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Accepted Manuscript Title: Waste treatment in recirculating aquaculture systems Author: Jaap van Rijn PII: S0144-8609(12)00094-5 DOI: doi:10.1016/j.aquaeng.2012.11.010 Reference: AQUE 1670 To appear in: Aquacultural Engineering Received date: 5-7-2012 Accepted date: 19-11-2012 Please cite this article as: van Rijn, J., Waste treatment in recirculating aquaculture systems, Aquacultural Engineering (2010), doi:10.1016/j.aquaeng.2012.11.010 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

Waste Treatment in Recirculating Aquaculture Systems

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Page 1: Waste Treatment in Recirculating Aquaculture Systems

Accepted Manuscript

Title: Waste treatment in recirculating aquaculture systems

Author: Jaap van Rijn

PII: S0144-8609(12)00094-5DOI: doi:10.1016/j.aquaeng.2012.11.010Reference: AQUE 1670

To appear in: Aquacultural Engineering

Received date: 5-7-2012Accepted date: 19-11-2012

Please cite this article as: van Rijn, J., Waste treatment in recirculating aquaculturesystems, Aquacultural Engineering (2010), doi:10.1016/j.aquaeng.2012.11.010

This is a PDF file of an unedited manuscript that has been accepted for publication.As a service to our customers we are providing this early version of the manuscript.The manuscript will undergo copyediting, typesetting, and review of the resulting proofbefore it is published in its final form. Please note that during the production processerrors may be discovered which could affect the content, and all legal disclaimers thatapply to the journal pertain.

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Waste treatment in indoor and outdoor RAS is reviewed

Little waste reduction takes place in indoor RAS

Outdoor RAS generally produce less waste than indoor RAS

Many on and off-site methods exist for waste reduction in freshwater RAS effluents

Treatment of effluents from marine RAS is little developed

*Highlights (for review)

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Waste treatment in recirculating aquaculture systems

Jaap van Rijn

The Robert H. Smith Faculty of Agriculture, Food and Environment

The Hebrew University of Jerusalem

P.O. Box 12, Rehovot 76100

Postal address: Department of Animal Sciences, The Robert H. Smith Faculty of

Agriculture, Food and Environment, The Hebrew University of Jerusalem, P.O. Box

12, Rehovot 76100, Israel. Phone: +972 8 9489302; Fax: +972 8 9489024; Email:

[email protected]

*Manuscript

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Abstract

Recirculating aquaculture systems (RAS) are operated as outdoor or indoor

systems. Due to the intensive mode of fish production in many of these systems,

waste treatment within the recirculating loop as well as in the effluents of these

systems is of primary concern. In outdoor RAS, such treatment is often achieved

within the recirculating loop. In these systems, extractive organisms, such as

phototrophic organisms and detritivores, are cultured in relatively large treatment

compartments whereby a considerable part of the waste produced by the primary

organisms is converted in biomass. In indoor systems, capture of solid waste and

conversion of ammonia to nitrate by nitrification are usually the main treatment steps

within the recirculating loop. Waste reduction (as opposed to capture and conversion)

is accomplished in some freshwater and marine indoor RAS by incorporation of

denitrification and sludge digestion. In many RAS, whether operated as indoor or

outdoor systems, effluent is treated before final discharge. Such effluent treatment

may comprise devices for sludge thickening, sludge digestion as well as those for

inorganic phosphate and nitrogen removal. Whereas waste disposed from freshwater

RAS may be treated in regional waste treatment facilities or may be used for

agricultural purposes in the form of fertilizer or compost, treatment options for waste

disposed from marine RAS are more limited. In the present review, estimations of

waste production as well as methods for waste reduction in the recirculating loop and

effluents of freshwater and marine RAS are presented. Emphasis is placed on those

processes leading to waste reduction rather than those used for waste capture and

conversion.

Keywords: recirculating aquaculture systems; RAS; waste treatment; waste

production; onsite treatment; waste disposal

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1. Introduction

Harmful effects attributed to aquaculture practices are of foremost concern to the

industry and are subject to increased public awareness (Sapkota et al., 2008;

Subasinghe et al., 2009). Often, these harmful effects are related to the environmental

impact of aquaculture activities, among those: (1) destruction of natural sites such as

wetlands and mangroves, (2) spread of diseases, (3) decreased biodiversity of natural

fish populations by escape of non-native fish species, and (4) pollution of ground and

surface waters by effluent discharge (Boyd, 2003).

