Fig. 3. Settlement
of suspended solids from shrimp pond waters
Funge-Smith and Briggs, unpublished data. ( ) S.J. Funge-Smith, M.R.P.
BriggsrAquaculture 164 1998 117–133 123
Composition of shrimp and feed showing assimilation and loss to environment
Funge-Smith and Stewart,. 1996 a Nutrient Proximate analysis % dry weight,
Composition Assimilation at FCR 1.65–2.40
of 1 kg dry Feed Shrimp grams % y1 feed g kg y1 kg non-assimilated .
A 1 kg of dry feed at FCR 1.65–2.40 produces 113–165 g dry
weight shrimp .
30% of the nitrogen unaccounted for which is assumed to be N lost to the
atmosphere as
N or ammonia. This volatilization of nitrogen emphasizes the significance
of microbial 2
decomposition processes in ponds, especially bacterial conversion of nitrogen
com-
pounds principally nitrate to N Fry, 1987 . The high loading of nitrogen
in the pond 2
effluent highlights its potential impact on receiving waters. This loss
of nitrogen is also a
Nitrogen budget for Thai intensive shrimp ponds using water exchange adapted
from Briggs and Funge-Smith, 1994 .( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture
164 1998 117–133 124
Phosphorus budget for Thai intensive shrimp ponds using water exchange
adapted from
Briggs an Funge-Smith, 1994 wasted resource that could be incorporated
into the growth of other organisms.
The site of this bacterial activity is unknown—does nitrate conversion
occur principally in the sediments or in anaerobic microzones in the suspended
solids fraction? This question is
of considerable importance in the management of bacterial flora in shrimp
ponds.
The principal source of phosphorus in this system was the applied feed
51% Fig. 5 .
The 26% shortfall in inputs was assumed to be the eroded pond bottom.
None of
these ponds were new and previous cleaning had left old uncompacted sediment
on the
surface, which is easily eroded during the next cycle contributing phosphorus
to the
system. Effluent water still constituted 10% of P loss in the budget and
this is mostly
bound in the suspended solid fraction. Again, trapping of the suspended
solid fraction is
important to minimize impact. click here to print 
top
back
4. Potential solutions
Common problems in the open water exchange system include phytoplankton
crashes,
deteriorated pond bottoms and bacterial diseases. A phytoplankton crash
causes a
significant increase in ammonia in the water, a decrease in dissolved
oxygen and a rise
in organic material. This stressful situation, together with increased
bacterial concentrations,
often leads to outbreaks of vibriosis, Zoothamnion infections, and luminescent
Vibrio in the ponds. Traditionally, the only method for ameliorating this
problem was
high levels of water exchange Chanratchakool et al., 1995 .
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 125
Monthly water exchange rate % in open, semi-closed and closed shrimp production
systems
in southern Thailand 1993–1995 a b c Month Ranod–Hua Sai 1993 Chantaburi
1994
Southern Thailand 1994–1995. NACA 1994 .b Marsden 1994 . c Funge-Smith,
1996.
Due to deterioration of estuarine and coastal water bodies, many shrimp
culture areas
no longer have the clean seawater required for this method of culture.
This has led to
decreasing amounts of water exchange. One reason for the widescale adoption
of low
water exchange systems in Thailand has been the perception that water
exchange
triggered disease outbreaks. There is now substantial evidence that the
viral disease
yellowhead is transmissible in water and that white spot disease is introduced
via
crustacean intermediates during water exchange. The assumption that separating
the
production pond from external water inputs may prevent the introduction
of viral disease
has given rise to the ‘closed’ and ‘semi-closed’ culture systems in Thailand.
click here to print 
back
4.1. Closed and semi-closed systems
These systems operate by filling a pond and using a biocide to kill any
potential
vectors of viral disease mysid shrimp, white shrimp, swimming crabs, zooplankton.
The usual biocide used is calcium hypochlorite 60% wrw applied at 300
kg ha , but there
is increasing interest in the use of more specific organo-phosphate pesticides
due to the
effect of chlorine on the phytoplankton as well. After chlorination the
pond is limed and
aerated to disperse residual chlorine and stimulate the development of
phytoplankton bloom.
