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Aquaculture Research, 2016, 1–13 doi:10.1111/are.

12984

A comparison between water exchange and settling


tank as a method for suspended solids management
in intensive biofloc technology systems: effects on
shrimp (Litopenaeus vannamei) performance, water
quality and water use

Rafael Arantes1, Rodrigo Schveitzer2, Caio Magnotti1, Katt Regina Lapa1 & Luis Vinatea1
1
Department of Aquaculture, Federal University of Santa Catarina (UFSC), Laborat
orio de Camar~
oes Marinhos,
Florian
opolis, SC, Brazil
2
Department of Marine Sciences, Federal University of S~
ao Paulo (UNIFESP), Santos, S~
ao Paulo, Brazil

Correspondence: R Arantes, Department of Aquaculture, Federal University of Santa Catarina (UFSC), Laborat
orio de Camar~
oes
Marinhos, Florian
opolis, SC CEP 88062-601, Brazil. E-mail: arantesr75@gmail.com

ammonia. Both strategies are efficient in control-


Abstract
ling biofloc concentrations of the water; however,
Biofloc systems rely on microbial processes in the settlers can reduce water use and improve shrimp
water column to recycle animal waste products, production.
reducing the need for water exchange. These
increases biofloc concentration in the water and Keywords: biofloc, Litopenaeus vannamei, solids
some form of removal is needed. An experiment removal, water use
was carried out to evaluate two management
practices to control biofloc in Litopenaeus vannamei
Introduction
culture. Six tanks (48 m3) were divided into two
treatments: water exchange and solid settler. The use of biofloc technology (BFT) allows aqua-
Shrimp were stocked at 164 shrimp m2 and with culture managers to produce shrimp in densities
0.67 g of weight. After 61 days, shrimp under higher than 120 shrimp m2, with low or almost
solid settler treatment demonstrated mean weight no water exchange (WE) during the culture (Boyd
of 12.7  0.5 g with survival of 73.8  1.4%, & Clay 2002). This approach can improve biosecu-
and those under water exchange had a final rity and water conservation, expanding the possi-
weight of 10.1  0.2 g and survival rate of ble sites available for shrimp farming (Browdy &
57.8  11.1%. Total suspended solids did not dif- Moss 2005). The BFT system is based on high
fer between the treatments: 326.8  24.9 mg L1 rates of aeration and mixing (Browdy, Bratvold,
for water exchange and 310.9  25.3 mg L1 for Stokes & Mcintosh 2001). The management of a
solid settlers. Settleable solids and productivity/res- dense and active microbial community allows con-
piration ratio was higher (P < 0.05) in water trolling ammonia nitrogen concentrations in the
exchange treatment, indicating differences in phys- water without need for exchange (Avnimelech,
ical and biological characteristics of bioflocs. Solids Kochva & Diab 1994; Avnimelech & Kochba
removal method influenced the water use, in 2009). The microorganisms involved can form
which 1150  249 L of water was necessary to aggregates suspended in the water, known as bio-
produce one kilogram of shrimp using water flocs (De Schryver, Crab, Defoirdt, Boon & Ver-
exchange strategy, and 631  25 L kg1 with the straete 2008). In Biofloc tanks, ammonia can be
use of settlers. Our results indicate that continuous absorbed by microalgae and heterotrophic bacte-
operation of settlers can reduce variability in solids ria, or it can be transformed by nitrifying bacteria
characteristics and water quality variables such as (Ebeling, Timmons & Bisogni 2006).

© 2016 John Wiley & Sons Ltd 1


Two methods for solids management in BFT system R Arantes et al. Aquaculture Research, 2016, 1–13