Recirculating aquaculture systems (RAS), in which water is recirculated between

the culture and water treatment stages, provide an answer to some of the above

mentioned problems since they enable fish production in relative isolation from the

surrounding environment. However, this advantage is not without a price as many

challenges face the production of fish in these highly contained systems. In this

respect, water quality control and waste management are among the most critical of

these challenges. Careful design and management of RAS are the basis for a

successful waste management with respect to both waste production and treatment.

Operation of RAS under well controlled culture conditions contributes significantly to

an efficient feed utilization, hence, low waste production. Furthermore, proper

incorporation of treatment procedures within the recirculating loop or in the effluent

stream may further contribute to a significant reduction in waste production by these

systems. In most indoor RAS, the bulk of waste produced by the fish is captured and

removed in a concentrated effluent stream that may be treated onsite before final

discharge. Such onsite treatment generally involves sludge thickening and flow

stabilization but may also be designed to allow bacterial decomposition of solid waste.

Outdoor RAS, mostly situated in warmer climates, are often operated with partial

waste reduction within the recirculation loop. In the latter systems, phototrophic

organisms such as plants and algae are often involved in treatment of recirculation as

well as of effluent water.

This review summarizes some selected issues related to waste management in

RAS. Estimations of waste production are presented as well as methods for waste

reduction in the recirculating loop and effluents of freshwater and marine RAS.

Emphasis is placed on those processes leading to waste reduction rather than those

used for waste capture and conversion.

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2. Waste discharge regulation

Discharge regulations differ from country to country. Whereas in some jurisdictions

effluent standards are provided, in others, restrictions are placed on the amount of

feed or water that can be used by individual farms. However, the general tendency in

many countries is that, rather than effluent standards, guidelines for best management

practices or codes of conduct are provided together with measures to ensure

compliance to such guidelines (e.g. Environmental Protection Agency, 2004; Food

and Agricultural Organization, 1995). The rational of this approach is based on the

fact that universal guidelines as to effluent standards are difficult to formulate due to

differences in hydro-geographic, climatic and environmental conditions within

countries and regions. One such generic approach is the Life Cycle Assessment

(LCA). This method has received increased attention in recent years and has become a

recognized instrument in assessing the environmental impact of agricultural as well as

other production processes. Recently, it has also been applied for evaluating the

environmental impact of several aquaculture systems, including RAS (Martins et al.,

2010). Not only legislative bodies but also producer organizations advocate policies

for well monitored production regimes. Product quality, production transparency and

the added value of "environmentally friendly" raised products are major incentives for

promotion of these policies by such organizations (Boyd, 2003).

With respect to RAS, it is to be expected that operators of these, generally

well-managed systems are able to comply with compulsory monitoring and reporting

regimes. The high degree of fish confinement, the year-round production regime, the

use of monitoring systems, and the possibility for treatment of the concentrated waste

are all factors contributing to a transparency in reporting on the production process in

such systems.

3. Waste production

3.1 Feed conversion in RAS

Although liable to imprecision due to large differences in operational parameters, it

might be concluded that feed utilization by fish cultured in RAS often compares

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favorably to that of fish raised in other type of culture systems (Table 1). Production

of waste in RAS, like in any other aquaculture system, depends on a number of factors

with as most important ones: (a) the type and age of fish, (b) the feed composition, (c)

the feeding regime, and (d) the prevalent water quality conditions in the system. In

RAS, high feed utilization efficiencies can be attained by controlling some of these

factors. For instance, feeding in RAS, whether performed manually or automatically,

is well monitored. Hence, lapses of off-feed are easily identified thus minimizing

overfeeding and consequent accumulation of uneaten feed in the system. In addition,

batch-wise growth of uniform size classes of fish further contributes to an efficient

feed utilization in RAS (Karipoglou and Nathanailidis, 2009). Another factor

contributing to reduced feed wastage in RAS is water quality control. Treatment

systems in RAS are designed to control water temperature and critical water quality

parameters within an acceptable range hence avoiding inferior water quality

conditions and concomitant reduced feed utilization efficiency. Finally, in these

relatively well monitored systems, a quick response to changes in water quality

conditions may also contribute to an efficient feed utilization (Martins et al., 2010).

