Professional Documents
Culture Documents
Miroslava Vivanco-Aranda1, Cristian Jorge Gallardo-EscaŁrate2 & Miguel AŁ ngel del R|¤ o-Portilla1
1
Laboratorio de Gene¤tica, Departamento de Acuicultura, Centro de Investigacio¤n Cient|¤ ¢ca y de Ecuacio¤n Superior de
Ensenada Ensenada, BC, Me¤xico
2
Departamento de Oceanograf|¤ a, Centro de Biotecnolog|¤ a, Universidad de Concepcio¤n, Barrio Universitario s/n Casilla 160-C,
Concepcio¤n, Chile
Correspondence: M A del R|¤ o-Portilla, CICESE, Acuicultura, PO Box 434844, San Diego, CA 92143-4844, USA. E-mail: mdelrio@
cicese.mx
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Recirculating and £ow through red abalone culture M.Vivanco-Aranda et al. Aquaculture Research, 2011, 42, 161^168
objective of this work was to evaluate and compare lasted 4 months, beginning on 9 October 2003 and
the growth rate and survival of red abalone cultured concluding on 13 February 2004. Fifty grams of or-
in a recirculating and in a £ow-through system. ganisms were randomly allocated to each tank. The
initial mean shell length was 5.88 0.04 mm for
abalones maintained in the recirculating system and
Materials and methods 6.21 0.01mm in the £ow-through system. All data
Juvenile abalone are average standard error. Abalones were fed at a
ratio of 70% of abalone weight per week with Macro-
Seven-month-old red abalone (batch 200D, produced cystis pyrifera according to the alimentation of the
by spawning 33 males and 73 females), were obtained abalones in the commercial farms (N. Garc|¤ a, pers.
from the commercial farm ‘Abulones Cultivados S.A. comm.). Every week, macroalgae were removed and
de C.V.’ located in Ejido Ere¤ndira, Baja California, Me¤x- replaced with fresh ones.
ico (31116 03300 N,116122 05300 W). Juvenile abalones were
separated from substrata using CO2 and were trans- Abalone and environmental variable
ported on a wet sponge in plastic bags with oxygen at measurements
the Aquaculture Department (Departamento de Acui-
cultura) at the Centre for Scienti¢c Research and Every 2 weeks, the shell length of 50 randomly se-
Higher Education in Ensenada (Centro de Investiga- lected animals per tank was measured using an elec-
cio¤n Cient|¤ ¢ca y de Educacio¤n Superior de Ensenda, tronic vernier calliper (precision to 0.01mm) model
CICESE). After arriving at our facilities, individual se- S225 (Fowler Company, Newton, MA, USA). Every
paration was not possible; thus, abalone distribution day, temperature and dissolved oxygen were mea-
was based on the weight of several abalones, which sured using an oxymeter model YSI 55 (YSI, Yellow
were then transferred to culture systems. In each tank Springs, OH, USA). On 24 November, in both systems,
50 g of abalones were placed, which corresponds to a a heater (precision of 0.55 1C) model Pro Heat II
low stocking density of 0.070 kg m 2 570 g cm 2 150 W (Won Brother’s, Fredericksburg, VA, USA) was
(2265 organisms m 2). placed to maintain the temperature above 16 1C. Sali-
nity was measured using a temperature-compen-
sated refractometer (conventional refractometer)
Culture systems and pH was measured using a Hanna Hi98127 meter
(Hanna Instruments,Woonsocket, RI, USA). Alkalinity
One £ow-through system and one recirculating sys-
was measured two or three times a week with 1.6 N
tem were used in the growth trial. Three individual
H2SO4 and a bromcresol green-methyl red indicator
£ow-through systems, each one with individual
(Hach Company, Loveland, CO, USA). Because an alka-
water supply plus three individual recirculating sys-
linity concentration between 80 and 200 mg L 1 of
tems, were used. Each one of the recirculating sys-
CaCO3 is optimal for bacterial survival in the bio¢lters
tems consisted of a cylindrical £at-bottom ¢breglass
(Loyless & Malone 1997), when alkalinity values de-
tank (250 L capacity) connected to a magdrive 500
clined below 100 mg L 1 of CaCO3, alkalinity was ad-
pump (Danner Manufacturing, Islandia, NY, USA)
justed to 150 mg L 1 of CaCO3 with the addition of
and a 28.31L (1ft3) bubble wash bead ¢lter (Aquacul-
commercial sodium bicarbonate, Iris quality (Smart
ture System Technologies, New Orleans, LA, USA) as
& Final, Tijuana, BCN, Mexico), to the recirculating
a bioclari¢er (Malone & Beecher 2000), with a back-
systems according to the method described by Loyless
wash frequency of two to three times a week. The
and Malone (1997). The concentrations of TAN, NO2-N
bead ¢lters were acclimated for 60 days at 20 1C be-
and NO3-N were determined two or three times per
fore the experiment as recommended by Malone and
week using a saltwater master liquid test kit (Aqua-
Beecher (2000). In the recirculating systems, the £ow
rium Pharmaceuticals, Chalfont, PA, USA); for colora-
rate was 30 L min 1. The three individual £ow-
tion of each nutrient, the absorbance was read using a
through systems consisted of similar tanks (250 L ca-
spectrophotometer Shimadzu UV-1201 (Shimadzu
pacity) mentioned above. A £ow rate of 1.39 L min l
Scienti¢c Instruments, Columbia, MD, USA).