The high feeding rates, usually applied to inten- (McIntosh 2000; Boyd & Clay 2002; Avnimelech
sive culture systems, contribute to the increase in 2009; Crab, Kochva, Verstraete & Avnimelech
total suspended solids (TSS), the variable used to 2009). In completely mixed shrimp tanks, turning
quantify bioflocs concentrations (Ebeling et al. off the central aeration equipment allows the set-
2006). A higher concentration of TSS may be tlement of bioflocs at the centre of the tank, and
related to poor water quality and may have nega- the sludge can be siphoned out or pumped from
tive effects on the health and performance of culti- the bottom (Hopkins 1994; Funge-Smith & Briggs
vated organisms (Hargreaves 2006; Van Wyk 1998; Taw 2012). The use of this method can
2006; Vinatea, G alvez, Browdy, Stokes, Venero, control solids concentrations without the costs of
Haveman, Lewis, Lawson, Shuler & Leffler 2010). installing removal devices. On the other hand,
In L. vannamei BFT culture system, TSS concentra- higher volumes of influent water can increase the
tion above 800 mg L1 was associated with lower risk of virulent pathogen infection (Lotz & Lightner
survival rates due to gill obstruction (Schveitzer, 1999) and promote water quality changes in tem-
Arantes, Costodio, Santo, Vinatea, Seiffert & perature or pH (Atwood et al. 2004; Crab et al.
Andreatta 2013). It was previously observed that 2009). Moreover, the effluent can adversely affect
removing a portion of TSS from culture water is water quality of adjacent environments (Jackson,
an important strategy for improving shrimp devel- Preston, Thompson & Burford 2003).
opment (Atwood, Bruce, Pierrard, Kelg, Stokes & Pilot-scale shrimp facilities were designed by
Browdy 2004; Van Wyk 2006; Ray, Shuler, Leffler using settling chambers to remove solids (Ogle,
& Browdy 2009). In shrimp culture with biofloc, it Flosenzier & Lotz 2006). Settling is an effective
has been suggested that TSS should be maintained technology that costs less than filtration and flota-
between 400 and 600 mg L1 (Ray, Lewis, tion (Timmons & Ebeling 2007), and could be
Browdy & Leffler 2010; Vinatea et al. 2010; used in large-scale operations. Although settling
Schveitzer, Arantes, Baloi, Costodio, Arana, Seiffert and WE have been used in shrimp production, the
& Andreatta 2013; Schveitzer, Arantes, Costodio efficiency of these two management strategies
et al. 2013). To assess similar benefits, it is also needs to be addressed. The purpose of this study
possible to maintain the volume of settleable solids was to compare these two methods for suspended
(SS) between 10 and 15 mL L1 (Taw 2012). solids management in intensive BFT systems.
Different strategies have been used to reduce
bioflocs levels in BFT culture systems: sand filters
Material and methods
(Samocha, Patnaik, Speed, Ali, Burger, Almeida,
Ayub, Harisanto, Horowitz & Brock 2007), bead
Shrimp source
filters (Atwood et al. 2004), foam fractionators
(Otoshi, Tang, Dagdagan, Holl, Tallamy, Moss, The study was carried out at the Laborat orio de
Arce & Moss 2006; Mishra, Samocha, Patnaik, Camar~ oes Marinhos (LCM), in Santa Catarina, Bra-
Speed, Gandy & Ali 2008) or settling tanks (Rak- zil. Ten-day-old post-larvae (PL10) of Litopenaeus
ocy 2002; Ray, Lewis et al. 2010; Ray, Dillon & vannamei were obtained from a commercial hatch-
Lotz 2011). In general, the completely mixed ery (Aquatec LTDA, in Brazil), and cultured at a
water is collected, passed through a solids-removal nursery in an 8-meter-diameter round tank filled
device and flows to the culture tank with lower with 43 m3of filtered sea water.
solids concentration (Rakocy 2002). This process The nursery tank was inoculated with 5 m3 of
reduces mean biofloc residence time in the culture a mix of two diatoms cultures (Thalassiosira weiss-
tanks, removes refractory solids and could reduce flogii and Chaetoceros muelleri), at a density of
the amount of water used for rearing (Ebeling ~3 9 104 cells mL1 each, to help maintain water
et al. 2006; Schveitzer, Arantes, Baloi et al. 2013; quality until a heterotrophic community was
Schveitzer, Arantes, Cost odio et al. 2013). Addi- established. Dried molasses with 42% carbon or
tionally, the use of these devices could help to sta- 69% of carbohydrate content was added daily.
bilize the composition of the microorganism Additions were divided between feed input to
associated with the bioflocs (Hargreaves 2006; maintain a carbon to nitrogen (C:N) ratio above
Ray et al. 2009). 12:1 and control ammonia-nitrogen build-up
Large-scale systems normally rely on some (Avnimelech 1999). The tank was stocked at a
WE to remove solids and to improve production density of 1100 PLs m2. The shrimp were fed a

2 © 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13


Aquaculture Research, 2016, 1–13 Two methods for solids management in BFT system R Arantes et al.