3.2 Quantifying of waste production

Waste production in aquaculture systems is quantified either by the nutritional

approach through determining the apparent feed digestibility of fish or is directly

analyzed by quantification of excretion products in the culture water (Cho et al.,

1991). Calculated values are often derived from feed trials under well-controlled

experimental conditions and not always reflect the feed digestibility of the fish under

more realistic culture conditions. In addition, due to partial breakdown of the waste to

gaseous forms within the culture system, not all of the generated fish waste is

discharged with the effluent water. Despite these shortcomings, the nutritional

approach is often preferred over the alternative method in which waste is directly

quantified in the culture system. Quantification of waste production by means of this

latter method, even in the simplest of experimental systems, is complicated due to the

difficulty in fitting a sampling regime to accurately estimate the fluctuating waste

production by fish. Furthermore, factors such as the cleaning regime of the culture

system, the frequency and duration of water replacement in the culture systems as

well as analytical errors in quantifying the waste products (e.g. sample preservation,

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analytical inaccuracies) contribute to the inaccuracy of the latter method (Roque

d'Orbcastel et al., 2008).

Organic matter, nitrogen and phosphorus utilization by the fish are main

indicators for the efficiency of feed utilization. Often these same parameters are also

used to quantify the environmental impact of aquaculture waste. Except for site

specific instances or in cases of highly concentrated effluents, other potential

environmental harmful ingredients of aquaculture waste, such as other inorganic

compounds, metals, drugs and pathogens, are monitored to a lesser extent. Clearly,

production of organic matter, nitrogen and phosphorus is directly linked to the food

conversion ratio and differs with different diets, temperatures, fish species, fish sizes

and culture systems (Table 2). By means of direct quantification, the partitioning of

nitrogen and phosphorus in solid and dissolved waste has been studied for most of the

commercially produced fish species (e.g. Azevedo et al., 2011; Lupatsch and Kissil,

1998; Piedrahita, 2003; Roque d‟Orbcastel et al., 2008). Despite the large variability

among fish species and culture methods, it can be concluded from these studies that,

in general, most of the nitrogen waste (60-90%) is in the dissolved form (mainly

ammonia) whereas for phosphorus, a larger proportion is excreted within the fecal

waste (25-85%).

In intensive production systems such as flow-through systems and cages,

waste production based on the nutritional approach (digestibility) might provide a

fairly accurate estimate for the waste that is discharged since in these systems most of

the fish waste is flushed out by water exchange. However, in RAS with a high degree

of recirculation, some of the waste is either passively or actively digested (Chen et al.,

1993; van Rijn et al., 2006) and waste production in these systems is lower than what

would be predicted by the nutritional approach. Due to differences in configurations

and management of RAS, losses of nitrogen and carbon within the system differ

widely among the different RAS (Chen et al., 1997; Piedrahita, 2003). A true

quantification of the waste production in these systems is therefore only possible by

direct measurements of waste in the effluent stream.

4. Onsite waste treatment

4.1. Reduction of waste within the RAS

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In most indoor RAS, ammonia removal and solids capture are the primary treatment

processes within the recirculation loop. Although intended to collect or convert fish

waste, these online treatment processes might lead to a considerable waste reduction

through production of mainly gaseous carbon and nitrogen compounds by biological

decay. The extent of this decay, mainly due to heterotrophic microorganisms, largely

depends on the specific system configuration. In particular, the water and solid

retention time of the system as well as methods used for water treatment within the

recirculating loop are major factors underlying such heterotrophic bacterial activity.

Sludge recoveries as low as 14% of the added feed, much lower than the calculated

sludge production (38-46%), were reported for recirculating systems not equipped

with dedicated treatment steps for sludge digestion (Chen et al., 1997; 1993). Also

Suzuki et al. (2003) found similar low sludge production values of 18% of the added

feed in a RAS not equipped with dedicated treatment for sludge removal. Not only

organic carbon but also nitrogen is lost from RAS. The loss of nitrogen is mainly due

to denitrification in oxygen depleted zones in the system and may account for as much

as 21% of the nitrogen loss in some RAS (reviewed by van Rijn et al., 2006).