There is no water exchange in the first two months after stocking in these
systems,
although filling of the pond is necessary towards the end of the second
month. Depending upon
season and rainfall, evaporative loss can cause salinity to rise to an
unacceptably high level. To counteract this, freshwater is pumped where
available
although this has very serious environmental and social impacts if aquifer
water is used
Liao, 1990; Primavera, 1991; Csavas, 1993 . During the monsoon seasons,
rainfall is
sufficient to prevent high salinities. In the semi-closed system, limited
water exchange
commences during the second month of production. In the fully closed system,
the
farmers attempt not to change any water at all and merely add water if
necessary. Total
effluent loadings from systems employing any form of water exchange are
not significantly
different when compared with fully closed systems. The loadings in Table
3
represent those discharged as a result of water exchange, and do not account
for
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 126
Nutrient loadings as a result of water exchange activities Funge-Smith,
1996 .
Organic suspended solids accumulated within the system. In the case of
fully closed systems,
impacts are relatively small with respect to effluents, but the actual
rearing environment is stressful
as a result of high organic loadings within the ponds.
Low water exchange systems such as these are complete sinks for nutrients
and thus
there is no outlet for wastes during production except for discharge at
harvest Table 3 .
The nitrogen budget above shows that even in an open system water exchange
does not
result to a major loss of N 17% Fig. 4 . The lack of water exchange has
one
significant management problem, over-blooming phytoplankton. This has
always been a
problem since the phytoplankton eventually crashes and causes severe stress
to the
shrimp. One of the management methods currently employed is the killing
of the bloom
by the application of biocides usually BKC, formalin, glutaraldehyde,
calcium hypochlorite .
This is applied in the corners where phytoplankton density is greatest.
Aeration is suspended during treatment followed by vigorous aeration to
disperse the
chemicals and reduce the concentration to a harmless level. The dead phytoplankton
releases a great deal of ammonia and decomposes, forming a thick stable
foam on the
surface of the pond or sinks to be incorporated into the sediment. The
floating foam is
removed from the corners of the pond where it collects.
By virtue of their higher organic loadings, closed and semi-closed systems
appear to
encourage dinoflagellate and blue–green algae cyanobacteria blooms e.g.,
Gymno-dinium,
Peridinium, Gonyaulax, Coscinodiscus, Anabena, Oscillatoria . The dark
brown,
red or purple–black appearance of a pond is typical of such blooms and
are considered
to be stressful to the shrimp and undesirable in shrimp ponds.
Due to the high concentrations of ammonia often encountered in these two
systems,
3.0 mg l , it is vital to control of pH. Daily pH checks are often performed
and an
attempt is made to maintain pH between 7.8 and 8.4 during the day time.
Alkalinity
phenolphthalein method is also checked regularly. If alkalinity is considered
too low
dolomite is applied. If pH rises too high during the day some attempt
is made to reduce
the phytoplankton concentration. If alkalinity is too high, organic acids
such as acetic
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 127
acid are sometimes added to neutralize some of the carbonate. The requirement
for CO2
as a nutrient by the phytoplankton is well known, but the loss of bicarbonate
as a result
of acidification due to bacterial denitrification is rarely considered.
From the nitrogen
budget approximately 30% of nitrogen appeared to leave the pond in gaseous
form, therefore the bacterial activity required to achieve this must be
considerable. Due
to their low solubility, the addition of lime and dolomites to increase
buffering capacity
of pond water may not always be effective in controlling water buffering
capacity.
Use of formalin has increased significantly due to its biocidal effect,
acidity, and
capacity to combine with ammonia. Treatment of ponds with 10 ppm formalin
not only
kills phytoplankton when applied, but removes ammonia when dispersed.
Formalin also
contains formic acid so that pH is not elevated during treatment. The
use of BKC in this
respect has declined because of its high pH Chalor Limsuwan, Department
of Fisheries,
Thailand, personal comm. The use of bacterial remediation treatments is
also
in these systems in the belief that regular addition will help maintain
low ammonia concentrations,
reduce organic matter concentration, and improve the quality of accumulated
sediment in the
pond. Since monitoring of these two parameters is rarely performed, there
is little
evidence of any effect Funge-Smith and Stewart, 1996 . The addition of
carbon sources
to production ponds has yielded interesting results in terms of modification
of microbial
communities in ponds. Additional carbon sources sugar, molasses, cane
sugar, etc.
appear to increase activity of heterotrophic bacteria in ammonia removal,
but in what
form the ammonia is removed and whether this removal is sustained are
unknown.