40% protein commercial diet (Guabi, LTDA) four In the WE treatment, the central aeration ring
times a day according to a feed chart (Van Wyk valve was closed for 15 min to allow the solids to
1999). The shrimp were cultured for 31 days, and settle at the centre of the tank. Bottom water rich
then gradually acclimated from 34 to 16 g L1 in solids was then flushed out through the central
salinity according to Roy, Davis, Saoud, Boyd, Pine drain line linked to a stand pipe. The volume of
and Boyd (2010) using tap water filtered at water removed from each tank varied within a
25 lm. After 3 days at salinity of 16 g L1, all range of 1026–5000 L at each draining event.
the shrimp were harvested and stocked in the The time to stop the drainage was calculated by
experimental tanks. using the SS volume measured into the drain
water, the drain line water flow, and the amount
of solids needed to be reduced from the tanks. This
Experimental design
was used to trying to reach a TSS value in culture
The units consisted of six 50 m3 circular fibreglass water between 400 and 600 mg L1 (Ray, Lewis
tanks (water volume of 48 m3). A central aeration et al. 2010; Vinatea et al. 2010; Schveitzer, Aran-
ring with 50 cm in diameter made of PVC pipe tes, Baloi et al. 2013; Schveitzer, Arantes, Cost
odio
(32 mm) perforated with 0.75-mm holes was pro- et al. 2013). The volume of water removed from
vided to maintain the solids in suspension and to each tank (Vdrain) was calculated using the follow-
increase dissolved oxygen levels. Another circular ing equation:
PVC pipe placed at the periphery of the tank was
Vdrain ¼ ðSStq  VolumeÞ  ðSSFinal
equipped with 15 air-lift pumps (100 mm in diam-
 VolumeÞ=SSeffluent ð1Þ
eter) to provide water aeration and movement in a
circular pattern. A 7.4-HP regenerative blower
was used to aerate all six tanks. Finally, all tanks where: Volume = total volume of culture tank (L);
were individually covered with a transparent PVC SStq = SS present in culture tank (mL L1); SSfinal
liner and with a 70% shade cloth to reduce light = SS desired in culture tank (mL L1); SSeffluent =
intensity. SS in the drainage water (mL L1).
Two treatments were used to evaluate the effects In the treatment with settlers (SE), the TSS con-
of the suspended solids reduction strategies. In one centration was maintained by using one 1.2 m
treatment, solids concentration was managed by diameter (0.8 m3) cylindro-conical settler per tank.
settling in the tank and subsequent WE, in the The settling chambers were adapted from Ray,
other treatment settling chambers were used to Lewis et al. (2010) and Davidson and Summerfelt
reduce solids concentration (SE). Each treatment (2005) and were continuously operated to main-
was randomly assigned to three replicate tanks. In tain TSS concentration close to 400–600 mg L1.
a different tank, the same procedure was applied The flow rate of the settlers (FRs) was calculated
to prepare water used to exchange or replace the according to the daily feeding input as described in
culture tanks. Before stocking, tanks received Eqn (2), considering a TSS production between
3 m3 of water each from the nursery tank as ino- 0.36–0.65 of the total feed applied daily to the
colum, and stocked with juvenile pacific white tanks (Ebeling et al. 2006).
shrimp with an initial weight of 0.67  0.1 g for
a stocking density of 164 m2. The experiment FRs ¼ ½ðRfeed  TSSP Þ  ER1 1
%   TSStank ð2Þ
was ended when shrimp in the fast growth treat-
ment reached the average commercial size of 12 g where: FRs = flow rate of settler (m3 day1); Rfeed
(Tahim & Araujo 2012). = feed applied to culture tank (g day1); TSSp =
TSS produced per gram of feed applied to culture
tank (g g1); ER% = TSS removal efficiency;
System management
TSStank = concentration of TSS into tank water
The volume of SS was monitored daily, using a (g m3).
15-min settling time (APHA 1998– 2540F, The flow rate of settling tanks was monitored
adapted by Avnimelech 2007). When the volume twice a day using a stop watch and a beaker and
reached 15 mL L1, a periodic removal was initi- was adjusted daily to prevent sudden changes in TSS
ated by using two different treatments trying to concentrations based on the SS volume from one
maintain SS values under this limit. day to another. Total suspended solids (TSS) from

© 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13 3


Two methods for solids management in BFT system R Arantes et al. Aquaculture Research, 2016, 1–13