Dedicated processes for waste reduction within the recirculating loop are

mainly found in outdoor, marine and freshwater RAS. Here, nutrients from the culture

water are removed by a combination of assimilatory and dissimilatory processes,

mediated by phototrophic and heterotrophic organisms. In this modern form of

polyculture, production of fed species (e.g. fish, shrimps) is integrated with that of

extractive species. In most of these so called integrated multi-trophic aquaculture

systems (IMTA), extractive species comprise phototrophic organisms such as plants,

microalgae and macroalgae but in some, also other organisms such as filter feeders,

detritivores and heterotrophic bacteria are produced. Examples of IMTA systems are

integrated marine systems (Neori et al., 2004 ), high rate algal ponds (Metaxa et al.,

2006; Pagand et al., 2000), aquaponic systems (Racocy, 2007), partitioned

aquaculture systems (Brune et al., 2003), active suspension ponds based on bio-flocs

technology (Avnimelech, 2003; Crab et al., 2007), periphyton systems (Schneider et

al., 2005; Verdegem et al., 2005), and constructed wetlands (Lin et al., 2005; Tilley et

al., 2002; Zachrits et al., 2008; Zhong et al., 2011). In many of these IMTA systems,

production of the primary aquatic species is combined with growth of other

economical valuable crops such as plants, filter feeding fish and detritivores (e.g.

clams and oysters). They provide, therefore, an elegant solution for increasing system

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productivity with concomitant reduction of waste output (Nobre et al., 2010).

Depending on the particular design and operating conditions, these IMTA systems are

operated without effluent discharge (e.g. partitioned aquaculture systems, active

suspension ponds), with discharge of solids (e.g. aquaponic systems, high rate algal

ponds), or, as common in marine systems, with solid and partial water discharge.

Most of above systems, in which treatment within the recirculation loop partially

depends on phototrophic organisms, are outdoor systems operated with relatively

large treatment areas under favorable climatic conditions. Hence, these latter systems

are more site-dependent than the more compact, indoor RAS systems.

Some indoor RAS, where ammonia is nitrified to nitrate, employ special

reactors to induce bacterial reduction of nitrate to nitrogen gas under anoxic

conditions. Most of these reactors are supplied with external carbon sources to fuel

heterotrophic denitrification. Others are designed to allow denitrification on internal

carbon sources which are produced in the RAS (van Rijn et al., 2006). In the latter

case, bacterial fermentation processes play an important role in supplying carbon

compounds for denitrification whereby most of the organic carbon is eventually

oxidized to CO2. Therefore, not only nitrogen but also organic carbon is removed by

means of this treatment combination (Eding et al., 2003; van Rijn et al., 1995). Eding

et al. (2009) calculated that by incorporating waste digestion and nitrate removal

within the recirculating stream, waste discharge for nitrogen and organic solids could

be reduced by 81% and 60%, respectively. An alternative treatment method based on

sludge digestion and bacterial nitrogen removal within the recirculation loop was

described by Tal et al. (2009). In this marine recirculating system, digestion of sludge

within a sludge digestion tank was allowed to proceed at low redox potentials to

produce sulfide which was subsequently used to fuel autotrophic denitrifiers in an

additional reactor. RAS incorporating sludge digestion and denitrification may be

operated with little to no effluent discharge as much of the waste is converted to

gases. They are, furthermore, operated with relatively small treatment volumes and

areas as compared to outdoor RAS (Table 3). Whereas in outdoor RAS, a

considerable part of the released phosphorus is assimilated by extractive organisms, in

indoor RAS, phosphorus is not removed within the system and is discharged in the

effluent stream. However, in systems incorporating sludge digestion and

denitrification within the recirculating loop, a considerable part of the dissolved

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orthophosphate was found to be immobilized during the latter treatment stages (see

next section).