Ideally ammonia would be de-nitrified to nitrate, subsequently converted
to nitrogen and
volatilized. This function is not performed by the bacteria usually present
in bacterial
remediation products. It appears that if sugar is not applied regularly
the bacterial
community is not sustained and ammonia can re-appear i.e., a bacterial
bloom crash .
Applications of sugar are approximately 3–5 kg hay1 per time and this
may last for
several days to a week. The carrying capacity of a closed or semi-closed
system appears
to be exceeded at approximately 100–120 days post stocking resulting in
stressful conditions,
slow growth and disease outbreaks. Growth rates are slower in closed systems
than open, with
harvest sizes of approximately 40–50 pieces. Harvesting is usually done
when
shrimp stop feeding or when farmers perceive that the shrimp are no longer
growing.
The slower growth rates and eventual overloading of the closed and semi-closed
systems
can be attributed to several causes. The build up of waste sediment releases
increasing
amounts of ammonia and organic matter. This in turn encourages heavy Vibrio
and
Zoothamnium numbers in the pond. The shrimp become stressed and therefore
become
more susceptible to these opportunist diseases. Phytoplankton bloom crashes
are frequent
in these systems and, whilst re-blooming is comparatively quick, there
is still a
period of stress to the shrimp. The control of accumulated waste in these
systems
is considered critical to the success of the closed system, as is the
effective cleaning
of the pond between cycles. This has resulted in very high water circulation
using aerators
in the production ponds to keep the feeding areas clear of detritus and
mud.
The solids budget above demonstrates that soil erosion is the most significant
source of solids input to the system, thus ( ) S.J. Funge-Smith, M.R.P.
BriggsrAquaculture
164 1998 117–133 128 heavy water circulation results in high sediment
accumulation and
increased suspended solids in the water. The heavy erosion of soil from
the pond bottom
and its combination with detritus and faeces is potentially a method by
which organic material
is removed from the pond system. By consolidating the highly organic detritus
in a low organic
sediment the rate of diffusion out of the sediment could be slowed down.
Many farmers
are all too aware of the problems with ammonia and disease they can cause
if this
sediment is disturbed i.e., when aerators are moved . Many farms employing
low water
exchange systems are still unable to maintain clean feeding areas due
to inadequate
water circulation or poor aerator position. Deep ponds )1.5 m are difficult
to
circulate using paddlewheels and airjet aerators have caused problems
with erosion.
Removal of accumulated sediment during production is an option Hopkins
et al., 1995
that is unknown in Thailand, although it shows great potential for lowering
organic
loading in these systems. The problem with removal of the accumulated
sediment is that
once it has accumulated it loses its fluid properties, becomes gel-like
and cannot be
pumped out. A second problem is too frequent pumping would require addition
of water
to the pond. click here to print 
top
back
4.2. Lined ponds
One method by which many problems of earthen ponds especially low water
exchange systems can be avoided is the use of pond lining. Full pond liners
bitumen
impregnated geotextile have great potential in separating the pond bottom
from the
water column at the Tinsulanonda Songkhla Fisheries College. This eliminates
soil
erosion and reduces the accumulation of sediment in the centre of the
pond, resulting in
a larger clean feeding area for the shrimp and quick but efficient pond
cleaning
typically 1–2 days with bulldozerrbackhoe for earth pond, 3 h with hose
for lined
pond . Very little waste is left in the pond after harvest and the dryout
time required for
earth ponds is not necessary. The characteristic of the small volume of
accumulated
sediment found in lined ponds is completely different for that of earthen
ponds.
Accumulated sediment in lined ponds is not consolidated 83% water vs.