the tank water and from water flowing back into the defined as the volume occupied by each gram of
culture were sampled twice a week to monitor TSS TSS in the water and was calculated according to
ranges and to access the TSS removal efficiency of Eqn (3) (Gray 1990).
the settlers (Davidson & Summerfelt 2005).
Water temperature of the entire system was
SVI ¼ SS  ðTSS  1000Þ1 ð3Þ
controlled using one 5 kW eletrical water heater
operated at night. To prevent a drop in alkalinity
where: SVI = Sludge volume index (mL g1); SS =
below 120 mg L1, hydrated lime was applied at
setteable solids (mL L1); TSS = total suspended
the rate of 12% of daily feed input. For each tank,
solids (mg L1).
a mixture containing 35% rice bran (C:N = 20:1)
and 65% dried molasses (C:N = 76:1) was used in
addition to the feed (C:N = 7:1) to increase the Microbial activity
total carbon to nitrogen ratio to 12:1. The organic
Microbial activity in the water was monitored
fertilizer was applied to the tanks three times a
weekly according to the methodologies proposed
day, 1.5 h after feeding to prevent a drop in dis-
by Bratvold and Browdy (1998) and Vinatea et al.
solved oxygen (DO). All the materials used as a
(2010). The term microbial activity used in this
fertilizer were analysed (Labcal-UFSC). Whenever
study was proposed by Bratvold and Browdy
TAN concentrations exceeded 1 mg L1, an addi-
(1998) and involves two microbial processes: gross
tional dried molasses input were applied using
primary production (P) and water column respira-
20 g of carbohydrates per gram of total ammonia
tion rate (R). Both were measured using the light–
nitrogen (TAN) needed to be reduced (Avnimelech
dark bottles method (Strickland 1960), and the
1999). This methodology was used in order to
calculations were performed according to Dodds
momentarily increase C:N ratio and avoid concen-
and Cole (2007):
trations higher than 1 mg L1. When needed, the
additional molasses input was divided at least in P ¼ ðfinal O2 light bottle
six applications, or two consecutive days, in order  final O2 dark bottleÞ  time1 ð4Þ
to avoid low DO levels. The shrimp were fed three
times per day with 35% crude protein (CP) com- where: P = gross primary production (mg
mercial diet (Guabi LTDA). Three feeding trays O2 L1 h1)
received 15% of the feed applied to each tank, and
were used to check the amount of feed consumed R ¼ ðinitial O2 of dark bottle
after 1.5 h to avoid overfeeding (Casillas-Hernan-  final O2 dark bottleÞ  time1 ð5Þ
dez, Magall~aes-Barajas, Portillo-Clarck & Paez-
where: R = water column respiration rate (mg
Osuna 2006).
O2 L1 h1)
The analyses were performed by incubating
Water quality monitoring
the transparent (primary production) and dark
Dissolved oxygen and water temperature (YSI (respiration) DBO bottles (300 mL) immersed at a
550A, Yellow Springs, HO, USA) were measured depth of 10 cm in the tank water. All bottles
twice a day, the salinity (YSI 30 salinity meter) was were incubated in duplicate for 90 min. The con-
measured daily, and the pH (YSI model100 pHme- sumption (respiration) and production (photosyn-
ter) was analysed twice a week. The alkalinity of thesis) of oxygen in the water column were
water based on CaCO3 (APHA 1998 – 2320 B), the estimated by measuring the variation in DO in
TSS (APHA, 1998 – 2540D) using 0.6 lm fibre- the bottles with a water sample from the tanks.
glass microfilters (GF-6 Macherey-Nagel, Bethle- To keep the flocs in suspension inside the bottles
hem, PA, USA) were analysed weekly. Ammonium during the incubation, the bottles were manually
(TAN) (Koroleff 1969), nitrite (Bendschneider & agitated every 20 min for about 3 s (Schveitzer,
Robison 1952), nitrate (HACH – 8039 cadmium Arantes, Baloi et al. 2013; Schveitzer, Arantes,
reduction HACH, Loveland, CO, USA) were analysed Costodio et al. 2013). The initial and final oxy-
weekly with a LaMotte Smartspectro spectrometer. gen concentration was measured with a YSI
The sludge volume index (SVI) is a ratio between 5100 oximeter using a specific probe with self-
the SS volume and the TSS concentrations. It is agitation.

4 © 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13


Aquaculture Research, 2016, 1–13 Two methods for solids management in BFT system R Arantes et al.

America, Brazil) and the results were presented as


Water use
means  SD.
The total amount of water used per tank was cal-
culated by the sum of the sludge volume produced
Results
during the culture period and the total water dis-
charged from the tanks after harvest. Solids
Control of suspended solids concentration
retained in the settling chambers were drained
from the base of the cone four times during the The concentration of TSS increased in both treat-
rearing period. The sludge volume was determined ments until the fourth week of the experiment,
using a graduated 40-L bucket. The effluent vol- reaching 465.0  95.0 mg L1 in the WE treat-
ume from the WE treatment was recorded directly ment and 429.3  6.4 mg L1 in the SE treat-
from the volume reduction of the tanks after water ment (Fig. 1). After the initiation of solids
removal, just before water was refilled in the removal in the fourth week, TSS concentrations
tanks. Aliquots of the sludge and the effluent were remained between 400 and 500 mg L1 and
taken to determine TSS concentration in the WE were not significantly different until the end of
and SE treatments respectively. The total amount the study (Table 1). Flow rates applied to settlers
of solids discharged was calculated using the vol- ranged from 115.4 to 185.6 L h1, and the
ume of sludge or volume of final effluent water dis- solids removal efficiency ranged between 57%
charged and their respective TSS concentration. and 65%.
Water addition to all units was needed to replace Until the sixth week, the SS were similar in
evaporative losses and sludge removal. both WE (10.0  2.0 mL L1) and SE
(9.3  3.2 mL L1) treatments. In the seventh
week, SS was higher in the WE treatment, and
Shrimp monitoring
until the end of the experiment, it remained higher
Weight gain was monitored weekly by weighing than in SE (Fig. 1). In WE, the SVI values were
three groups of at least 80 shrimp per tank using superior (23.0  2.82 mL g1) than in the SE
a digital scale. The final weight (g), survival (%), treatment (16.7  2.19 mL g1) during the last
growth rate (g per week) and final biomass 3 weeks of the rearing period (Fig. 1).
(kg m3) were recorded at the end of the experi-
ment and used to assess the culture performance.
Water quality
The feed conversion ratio (FCR) was estimated as
the total dry weight of the feed supplied/shrimp Water temperature (28.4  0.9°C), dissolved oxy-
wet weight gain. gen (5.3  0.5 mg L1), pH (7.7  0.0) and
salinity (16.2  0.3 g L1) were similar in both
treatments. Minimum dissolved oxygen of 3.7 and
Statistical analisys
3.9 mg L1 and maximum of 7.4 and 7.1 mg L1
Culture performance data and effluent volume were recorded for treatments WE and SE respec-
were analysed using one-way ANOVA. Mean weight tively. The average C:N ratio for both treatments,
(g), feed intake (kg per week) and water quality calculated from the amount of feed, molasses and
data were compared using one-way ANOVA with rice bran, was 12.1  0.1.
repeated measures. Treatments were considered Total ammonia nitrogen and nitrate concen-
the main factor and the culture weeks, the addi- trations were also similar in both treatments
tional factor (Gomez & Gomez 1984). Significant (Table 1). In SE, TAN concentration was vari-
differences were analysed using Tukey’s test at a able in the fourth week (1.2  0.8 mg L1) and
5% significance level. Normality and homoscedas- remained close to minimum detection limits of
ticity were tested using Shapiro–Wilk (Zar 1999) the method in the following weeks. In WE, the
and Bartlett (Gomez & Gomez 1984) tests variation in TAN initiated at week 5
respectively. Percentage data were analysed using (1.3  1.7 mg L1) and reached a maximum
data transformed into arc-sine (y0.5); variables value of 4.3 mg L1 at week 7 (Fig. 2). In both
without homogeneous variances were transformed treatments, nitrate concentrations increased
to log (x + 1). Statistical analyses were conducted after the fifth week. By the harvest time, mean
using the STATISTICA Version 8 (StatSoft South nitrate concentration was not significantly