Additional water treatment in the form of disinfection through ozonation and

UV irradiation of culture and discharge water are used in many indoor RAS operated

today (Goncalves and Gagnon, 2011; Summerfelt et al., 2009). Furthermore,

adsorption methods for removal of therapeutants have also been used in such systems

(Aitcheson et al., 2000). These compact, indoor systems potentially lend themselves

for use of recently developed water treatment technology such as electrochemical and

bio-electrochemical methods for removal of organic matter and inorganic nitrogen

(Mook et al., 2012; Virdis et al., 2008).

4.2 Onsite treatment of the effluent stream

4.2.1. Sludge thickening

Usually, RAS effluents are characterized by a low solid content (<2%) and fluctuate

in volume as a result of specific feeding and cleaning regimes. As direct disposal of

these effluents is costly, solids thickening and stabilization of the effluent flow is

often required before final disposal. Thickening of the sludge through settling of

solids in basins or ponds (Bergheim et al., 1993), through solids capture by means of

geotextile bags (Schwartz et al., 2005; 2004) or, more recently, by means of belt

filters (Timmons and Ebeling, 2007) and membrane reactors (Sharrer et al., 2007) are

applied in RAS. The various methods are often used in combination with

coagulation/flocculation processes to allow a more complete removal of suspended

solids as well as phosphorus from the effluent water (Danaher et al., 2011b; Ebeling et

al., 2006; Ebeling et al., 2003; Sharrer et al., 2009). In combination with dewatering,

the various methods used for sludge thickening may produce sludge with a solid

content of between 5 - 22% (Sharrer et al., 2009).

4.2.2. Sludge digestion

In addition to methods for sludge thickening, methods for enhancing biological

degradation of sludge are also used in treatment of RAS effluents. Waste stabilization

ponds such as aerobic and anaerobic lagoons might be used for this purpose as well as

sludge digesters (Chen et al., 1997). In the various ponds/reactors used for sludge

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digestion, sludge residence time (sludge age) is a major factor dictating the extent of

sludge degradation. Apart from the length of time during which the sludge is exposed

to microbial decay, the residence time also influences the type of electron acceptors

that are involved in sludge degradation. At relatively low retention times (e.g. settling

basins), oxygen will serve as the major electron acceptor while at higher retention

times (e.g. anaerobic lagoons), due to oxygen depletion, other electron acceptors such

as nitrate, sulfate (in marine systems) and carbon dioxide will be respired. Fast decay

of sludge in the presence of oxygen also coincides with fast growth in heterotrophic

biomass of the microorganisms involved in the sludge decay. Aerobic degradation

constants of "fresh" sludge were found to range from 0.07-0.40 day-1

(Boyd, 1973;

Chen et al., 1997). In settling basins operated at relatively long retention times, such

rapid breakdown of sludge and concomitant production of gases might cause poor

settling sludge properties (Timmons and Ebeling, 2007). In reactors operated at longer

retention times in which, besides oxygen, additional electron acceptors are respired,

decay of sludge proceeds at lower rates than under aerobic conditions and produces

less heterotrophic bacterial biomass. Sludge decay constants ranged from 0.024-0.006

day-1

in a reactor operated with a high sludge age with nitrate as the main electron

acceptor (van Rijn et al., 1995). Despite this apparently slow decay, this type of

reactor, when properly sized, can be operated for prolonged periods of time without

sludge wastage and, as discussed in the previous section, may be used as an on-line

treatment stage within the treatment loop. Sludge degradation of 30-40% was reported

for denitrifying reactors fed with marine RAS effluents and operated at shorter

retention times of up to 11 days (Klas et al., 2006).

Laboratory-scale sequencing batch reactors, operated under aerobic and anoxic

conditions, for removal of organic matter and nitrogen from concentrated sludge from

a shrimp facility were operated by Boopathy et al. (2007) and Fontenot et al. (2007).

They showed that at a hydraulic retention time of 8 days, a 74% reduction in organic

matter and a total reduction of nitrogen could be achieved with this kind a treatment

scheme.

Fully anaerobic, methanogenic digestion of aquaculture sludge has been

reported by several authors (reviewed by Mirzoyan et al., 2010). Although operational

conditions differ considerably among the few studies conducted, it can be concluded

that a considerable degradation and stabilization of aquaculture sludge can be

achieved through methanogenic digestion. Issues such as inhibition of the

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methanogenic activity by unionized ammonia concentrations due to low C/N ratios of

the sludge, optimal dry weight content of the sludge, and optimal hydraulic retention

times of the methanogenic reactors, still require further investigation prior to the full

scale use of these systems.