was set in the three tanks for a daily water exchange
rate of 800%. The water used was pumped from the
Statistical analyses
ocean and ¢ltered to 70 mm before reaching the
tanks. Constant aeration was provided throughout At the beginning of the experiment, abalone shell
the experiment to both systems. The experiment lengths were compared among tanks with an ANOVA
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Aquaculture Research, 2011, 42, 161^168 Recirculating and £ow through red abalone culture M.Vivanco-Aranda et al.
r 2010 CICESE
Aquaculture Research r 2010 Blackwell Publishing Ltd, Aquaculture Research, 42, 161^168 163
Recirculating and £ow through red abalone culture M.Vivanco-Aranda et al. Aquaculture Research, 2011, 42, 161^168
Table 1 Water quality parameters measured in two systems of culture of juvenile red abalones Haliotis rufescens
Temperature, dissolved oxygen, salinity and pH (n 5128). Alkalinity, TAN, nitrite-nitrogen and nitrates-nitrogen (n 5 45).
lower dissolved oxygen concentration (n 5128, obtained in this study were similar to other GR/ISL
t 513.51, Po0.001) and higher salinity (n 5128, values. Furthermore,Table 3 shows a comparison be-
t 5 2.45, P 5 0.016). tween studies carried out with arti¢cial diets against
Alkalinity and pH were signi¢cantly di¡erent be- macroalgae with other abalone species. The highest
tween systems (Table 1) due to the addition of sodium growth rates in most of these works were achieved
bicarbonate in the recirculating system, where alkali- by feeding abalones with an arti¢cial diet. This may
nity and pH were higher (n 5 45, t 511.2, Po0.001; be explained by the fact that both the arti¢cial diets
n 5128, t 5 25.8, Po0.001 respectively). had higher protein and fat contents and produced
There were no di¡erences between systems with the best growth rates in terms of the total weight
TAN (n 5 45, t 5 0.45, P 5 0.66) and NO3-N and shell length (Capinpin & Corre1996), which sug-
(n 5 45, t 5 0.94, P 5 0.35) between systems (Table 1). gests that diet type has a direct e¡ect on abalone
growth rate.
In contrast to this study, for other abalone species of
similar sizes growth rates of the100 mm day 1 growth
Discussion
rate of similar abalone size were obtained with aba-
Abalone growth is in£uenced by environmental con- lone juveniles of Haliotis tuberculata (Linnaeus, 1758)
ditions, water quality (Leitman 1992; Hoshikawa, Sa- fed with an arti¢cial diet (Lopez et al. 1998) and with
kai & Kijima 1998; Harris, Maguire, Edwards & Johns Japanese abalone Haliotis discus hannai Ino,1953 (Hos-
1999), diet type (Viana, Cervantes-Trujano & Solana- hikawa et al. 1998) fed with diatoms. The highest
Sansores 1994; Capinpin Jr & Corre 1996; Viana, growth rates have been reported in juveniles between
Cervantes-Trujano & Solana-Sansores 1996; Haaker, 10 and 40 mm shell length in other abalone species:
Parker, Barsky & Chun 1998; Lopez, Tyler & Viana Haliotis asinina Linnaeus, 1758 (Capinpin & Corre,
1998; Bautista-Teruel & Millamena 1999; Capinpin Jr, 1996; Fermin 2002), black abalone Haliotis cracherodii
Toledo, Encena & Doi 1999), culture density (Day & Leach, 1814 (Leighton & Boolootian 1963), paua aba-
Fleming 1992; Mgaya & Mercer 1995; Mgaya, Gosling, lone Haliotis iris Gmelin, 1791 (Clarke & Creese 1998),
Mercer & Donlon 1995; Clarke & Creese 1998; Valdes- H. fulgens (Leighton, Byhower, Kelly, Hooker & Morse
Urriolagoitia 2000) and abalone size at the beginning 1981), greenlip abalone Haliotis laevigata Donovan,
of the experiment (Corazani & Illanes 1998; Trevel- 1808 (Gilroy & Edwards 1998) and H. tuberculata (Lo-
yan, Mendoza & Buckley 1998; Steinarsson & Ims- pez et al.1998), all fed with an arti¢cial diet.
land 2003). Abalone size is a principal factor An other aspect that a¡ects the growth rate is the
a¡ecting the feeding rates of gastropods. Generally, culture density. For abalone cultured in £ow-through
feeding rates per biomass unit are higher in smaller systems, growth is inversely related to density
and faster growing juveniles than in larger abalone (Mgaya & Mercer1995; Capinpin et al.1999;Valde¤s-Ur-
(Marsden & Williams, 1996). riolagoitia 2000). Culture density has an inverse ef-
H. rufescens fed with arti¢cial diets and di¡erent fect on abalone survival and may a¡ect abalone
types of macroalgae produce similar growth rates growth directly through competition for food
as macroalgae (Table 2). It can be observed that red and space. However, in this study, density was not a
abalone growth rate/initial shell length (GR/ISL) critical factor for the growth rate because a low
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Aquaculture Research, 2011, 42, 161^168 Recirculating and £ow through red abalone culture M.Vivanco-Aranda et al.