62% water in
earth ponds , remains extremely liquid and can be easily pumped out of
the pond. The
lack of soil in the accumulated sediment of lined ponds causes it to have
a higher
w organic content 36% than in accumulated sediments of an earth pond ex-mangrove
x 13%. This high organic content is also reflected in the higher levels
of leachable
nutrients in the accumulated waste of lined ponds. The higher levels of
labile
Accumulated sediment analysis means"s.d. Funge-Smith, 1996
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 129
ammonia and dissolved reactive phosphorus in the lined pond waste have
implications
for sediment management since these nutrients can act as fertilizers and,
if in excess,
stimulate overblooming in the pond. On the other hand removal of these
nutrients can
destabilize the phytoplankton bloom resulting in high water transparency.
The former
situation is becoming usual at the Fishery College. The high organic content
of
accumulated sediment from lined shrimp ponds can also be used as fertilizer
after
desalting Bergheim et al., 1993
Despite the promise that lined and partially lined ponds can improve water
quality,
production from these systems has not been fully convincing, possibly
because new
management techniques are required. One reason for the observed cannibalism
and
occasional high FCR in lined ponds, is the tendency for feeds to be rapidly
carried to the
centre of the pond with water circulation. The contribution of the pond
soil and detrital
feeding to shrimp nutrition and growth is uncertain in intensive ponds,
lined ponds
might limit the availability of some nutrients to the shrimps. By forming
a barrier
between the pond soil and the water, anaerobic conditions develop beneath
the liner.
Adequate drainage must be provided to allow exit of seepage water. Gas
formation
below the liner can cause it to float so weighting is also required typically
concrete
strips or fencing posts . If pond soil is potential acid sulphate, the
conditions below the
liner can become extremely toxic. In such situations, sand can be applied
between the
soil and liner to facilitate drainage. Care must be taken to avoid seepage
from adjacent
unlined ponds and canals.
The principal drawback of liners in shrimp culture ponds is their high
cost and
relatively short service life. The lining material for ponds can cost
between $1–3 m2 ,
and service life can be as short as 2 crops. More expensive liners last
longer, but care
must be taken to avoid deterioration from exposure to sunlight if there
is extended time
between crops. Ponds should be full of water even if there is no stock.
Disposal of old
lining materials will become a problem if widescale adoption occurs, since
burning them
appears to be the most likely method. click here to print 
back
4.3. Recirculation and integration
Recirculating farms exist in Thailand but appear to have production problems
associated with salinity and disease transmission within the farm. In
fully recycled
farms, water is recirculated through production ponds and into settlement,
treatment and
storage reservoirs. If disease enters this system, it is very difficult
to isolate and treat
parts of the system. The trend now is to use a limited water exchange
system for the
production ponds, replacing water loss from treated reservoirs. This allows
individual
ponds to be controlled if there is a disease problem. The large water
area required for
these farms causes high salinity in the dry season, such that recirculated
farms are filled
during periods of low salinity. Salinity can then increase through the
dry season until
harvest. Second cropping is difficult since low salinity water is not
available, but losses
from the system can be replaced with full strength seawater, and by the
end of the
second crop lower salinity water is available. Systems such as this can
only be used
when the farm is situated in estuaries or where river water is available.
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 130
Integration of other species such as fish, molluscs and seaweeds in the
recirculating
system is not possible until the problem of heavy solids loading in effluent
water can be
resolved. There are additional engineering problems when the farm cycle
of four to five
months is not sufficient to produce a crop from the integrated species.
Tilapia’s nest
building activity can disturb sediments, and the pseudofaeces from bivalves
can cause
self-fouling and severe sediment problems in areas where they are cultured.
Plankton
grazing fish species can be used to control phytoplankton. Mangrove oysters
require a
diurnal tidal rhythm to grow effectively and cannot be flooded 24 h a
day. Seaweeds
need cleaning every other day by shaking off the adhering sediments. Both
bivalves and
seaweeds are extremely effective at removing solids from the water, bivalves
by
filtration and seaweeds by trapping solids in the mucilage on the thallus
surface. It
appears that the obstacles to successful integration lies in the solution
of some
engineering problems and finding the potential markets for these low value
species. It is
worth noting that if pond lining becomes widespread the lower inorganic
solids loading
may enable successful integration of other species. click here to print
top
back
4.4. Low salinity
Recently, low salinity farms have increased in number dramatically due
to the
establishment of closed system culture techniques. Clay ponds inland are
filled to one
third of its capacity with sea water that is transported from the coast.