4.2.3. Inorganic nutrient transformations

Concentrations of inorganic nutrients in the supernatant of settlers and digesters are

dictated by the balance between chemical, physical and biological processes

responsible for their release from or removal by the sludge layer of the

settler/digester. Sludge residence time has a major influence on these processes. With

respect to nitrogen, ammonia concentrations are often found to increase due to

ammonification of nitrogenous organic matter (e.g. Conroy and Couturier, 2010;

Stewart, 2006). Various processes may counteract this ammonia accumulation.

Ammonia assimilation is particularly evident in reactors operated at high redox

potentials due to a relative large increase in bacterial biomass while nitrification of

ammonia may also take place in aerobic parts of the reactors (Cytryn et al., 2005; Klas

et al., 2006). Not only under aerobic conditions but also under anaerobic conditions

ammonia removal might take place. Under such conditions, nitrate, often present in

the RAS effluent stream, will not only be denitrified to elemental nitrogen at

appropriate hydraulic retention times, but may indirectly, through reduction to nitrite,

serve as an electron acceptor for anammox bacteria whereby both ammonia and nitrite

are converted to elemental nitrogen gas (Lahav et al., 2009; Tal et al., 2003).

In addition to ammonia release, hydrolysis of sludge in thickening reactors or

digesters leads to a release of orthophosphate. In their study on hydrolysis of

aquaculture sludge under static conditions, Conroy and Couturier (2010) showed that

orthophosphate release from the sludge was strongly correlated to the solubility of

calcium orthophosphates at low pH values. The same authors did not observed

orthophosphate release at pH values above 7.0. A decrease of orthophosphate in the

water column of reactors used for digestion of aquaculture sludge has been observed

in many studies (Barak and van Rijn, 2003; Barak et al., 2000a; Klas et al., 2006;

Neori et al., 2007; Sharrer et al., 2007; Tal et al., 2009). In addition to chemical

precipitation with mainly calcium and iron ions, biologically-mediated phosphate

sequestration may be of importance during digestion of aquaculture sludge. In nitrate-

rich digestion basins of freshwater and marine RAS it was found that denitrifiers

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accumulated orthophosphate as intracellular polyphosphate in excess of metabolic

requirements (Barak and van Rijn, 2003; 2000a). In these RAS, sludge from areas of

intensive denitrification was found to contain up to 19% phosphorus on a dry weight

basis while denitrifiers isolated from these systems were found to contain up to 9%

phosphorus on a dry cell weight basis (Barak and van Rijn, 2000b).

Release of reduced inorganic sulfur compounds during sludge

thickening/digestion may pose a potential problem with respect to effluent discharge.

This is especially true for marine RAS in which, under anaerobic conditions, sulfide

may be produced as a result of organic matter mineralization and sulfate reduction

(Cytryn et al., 2003; Schwermer et al., 2010; Sher et al., 2008). In these marine

systems it was found that the presence of nitrate during sludge digestion prevents

sulfide formation by exclusion of bacterial sulfate reduction (Schwermer et al., 2010)

as well as by promoting the growth of sulfide oxidizing, autotrophic denitrifiers (Sher

et al., 2008; Tal et al., 2009).

Depending on the accumulation of dissolved organic matter and nutrients in

sludge thickening reactors or sludge digesters, further onsite treatment of the

supernatant from these reactors may be warranted before final disposal. Brazil and

Summerfelt (2006) examined the effect of aerobic treatment of the supernatant

overflowing an aquaculture sludge thickening tank. They showed that in aerobic

reactors operated at hydraulic retention time of up to 6 days, an 87% reduction of

organic matter and total ammonia nitrogen and a 65% reduction in orthophosphate

could be achieved. In addition, outdoor treatment systems, similar to those used

within the recirculation loop (e.g. wetlands, high rate algal ponds) may also be used

for treatment of effluent water before final discharge or may serve both as an online

and effluent treatment stage. Largely depending on the size of such systems relative to

the waste load, these systems may be fed organic-rich water directly released from the

RAS or with supernatant from the sludge thickening stage (Cohen and Neori, 1991;

Metaxa et al., 2006; Neori et al., 1991; Pagand et al., 2000; Sindilariu et al., 2009).