Table 2 Data from di¡erent studies on the growth juvenile red abalones Haliotis rufescens
Initial shell length (ISL) is the average length of the abalone’s shell in the beginning of the experiment and growth rate (GR) is the
monthly growth of the abalones shell (evaluated in millimetres).
Table 3 Data of di¡erent relating experimental studies for the growth juvenile of diverse species
Haliotis fulgens 10.00 2.71 0.271 Egregia laevigata and Leighton et al. (1981)
25.00 1.74 0.070 Macrocystis pyrifera
42.00 0.71 0.017
Haliotis tuberculata 15.30 1.75 0.114 Palmaria palmata Mgaya and Mercer (1995)
15.20 1.07 0.070
19.60 1.61 0.082
23.80 1.67 0.070
16.80 1.81 0.108
Haliotis asinina 15.80 4.07 0.258 Gracilaria bailinae Bautista-Teruel and Millamena (1999)
15.20 6.67 0.439 Artificial diet
15.80 7.33 0.464 Artificial diet
15.90 7.43 0.467 Artificial diet
Haliotis asinina 19.00 4.20 0.221 Gracilaria heteroclada Capinpin et al. (1999)
Haliotis rubra 33.91 1.30 0.038 Artificial diet Huchette et al. (2003)
34.23 0.90
Present study
Haliotis rufescens 5.88 0.78 0.133 Macrocystis pyrifera Recirculating system
6.21 0.67 0.108 Flow through system
Initial shell length (ISL) is the average length of the abalone’s shell in the beginning of the experiment and growth rate (GR) is the
monthly growth of the abalones shell (evaluated in millimetres).
stocking density was used for both culture systems to Also, the di¡erences may be due to the size of the or-
eliminate potential complications due to a high stock- ganisms and the duration of the experiment. There-
ing rate. The low stocking density used in this study fore, it is possible to obtain high growth rates of H.
can explain the highest survival rate obtained com- rufescens even on feeding with macroalgae if the phy-
pared with the survival rates reported in other stu- sical^chemical variables are within the ranges of
dies (Nie, Ji & Yan 1996, Park, Rho & Song 1995). good water quality and low stocking density.
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Mortality not only depends on the culture density Table 4 Cost analysis of the two systems of culture of juve-
but also on inadequate handling (stress) of food nile red abalones Haliotis rufescens
transfer (Searcy-Bernal, Salas-Garza & Flores-Agui-
lar 1992). The mortality rate is also associated with Cost (US$)
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Aquaculture Research, 2011, 42, 161^168 Recirculating and £ow through red abalone culture M.Vivanco-Aranda et al.
tion of H. rufescens in recirculation culture systems. growth of abalone, Haliotis asinina (Linnaeus). Aquacul-
With the present work, it is possible to state that recir- ture Research 33,197^202.
culating systems are a feasible alternative for the Gilroy A. & Edwards S.J. (1998) Optimum temperature for
culture of juvenile red abalone at a low density. growth of Australian abalone: preferred temperature
and critical thermal maximum for blacklip abalone, Ha-
liotis rubra (Leach), and greenlip abalone, Haliotis laeviga-
ta (Leach). Aquaculture Research 29, 481^485.
Acknowledgments Haaker P.L., Parker D.O., Barsky K.C. & Chun C.S.Y. (1998)
Growth of red abalone, Haliotis rufescens (Swainson), at
The CONACYT supported the M.Sc. studies of M.V.-A.
Johnsons Lee, Santa Rosa Island, California. Journal of
with a scholarship. This study was partially ¢nanced
Shell¢sh Research 17,747^753.
by means of the CONACYT project ‘Genetic markers Harris J.O., Maguire G.B., Edwards S.J. & Hindrum S.M.
of abalone, Haliotis spp.’ (33018 B) and by CICESE pro- (1997) E¡ect of nitrite on growth and oxygen consump-
ject number 655. The authors are particularly grate- tion for juvenile greenlip abalone, Haliotis laevigata Dono-
ful to the commercial farm ‘Abulones Cultivados S.A. van. Journal of Shell¢sh Research 160, 395^401.
de C.V.’ for providing the abalone used in this research. Harris J.O., Maguire G.B., Edwards S.J. & Hindrum S.M.
The authors also thank Marisela Aguilar-JuaŁrez for (1998) E¡ect of ammonia on the growth rate and oxygen
the support provided and Oscar B. Del R|¤ o Zaragoza consumption of juvenile greenlip abalone, Haliotis laevi-
for the technical assistance. gata Donovan. Aquaculture 160, 259^272.
Harris J.O., Maguire G.B., Edwards S.J. & Johns D.R. (1999)
Low dissolved oxygen reduces growth rate and oxygen
consumption rate of juvenile greenlip abalone, Haliotis
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