The ponds are then
filled with fresh water and the resulting salinity is approximately 5–10‰.
Alternatively
farms on inland estuaries that have access to very low salinity water
can also now farm
shrimp. The problems of these farms are similar to the closed system ponds
with respect
to sediment accumulation and heavy phytoplankton blooms although the higher
salini-
ties favour dinoflagellates and low salinities tend to give rise to blue–green
algae . Low
salinity ponds do not have a problem with increasing salinity, but if
culture takes place
during a season when there is significant amount of rainfall, salinity
will decrease in the
ponds and give rise to problems. If shrimp of appropriate age, then they
can tolerate
salinities as low as 2‰ but this is not advisable for small animals. Seasalt
placed in bags
in front of the aerators can slightly increase the salinity if necessary.
Buffering in this
system is low due to low salinity and limes or bicarbonate can be used
to boost this.
Generally growth rates are very fast in these systems and FCR can be as
low as 1.3–1.4
Pornlerd Chanratchakool, Thai Department of Fisheries, personal comm.
. However,
production cannot usually be extended beyond 90–100 days, so shrimp are
still
y1 . harvested when they are still quite small 50 pieces kg . The occurrence
of blue–green
algae may result to bad smell or poor taste of the shrimp but this rarely
happens.
Middlemen often complain about these to be able to buy at lower price.
click here to print 
back
4.5. The future?
The range of shrimp farming systems and techniques currently available
offer
solutions to many of the problems within the shrimp industry. These solutions
can
improve the environment both within and outside the rearing pond environment.
The
biggest threat facing the shrimp culture industry is its size and the
density of farms in
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 131
shrimp culture areas. The high intensity production and high concentration
of animals
offer the ideal environment for the evolution of new diseases especially
viruses .
Although we may be better able to control the environment within a farm,
there is
still constant threat of disease introduction from external sources. Viral
disease transmission
via postlarval transfer is currently acknowledged to be a possible route
of
introduction to farms and between shrimp producing countries. It is important
therefore,
to control broodstock and postlarval transfer between countries. Research
on captive
breeding of P. monodon will allow genetic improvement of stocks and also
the
production of disease freerhigh health stocks. The reduction of pathogenicity
of viral
diseases is likely to be more rapid than our ability to produce disease-resistant
shrimp.
However, screening postlarvae and water to prevent entry of disease can
be an effective
method in limiting transmission. The production of healthy postlarvae
is of paramount
importance in many countries due to broodstock shortages and poor post-larval
quality
and in itself is still a major economic and production constraint.
Within areas with established shrimp farms, it is important to ration
the flow of
influent and effluent water NACA, 1994 . This is essential if disease
is to be excluded
from farms and good environmental quality maintained. Rationing can take
the form of
shared inlet and outlet canals, effluent settlement and storage and settlement
of harvest
effluent. Waste removal from ponds, though largely innocuous although
saline , can
seriously degrade water bodies if dumped on land.
Since most shrimp diseases have a strong environmental component in their
expression
it is important that shrimp farmers are made aware of the effect of their
actions on
the pond environment and on the environment surrounding their farms. This
is of great
importance to the industry since regulation through policing is rarely
effective due to
lack of resources and farmer resistance. The dissemination of reliable
information to
shrimp farmers is vital since the principal source of information regarding
culture
methods are the retailers of feed and chemicals. The vested interest of
these commercial
organizations often results in inappropriate culture practices.
Aquaculture production methods that rely heavily on chemical intervention
can be
viewed as stressful and therefore undesirable. Intensive systems utilizing
high rates of
feed application are often undesirable due to the requirement for close
control of the
pond environment. This is rarely achieved and thus the system is wasteful
and often
susceptible to disease. The development of semi-intensive shrimp farms
is often seen as
the most sustainable method of shrimp farming. However, the land requirement
of this
system can result in the disruption of huge areas of coastal zone. In
some countries, a
more limited, but more intensive form of shrimp culture might be appropriate.
Unfortunately,
the investment in such systems is often prohibitive and the skills required
to run
such farms are lacking.