© 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13 5


Two methods for solids management in BFT system R Arantes et al. Aquaculture Research, 2016, 1–13

Figure 1 Total suspended solids


(TSS) (a), settleable solids (SS) (b)
and sludge volume index (SVI) (c)
during nine culture weeks of
Litopenaeus vannamei with two
methods of solids control: water
exchange (WE) and use of solids
settler (SE). Asterisks indicate sta-
tistically significant differences
between treatments (P < 0.05).

different between the treatments (P > 0.05), decreased from the second to the fifth weeks of the
48.5  2.1 mg L1 for WE and 32.3  14. culture and reached values below 1 (Fig. 3). After
4 mg L1 for the settlers treatment (Fig. 2). periods of solids removal in both treatments, P/R
Nitrite was significantly higher in the SE treat- ratio increased again to values >1 indicating pre-
ment (Table 1), and in both treatments, nitrite dominance of photoautotrophic microorganisms.
concentrations increased significantly after week Water exchangeshowed a higher P/R ratio when
4 (Fig. 2). compared to SE (P < 0.05; Fig. 3).

Microbial activity Shrimp production

Respiration rates of the microbial community All shrimp production parameters differed signifi-
suspended in the water of WE (0.8  0.0 cantly in the treatments (Table 2), except for sur-
mg L1 h1) did not significantly differ from the vival (P = 0.06). Shrimp from the SE treatment
SE (0.9  0.0 mg L1 h1) (Table 1; Fig. 3). The showed significantly lower FCR and the final
ratio of gross primary production to respiration biomass of shrimp was 60% higher compared to
(P/R) were not measured in the first week, but the WE; demonstrating a higher weekly weight

6 © 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13


Aquaculture Research, 2016, 1–13 Two methods for solids management in BFT system R Arantes et al.

Table 1 Water quality variables and microbial activity parameters in tanks of Litopenaeus vannamei cultured with two
methods of solids removal: WE and use of SE

Treatment† ANOVA‡

Variables WE SE (T) (W) (T 3 W)

1
TSS (mg L ) 326.8  24.9 (102.0–575.0) 310.0  17.5 (95.5–499.0) NS * NS
SS (mL L1) 9.38  0.7 (0.0–21.0) 6.14  1.0 (0.0–14.0) * * *
TA-N (mg L1) 0.48  0.2 (0.0–4.6) 0.36  0.0 (0.0–2.5) NS NS NS
Nitrite-N (mg L1) 0.31  0.1b (0.0–0.9) 0.46  0.0a (0.0–1.0) * * NS
Nitrate-N (mg L1) 15.3  2.1 (0.0–50.8) 12.8  3,5 (0.0–46.3) NS * NS
Respiration (R) (mg L1 h1) 0.8  0.0 (0.5–1.2) 0.8  0.04 (0.3–1.4) NS NS NS
Production/Respiration 1.6  0.2a (0.3–4.5) 1.0  0.1b (-0.3–2.0) * * NS

†Values are mean  SD (range); a,b(P < 0.05).