5. Waste disposal

As apparent from the previous sections, the nature and quantity of waste disposed

from RAS depends largely on the onsite treatment facilities used. While several

alternatives are available for treatment of waste from freshwater RAS, waste

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treatment of waste from marine facilities is restricted to fewer methods. Liquid as well

as solid waste from freshwater RAS can be treated in centralized facilities such as

publicly owned treatment works (POWT) used for treatment of other livestock waste

as well as domestic and industrial waste. Where land availability and cost is less of a

constraint, these centralized facilities may be based on treatment by means of

stabilization ponds and wetlands. Alternatively, wastewater treatment facilities,

primarily used for treatment of domestic and industrial waste, with primary,

secondary and tertiary treatment steps, may also be used to treat RAS effluent.

However, treating aquaculture sludge in these latter systems seems wasteful as

concentrations of toxic and other health threatening components in aquaculture sludge

are low as compared to those in sludge from domestic and industrial origin. As such,

the use of aquaculture sludge as a fertilizer by direct land application (Bergheim et al.,

1993; Yeo et al., 2004) or its use for compost production (Adler and Sikora, 2004;

Danaher et al., 2011a) appear to be more sustainable alternatives. Composting might

require adjustment of the C/N ratio and a decrease of the water content of the sludge

by addition of a carbonaceous bulking agent in order to provide optimal aerobic

decomposition conditions (Adler and Sikora, 2004). Like the sludge also the liquid

fraction from RAS effluents may be used for irrigation of agricultural crops. Whereas

compost production is site independent, the use of solid as well as liquid waste for

fertilizer purposes depends on location. The absence of a properly scaled application

in the vicinity of the RAS, may prohibit this latter form of disposal (Yeo et al., 2004).

As most marine RAS are situated in close vicinity to the sea, waste discharge

into the sea is still the most common practice. While in marine RAS with online waste

treatment such practice results in little environmental impact such impacts may be

profound when waste is discharged from RAS with little post treatment. In the latter

case, the quantity of waste produced is not much different from cage aquaculture. In

coastal areas, constructed wetlands seem to be a promising method for treatment of

aquaculture waste (Gregory et al., 2010; Su et al., 2011). Where, due to site

restrictions, discharge to external facilities is not possible, on-site treatment systems

can be used by means of which excess nitrogen and carbon are converted into gases

(see section 4.1).

6. Conclusions

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Water treatment technology has seen a dynamic development in recent years

with new treatment methods rapidly emerging. Also in the field of RAS, a choice can

be made from many different treatment methods. The choice of a suitable treatment

method depends, in addition to a proper cost/benefit analyses, largely on factors,

directly or indirectly, related to the location of the recirculating system. Climatic

conditions, water availability, discharge regulations, and land availability are such

location-dependent factors which are major determinants for the type of treatment

methods to be used. These factors, together with the market value of the cultured

organisms, may justify the use of sophisticated treatment methods in some cases while

in others, optimal economical benefit is accomplished with relatively simple water

treatment techniques at the expense of water savings and production intensity.

In most outdoor RAS, waste reduction is generally achieved within the

recirculating loop by an integrative approach in which organic carbon and inorganic

nutrients are assimilated by phototrophic and heterotrophic organisms. Due to site and

climatic restrictions, indoor RAS are usually operated according to different treatment

protocols in which emphasis is placed on solid capture and ammonia transformation

to nitrate within the recirculation loop with optional onsite treatment of the

concentrated effluent before discharge.

It is expected that with increased fish demand as well as increased public

awareness related to issues such as overfishing, water savings, pollution, animal

welfare and ethics of animal husbandry, research on RAS as well as their commercial

exploitation will show a steady growth in the near future. The development of cost

efficient and sustainable waste treatment methods will be an important aspect

contributing to the wider use of these systems.