Shrimp farming is now a feature of many tropical coastal environments
and affects all
communities dwelling in the vicinity. Due to the dramatic effect of shrimp
farming on
coastal economies, collapse of farms in an area can seriously disrupt
local economies.
This is often due to the loss of existing livelihoods that cannot be replaced
after shrimp
farms are developed. Whilst it is often desirable to generate income in
coastal areas, this
has often been at the expense of the inhabitants of that area. The labour
requirement of
shrimp farms and processing plants is only useful if the demand is sustained.
To prevent
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 132
the boom–bust effect of shrimp farming, all people involved should aim
to maintain the
positive aspects of shrimp aquaculture whilst acting to ameliorate its
negative impacts.
When considering coastal areas for development, it is vital that existing
local
economies are evaluated correctly equitably and strong measures are taken
to avoid
explosive expansion of shrimp farms. It has been demonstrated frequently
that the ability
of a coastal area to support shrimp aquaculture is finite and that this
‘carrying capacity’
is often exceeded in the rush for quick profit. This approach, whilst
commonplace, is
ultimately to the detriment of all parties involved. click here to print
top
back
References
Avnimelech, Y., 1996. Shrimp pond bottom soils: Processes and management.
In: Book of Abstracts,
The 1996 Annual Meeting of the World Aquaculture Society, Bangkok, Thailand.
p. 24.
Bergheim, A., Kristiansen, R., Kelly, L., 1993. Treatment and utilization
of sludge from
landbased farms for salmon. In: Wang, J.K. Ed. , Techniques for Modern
Aquaculture.
Proceedings of an Aquacultural Engineering Conference, 21–23 June 1993.
Washington, DC, USA, 1134 pp.
Boyd, C.E., 1992. Shrimp pond bottom soil and sediment management. In:
Wyban, J. Ed. ,
Proceedings of the Special Session on Shrimp Farming. World Aquaculture
Society, Baton Rouge, LA, USA, pp. 166–181.
Briggs, M.R.P., Funge-Smith, S.J., 1994. A nutrient budget of some intensive
marine shrimp ponds in Thailand. Aquacult. Fisheries Manage. 25, 789–811.
Chanratchakool, P., Turnbull, J.F., Funge-Smith, S.J., Limsuwan, C., 1995.
Health Management in Shrimp Ponds—2nd edn.
Aquatic Animal Health Research Institute, Department of Fisheries, Bangkok,
Thailand, 111 pp.
Chong, K.-C., 1990. Structure, conduct and performance of the Asian shrimp
aquaculture industry.
In: New, M.B., de Saram, H., Singh, T. Eds. , Technical and Economic Aspects
of Shrimp Farming.
Proceedings of the Aquatec ’90 Conference Kuala Lumpur, Malaysia 11–14
June 1990, pp. 191–206.
Chua, T.E., Paw, T.N., Guarin, F.Y., 1989. The environmental impact of
aquaculture and the effects of pollution on coastal aquaculture development.
Asia Marine Pollution Bull. 20 7 , 335–343.
Csavas, I., 1993. Aquaculture development and environmental issues in
the developing countries of Asia. In: Pullin, R.S.V., Rosenthal, H., Maclean,
J.L. Eds. , Environment and Aquaculture in Developing Countries.
ICLARM Conference Proc. 31, 74–101.
Fast, A.W., Lannan, J.E., 1992. Pond dynamic processes. In: Fast, A.W.,
Lester, L.J. Eds. ,
Marine Shrimp Culture: Principles and Practices. Elsevier, Amsterdam,
pp. 431–456.
Flegel, T.W., Boonyaratpalin, S., Withyachumnamkul, B., 1996. Current
status of research on yellow-head virus and white spot virus in Thailand.
In: Book of Abstracts, The 1996 Annual Meeting of the World Aquaculture
Soc.
Bangkok, Thailand, p. 126.
Fry, J.C., 1987. Functional roles of the major groups of bacteria associated
with detritus. In: Moriarty, D.J.W., Pullin, R.S.V. Eds. , Detritus and
Microbial Ecology in Aquaculture, ICLARM Conference Proceedings 14. ICLARM,
Manila, Philippines, 420 pp.