‡ANOVA with repeated measures, T (treatment), W (Week), T 9 W (Interaction T 9 W); *(P < 0.05).
NS, not significant; TSS, total suspended solids; SS, settleable solids; TA-N, total ammonia nitrogen; WE, water exchange; SE, solids
settling.

Figure 2 Total ammonia nitrogen


TAN (a), nitrite NO2-N (b), nitrate
NO3-N (c) duringnine culture
weeksof Litopenaeus vannamei with
two methods of solids control:
water exchange (WE) and use of
solid settler (SE). Asterisks indicate
statistically significant differences
between treatments (P < 0.05).

© 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13 7


Two methods for solids management in BFT system R Arantes et al. Aquaculture Research, 2016, 1–13

Figure 3 Water column respira-


tion rates (R) (a), Production to
respiration ratio (P/R) (b) during
nine culture weeks of Litopenaeus
vannamei with water exchange
(WE) and use of settler (SE). Aster-
isks indicate statistically significant
differences between treatments
(P < 0.05).

Table 2 Shrimp production in tanks with Litopenaeus observed in the SE treatment (Table 3). Consider-
vannamei cultured with two solids removal methodolo- ing the total water used, only 2.5% was used
gies: WE and use of SE. Initial stocking density 164 during culture to replace from sludge removal in
shrimp m2, 61 days of culture with an initial weight of the SE treatment, compared with the 14% of that
0.64 g water removed by tank draining in the WE.
Higher solids concentrations (13 times greater)
Treatment*,†
were found in the effluent generated from the SE
Parameter WE SE treatment (33.4  6.2 g L1), which differ
(P < 0.05) from those in the WE treatment
Final average weight (g) 10.1  0.2a 12.7  0.4b
(2.5  1.4 g L1). The amount of feed applied to
Average weekly growth (g) 1.1  0.0a 1.4  0.1b
Survival (%) 57.8  11.0 73.8  1.4 the tanks along culture was 99.0  6.7 kg for SE
FCR 1.9  0.3a 1.3  0,0b and 81.7  4.5 kg for WE. The total amount of
Final Biomass (kg m3) 1.0  0.2a 1.6  0.0b solids removed on final effluent and as sludge
during culture are described in Table 3. Solids
*Values are mean  SD.
†Different letters indicate significant difference by Tukey’s test on sludge removed from WE treatment
(P < 0.05). (38.0  0.8 kg) were higher than that removed
WE, water exchange; SE, solids settling. from SE (19.4  9.4 kg).

gain (Table 2). Significant differences were found


Discussion
in the mean weight of shrimp from week 6, and at
the end of the experiment, the average shrimp
Control of suspended solids concentration
weight was 2.6 grams higher in SE (P < 0.05).
The TSS concentration was relatively stable
throughout the final 6 weeks of the culture per-
Water use
iod, indicating the effectiveness of the solids
The WE treatment consumed a higher amount of control methods tested. In both treatments, the
water during culture (P < 0.05) than that amount of solids removed from final effluents were

8 © 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13


Aquaculture Research, 2016, 1–13 Two methods for solids management in BFT system R Arantes et al.