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Table 1. Feed conversion ratios in different types of culture systems

Species Flow

through

RAS Earthen

Pond

Cage Reference

Rainbow trout

(Oncorhynchus

mykiss)

0.8-1.2 0.8-1.1 - 1.1-1.3 Bureau et al. (2003);

Roque d'Orbcastel et al.,

(2009a,b,c)

Barramundi

(Lates

calcarifer)

-

-

0.8-1.1

1.5-2.2

1.6-2.0

FAO (2008); Peet (2006);

Schipp et al. (2007)

Tilapia

(Oreochromis

spp.)

- 1.0-2.2 0.8-3.5 >1.5 El Sayed (2006);

Leenhouwer et al., (2007);

Little et al. (2008); Martins

et al., (2009); Perschbacher

(2007); Schnell et al.

(2003)

Gilthead

seabream

(Sparus aurata)

- 0.9-1.9 - 1.4-2.2 Cromey and White (2004);

Zohar et al., (2005)

Cobia

(Rachycentron

canadum)

-

1.0

1.5

1.5-2.0

Benetti et al. (2008);

Kaiser and Holt (2005)

Table 1

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Table 2. Waste production of different fish species as determined by the nutritional approach

* numbers in parenthesis represent values that were obtained by direct quantification of the

waste in the culture water

Fish species Total solids Total N Total P Reference

(kg per ton fish production)

Rainbow trout

(Oncorhynchus

mykiss)

148-338 41-71 7.5-15.2 Azvedo et al. (2011); Bureau et

al. (2003); Roque d'Orbcastel

et al. (2008)

Brown trout*

(Salmo trutta)

438 (589) 49.2 (45.8) 6.2 (10.5) Cho et al. (1994)

Lake trout*

(Salvelinus

namaycush)

564 (562) 65.3 (59) 6.8 (6.8) Cho et al. (1994)

Barramundi

(Lates calcarifer)

29.0-302.3 21.8-101.7 4.2-15.4 Bermudes et al. (2010)

Gilthead

seabream

(Sparus aurata)

447.5 102.9 17.8 Lupatch and Kissil (1998)

Tilapia

(Oreochromis

spp.)

520-650 72.4 23-29 Beveridge (1984); Beveridge

and Phillips (1993)

Tilapia

(O. niloticus)

192-268.8 48-72.7 0.6-8.9 Schneider et al. (2004)

Atlantic salmon

(Salmo salar)

224 32 1.1 Reid (2007)

Table 2

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Table 3. Some characteristics of outdoor and indoor RAS with treatment components within the

recirculating loop

1 Treatment system was equipped with additional solids removal and nitrification units.

2 Treatment system was equipped with additional clarifier for solids removal.

3 Treatment system was equipped with additional nitrification unit.

Organism

cultured

Type of

treatment

Maximum

biomass

(kg)

Treatment volume and area Reference

Total Per kg of cultured

biomass

Outdoor RAS

Sea bass

(Dicentrachus

labrax)

High rate algal

pond1

320

14.0m3

26.0m2

0.044m3

0.081m2

Metaxa et al.

(2006)

Gilthead

seabream

(Sparus aurata)

High rate algal

pond1

520 12.0m3

43.7m2

0.023m3

0.084m2

Schuenhoff et

al. (2003)

Tilapia

(Oreochromis.

mossambicus x

O. aureus)

wetland2 1230 50.0 m

3

55.0 m2

0.041m3

0.045m2

Zachritz et al.

(2008)

Shrimps

(Litopenaeus

vannamei)

wetland2 924 21.0m

3

32.0m2

0.023m3

0.035m2

Lin et al.

(2005)

Tilapia

(O. niloticus)

aquaponics2

2184 80.0m3

232.0m2

0.037m3

0.106m2

Racocy et al.

(2004)

Indoor RAS

Tilapia

(O. niloticus x

O. aureus)

denitrification/

sludge digestion3

4800

40.0 m3

23.0 m2

0.008 m3

0.005 m2

Shnel et al.

(2002)

Gilthead

seabream

(Sparus aurata)

denitrification/

sludge digestion3

106 1.55m3

2.75m2

0.015 m3

0.026 m2

Gelfand et al.

(2003)

Gilthead

seabream

(Sparus aurata)

denitrification/

anammox/sludge

digestion3

1752 14.4m3

11.1m2

0.008 m3

0.006 m2

Tal et al.

(2009)

Table 3