Funge-Smith, S.J., 1996. Water and sediment quality in different intensive
shrimp culture systems in southern Thailand.
In: Coastal Aquaculture and Environment: Strategies for Sustainability.
ODA Research Project R6011, Institute of Aquaculture, University of Stirling,
Stirling, Scotland.
Funge-Smith, S.J., Stewart, J.A., 1996. Coastal Aquaculture: Identification
of Social,
Economic and Environmental Constraints to Sustainability with Reference
to Shrimp Culture.
In: Coastal Aquaculture and Environment: Strategies for Sustainability.
ODA Research Project R6011, Institute of Aquaculture, University of Stirling,
Stirling, Scotland.
Hopkins, J.S., Sandifer, P.A., Browdy, C.L., 1995. A review of water management
regimes which abate the environmental impacts of shrimp farming. In: Browdy,
C.L., Hopkins, J.S. Eds. , Swimming Through Troubled Water, Proceedings
of the Special Session on Shrimp Farming, Aquaculture ’95. World Aquaculture
Society, Baton Rouge, LA, USA.
( ) S.J. Funge-Smith, M.R.P. BriggsrAquaculture 164 1998 117–133 133
Liao, I.C., 1990. Aquaculture in Taiwan. In: Joseph, M.M. Ed. , Aquaculture
in Asia. Asian Fisheries Society,
Indian Branch, Mangalore, pp. 345–369.
Lin, C.K., 1989. Prawn culture in Taiwan. What went wrong?. World Aquaculture
20 2 , 19–20.
Macintosh, D.J., Phillips, M.J., 1992. Environmental issues in shrimp
farming. In: de Saram, H., Singh, T. Eds. , Proceedings of the 3rd Global
Conference on the Shrimp Industry, 14–16 September, Hong Kong.
INFOFISH, Kuala Lumpur, Malaysia, pp. 118–145.
Marsden, W., 1994. Modern Shrimp Farming—Sustainability and Environmental
Impact. Msc. Thesis, Institute of Aquaculture, University of Stirling,
Stirling, Scotland, 112 pp.
Masae, A., Rakkheaw, S., 1992. Social aspects of artisanal fisheries and
shrimp farming in Pak Phanang Bay.
Asian Fisheries Social Science Research Network: Coastal Resources Institute,
Prince of Songkhla University, Hat Yai, Thailand, 74 pp.
NACA, 1994. The environmental management of coastal aquaculture. An assessment
of shrimp culture in southern Thailand.
Final report to the Office of Environmental Policy and Planning. Network
of Aquaculture Centres in Asia-Pacific. January 1994.
Nuruzzaman, A.K.M., 1996. Socio-environmental impact of expansion of shrimp
culture: Lessons from Bangladesh. In: Proceedings of the 1996 Annual Meeting
of the World Aquaculture Society, Bangkok, Thailand. p. 287.
Panvisavas, S., Agamanon, P., Arthorn-Thurasook, T., Khatikarn, K., 1991.
Mangrove deforestation and land uses in Ban Don Bay, Thailand. ICLARM
22, 223–230.
Primavera, J.H., 1991. Intensive prawn farming in the Philippines: Ecological,
social, and economic implications. AMBIO 20 1 , 28–33.
Primavera, J.H., 1992. Prawnrshrimp culture in the Philippines. In: Fast,
A.W., Lester, L.J. Eds. ,
Marine Shrimp Culture: Principles and Practices. Elsevier, Amsterdam,
pp. 701–728.
Primavera, J.H., 1993. A critical review of shrimp pond culture in the
Philippines. Fish. Sci. 1 2 , 151–201.
Primavera, J.H., 1995. Mangroves and brackishwater pond culture in the
Philippines. Hydrobiologia 295, 303–309.
Rubel and Hager, 1979. Preliminary solids removal study. Rubel and Hager,
4400 E. Broadway, Tucson, AZ, USA.
Wang, J.K., Fast, A.W., 1992. Shrimp pond engineering considerations.
In: Fast, A.W., Lester, L.J. Eds. , Marine Shrimp Culture: Principles
and Practices. Elsevier, Amsterdam, pp. 415–429.
click here to print
or click here for the entire file 
top
back
|