Table 3 Use of water per culture tank, water use effi- monitoring of biofloc concentration through the SS
ciency per kilogram of shrimp produced and solids measurement in this treatment, leading to difficul-
removed for treatments with WE and with the use of SE ties to TSS control. The problems in tracking TSS
concentration by biofloc volume measurements
Treatment*,†
(SS) has been reported by Ray et al. (2011). In SE
Parameter WE SE treatment, the continuous operation of settling
tank kept the values of SS stable, however, the use
Total water used 53 920.0  1143.1a 48 565.0  347.2b
of this variable to indicate the concentration of TSS
(L per tank)
Water used during 7643.3  3691.7a 1185.0  13.6b needs caution (Schveitzer, Arantes, Baloi et al.
culture (L per tank) 2013; Schveitzer, Arantes, Cost odio et al. 2013).
Water use 1150.8  249.1a 631.9  25.1b
efficiency (L kg1)
Solids on final 19.3  0.1a 15.7  0.1a Microbial activity
effluent (kg)
Solids on sludge 38.4  0.8a 19.4  9.4b The calculation of SVI can be useful as a tool for
removed (kg) indicating changes in physical features of the bio-
flocs. The changes in SVI values are normally
*Values are mean  SD.
linked to shifts in the characteristics of the biofloc
†Different letters indicate significant difference by Tukey‘s test
(P < 0.05). microbial community (Graddy, Daigger & Lim
WE, water exchange; SE, solids settling. 1999). Higher SVI values, above 60 mL g1, are
usually found in bioflocs with high abundance of
filamentous forms of bacteria and cyanobacteria,
similar, even with a higher quantity of TSS since the amount of free space within the flocs
removed from sludge during culture in the WE increases (Graddy et al. 1999; De Schryver et al.
treatment. In this treatment, a higher P/R ratio 2008). In the WE treatment, the higher SVI sug-
(higher predominance of photoautotrophic gests that changes in the microbial community
microorganisms) can be associated with a higher may be associated with the solids removal process.
TSS production (Ebeling et al. 2006). Solids This is also supported by the differences in microbial
production within biofloc culture may be variable, P/R ratio, observed after the start of WEs, indicating
primarily due to its association with the predomi- greater photoautrotrophic activity (Burford,
nant pathway for ammonia control by the micro- Thompson, McIntosh, Bauman & Pearson 2003).
bial community (Ebeling et al. 2006). Considering In the first 5 weeks of culture, the decrease in
the difficulty in controlling the roles of these meta- the P/R ratio was inversely associated with TSS,
bolic pathways in the culture, it is necessary to as respiration rates did not significantly change
monitor constantly the amount of solids in the during this period. Lower primary production rates
water to control their concentration properly were reported to be related to an increase in solids
(Avnimelech 2009). concentration (Vinatea et al. 2010). According to
One way to facilitate solids control is to estimate these authors, an increase in photoautotrophic
their production due to the feeding input (Chen, activity was observed after the start of the solids
Coffin & Malone 1997; Ebeling et al. 2006). Values removal process, as also found by this study. The
for flow rate and TSS removal efficiency of the causes of the increased P/R ratio in the WE treat-
settling tanks suggest that in SE treatment, the ment are unclear, the removal of microbial bio-
adjustment of the flow rate could be regulated by mass combined with clear water additions may
the input of feed into the tanks on the day before have increased light availability, favouring the
and it allowed an approximate control of the solids. dominance of photoautotrophic microorganisms
In the WE treatment, the solids control was also (Weirich, Browdy, Bratvold, Mcabee & Stokes
associated with the feed input, however, care has 2002; Vinatea et al. 2010).
to be performed to prevent either insufficient or For the SE treatment, unchanged conditions of
excessive removal of water and solids. Abrupt the solids characteristics are indicated by the con-
changes possibly lead to variations in biofloc physi- stant SVI values. This pattern may be related to
cal characteristics (Martins, Heijnen & Van Loos- the continuous operation of the settling chambers.
drecht 2003). In WE, the increase in the SS volume Settling tanks allowed the removal of particulate
without any change in TSS profile changed the material slowly and without sudden changes.

© 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13 9


Two methods for solids management in BFT system R Arantes et al. Aquaculture Research, 2016, 1–13

According to Ray et al. (2009) and Ray, Seaborn, between the fifth week (maximum value of
Leffler, Wilde, Lawson and Browdy (2010), con- 3.2 mg L1) and the seventh week (maximum
stant solids removal is the most effective tool for value of 4.6 mg L1) displayed values above the
encouraging the stability of the microbial commu- safe concentration of 2.4 mg L1 for L. vannamei
nity and for improving productivity of the target juveniles reared at salinity of 15 g L1 (Lin &
species. Chen 2001), exposing the animals to adverse con-
ditions that can affect their growth (Hargreaves
1998; Avnimelech 2009). In addition, changes in
Water quality
SVI and P/R ratio suggest changes in physical and
Temperature, pH, dissolved oxygen, salinity and biological characteristics of bioflocs (Graddy et al.
alkalinity were within appropriate values for the 1999; Burford et al. 2003; De Schryver et al.
intensive cultivation of L. vannamei (Van Wyk & 2008) and could be associated with the reduced
Scarpa 1999; Roy et al. 2010). shrimp growth and lower final biomass in this
Changes in ammonia concentration between the treatment (Ray et al. 2009; Furtado, Poersch &
fourth and the fifth week and the increasing values Wasielesky 2011).
of nitrite and nitrate in the following weeks may Shrimp production in the SE treatment resulted
indicate the start of nitrifying bacteria activity in higher final weight and higher biomass. We
(Cohen, Samocha, Fox, Gandy & Lawrence 2005; suggest that these values are associated with the
Mishra et al. 2008). In the SE treatment, ammonia stability of ammonia levels and to the quality of
values approached the minimum limits of detection solids, provided by the use of settling chambers. As
(0.007 mg L1) during week 5, suggesting the described in previous studies, the continuous
presence of sufficient nitrifying biomass to control removal of a portion of bioflocs may have con-
ammonia production. In the WE, the removal of tributed to the development of a healthier and
solids in the fourth week may have led to a delay more stable microbial community, providing bene-
in the oxidation of ammonia to nitrite, as indicated fits to the cultured animals (Turker, Eversole &
by the increased TAN variability, and to the lower Brune 2003; Atwood et al. 2004; Ray, Lewis et al.
nitrite values found in this treatment (Cromar & 2010; Ray, Seaborn et al. 2010).
Fallowfield 1997; Ebeling et al. 2006). The same
variability of ammonia and nitrite due to solids
Water use
removal has been reported by Ray et al. (2011).
The effectiveness of water conservation in shrimp
culture can be measured by the amount of water
Shrimp performance
used to produce 1 kg of shrimp (Browdy & Moss
The shrimp growth and the FCR found in this 2005). The value of 1150 L kg1 for WE treat-
study were similar to those found in other studies ment was lower than those reported from inten-
(Ray et al. 2011; Schveitzer, Arantes, Baloi et al. sive biofloc cultivation in ponds where they were
2013). Growth rates between 1.3 and 1.7 g per 2000–2260 L kg1 (McIntosh 1999; Boyd & Clay
week were reported for bioflocs shrimp culture at 2002). These systems use a similar principle of
similar salinities (Ray et al. 2011). Survival was sludge removal as the WE treatment. However,
above the 49.7% found by Ray et al. (2011) in these values are reported for ponds deeper than
similar culture conditions. Although shrimp sur- the average 0.9-m depth used in the present study
vival in WE (57.8  11.6%) was not significantly (McIntosh 2000). The total water use in WE
different from SE (73.8  1.4%), the greater vari- (53 920 L per tank) was 10% higher than in SE
ability found in the experimental WE units sug- (48 565 L per tank) and, the value of 632 L kg1
gests that water renewal may be associated with of shrimp indicates a 45% increase in water con-
shrimp survival due to the water quality variations servation when related to WE, due to higher final
in this treatment. biomass and lower water use during culture
The differences in mean shrimp weight occurred shown by SE treatment.
after the fifth week, and may have been associated The system operation in SE treatment was sim-
with the greater ammonia variability. The concen- pler and demonstrated some advantages with
trations were not statistically different; however, the use of this technology in larger ponds. Total
the variations in TAN in the WE treatment suspended solids (TSS) production was lower

10 © 2016 John Wiley & Sons Ltd, Aquaculture Research, 1–13


Aquaculture Research, 2016, 1–13 Two methods for solids management in BFT system R Arantes et al.

probably due to the lower P/R ratio and lower Avnimelech Y., Kochva M. & Diab S. (1994) Develop-
FCR observed in this treatment. Also, sludge in the ment of controlled intensive aquaculture systems with
SE units was 13 times more concentrated than a limited water exchange and adjusted carbon to nitro-
that removed from the WE mainly due to com- gen ratio. Israeli Journal of Aquaculture-Bamidgeh 46,
119–131.
pressibility inside the settler (Sharrer, Rishel, Tay-
Bendschneider K. & Robison R.J. (1952) A new spec-
lor, Vinci & Summerfelt 2010). This concentration
trophotometric method for the determination of nitrite
(33  6.1 g L1) is similar to those reported by in sea water. Journal of Marine Research 11, 87–96.
Ray et al. (2011) of between 22 and 27 g L1 Boyd C.E. & Clay J.W. (2002) Evaluation of Belize Aquacul-
when using settlers. ture, Ltd: A Superintensive Shrimp Aquaculture System,
Using both management strategies are efficient pp. 17. Report prepared under the World Bank, NACA,
in controlling biofloc concentrations of the culture WWF and FAO Consortium Program on Shrimp Farm-
water, however, settlers can reduce water use ing and the Environment.
improving sludge solids concentration. The contin- Bratvold D. & Browdy C.L. (1998) Simple electrometric
uous operation of settlers improve solids quality methods for estimating microbial activity in aquacul-
and water quality variables such as ammonia ture ponds. Aquacultural Engineering 19, 29–39.
Browdy C.L. & Moss S.M. (2005) Shrimp culture in
increasing shrimp production.
urban, super-intensive closed systems. In: Urban Aqua-
culture (ed. by B. Costa-Pierce), pp. 173–185. CABI,
Acknowledgments Wallingford, UK.
Browdy C.L., Bratvold D., Stokes A.D. & Mcintosh R.P.
The authors would like to thank to Coordenacß~ ao (2001) Perspectives on the application of closed shrimp
de Aperfeicßoamento de Pessoal de Nıvel Superior culture systems. In: The New Wave, Proceedings of the
(CAPES) for the doctoral fellowship and financial Special Session on Sustainable Shrimp Culture (ed. by C.L.
support (Ci^encias do Mar – CAPES – no. 09/ Browdy & D.E. Jory), pp. 20–34. The World Aquacul-
2009). The authors would also like to thank to ture Society, Baton Rouge, LA, USA.
the Laboratorio de Camar~
oes Marinhos(LCM-USFC) Burford M.A., Thompson P.J., McIntosh R.P., Bauman
and Francisco Pchara for their support in conduct- R.H. & Pearson D.C. (2003) Nutrient and microbial
dynamics in high-intensity, zero-exchange shrimp
ing the experiment.
ponds in Belize. Aquaculture 219, 393–411.
Casillas-Hernandez R., Magall~ aes-Barajas F., Portillo-
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