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Ecological Engineering
journal homepage: www.elsevier.com/locate/ecoleng
A R T I C L E I N F O
A B S T R A C T
Article history:
Received 15 August 2014
Received in revised form 30 January 2015
Accepted 5 April 2015
Available online xxx
The objective of this study was to assess the effect of different solar radiation intensities on nitrogen
assimilation by a consortium of bacteria and microalgae grown in pilot scale high rate ponds (HRP)
treating domestic wastewater. The HRPs received efuent from an anaerobic reactor. The experiment was
carried out under tropical climate conditions. A total of ve HRPs were used; four of them were covered
with shading screens that blocked 9%, 18%, 30% and 60% of the incident solar radiation. Nitrication was
the main process for nitrogen removal/transformation in all HRPs and the volatilization of ammonia
nitrogen occurred in levels below the expected range due to low pH values. The organic nitrogen
concentration followed the same trend of the biomass production, but no statistical difference was found
between the 60% screen HRP and the uncovered one, which led to the conclusion that the intensity of the
photosynthetically active radiation does not compromise nitrogen assimilation, since the bacterial
biomass may develop in conditions that are unfavorable to the growth of microalgae. Moreover, other
aspects, such as CO2 addition, may reduce nitrogen losses by volatilization and denitrication, as well as
contribute to recover this nutrient through biomass assimilation.
2015 Elsevier B.V. All rights reserved.
Keywords:
Nitrogen assimilation by biomass
Microalgae
High rate ponds
Microalgae/bacteria consortium
1. Introduction
Domestic wastewater discharge into water bodies without
proper treatment is among the main sources of nitrogen release in
the environment (Babu et al., 2011). Despite being an essential
component of several biomolecules such as nucleotides and amino
acids, its high availability in the inorganic forms of N-NH4+,
N-NO2 and N-NO3 may result, among other consequences, in the
intensication of the eutrophication process (Camargo and
Alonso, 2006).
Aiming not only at the compliance with discharge standards,
but also at the recovery and use of the nitrogen in human excreta,
the use of microalgae for wastewater bioremediation has gained
signicant importance (Craggs et al., 2011; Rawat et al., 2011;
Olgun, 2012; Arbib et al., 2013; Pires et al., 2013). Microalgae
release oxygen through photosynthesis, which can signicantly
improve the aerobic degradation of the organic matter
141
142
100%
(1)
90%
Relative Abundance
80%
70%
Chlorococcum sp.
60%
Coelastrum sp.
50%
Desmodesmus sp.
40%
Chlorella sp.
30%
Others
20%
10%
0%
HRP controlHRP9% HRP18%HRP30% HRP60%
Fig. 2. Phytoplankton community within the HRPs.
FreeNH3
100
Totalammonianitrogen 1 10f0:090182729:92=T273:20pHg
(2)
Since the paddlewheels provide the constant mixing of the efuent
in the ponds, which characterizes them as complete mix reactors,
the sedimentation process was inexistent.
Two approaches may be used to determine the nitrogen fraction
that has undergone denitrication: direct measurement or
quantication of what has been volatilized, nitried, assimilated
by the biomass or not removed. This study adopted the latter.
2.4. Statistical analysis
The version 2.15.2 of the statistical software R, developed by
the R Foundation for Statistical Computing (R Development Core
Team, 2013) was used to verify the differences among the results of
the variables measured in the ponds.
3. Results and discussion
3.1. Phytoplankton community
The genera Chlorella sp. and Desmodesmus sp. were dominant in
all ponds, during the entire sampling period. In the HRPcontrol,
HRP9%, HRP18%, HRP30% and HRP60%, the average abundances of
Chlorella sp. were 37%, 40%, 37%, 42% and 52%, and of Desmodesmus
sp., these values were 35%, 38%, 45%, 44% and 37%, respectively. The
HRPcontrol presented abundance of Coelastrum sp. and
Micractinium sp. in June (month with lower temperatures); then
Chlorella sp. and Desmodesmus sp. became dominant again. Lower
abundances of Scenedesmus sp., Chlorococcum sp. and Coelastrum
sp. were observed throughout the monitoring period in the
HRPcontrol, and Navicula sp. in the HRP9% and HRP30%, whereas
the genera Ulothrix sp., Euglena sp. and Scenedesmus sp. were only
observed in the HRP60%. Fig. 2 presents the relative abundance of
the main genera found in each HRP.
The aforementioned genera are commonly found in HRPs (Park
and Craggs, 2010; Park et al., 2011a). Sutherland et al. (2014)
Table 1
pH, DO, temperature and PAR in the HRPs and in the efuent from the UASB reactor (mean and standard deviation).
pH
DO (mg L1)
Temperature ( C)
PAR (mE m2 s2)
UASB
HRPcontrol
HRP9%
HRP18%
HRP30%
HRP60%
7.1 (0.34)
1.9 (0.8)
23.9 (1.8)
7.7 (0.72)
6.4 (2.0)
24.3 (2.3)
1087.3 (697.6)
7.8 (0.87)
7.0 (2.4)
23.9 (2.3)
871.5 (577.4)
7.8 (0.88)
8.0 (2.3)
23.7 (2.3)
815.4 (513.4)
7.9 (0.97)
7.4 (2.8)
23.6 (2.2)
707.3 (429)
7.2 (0.99)
6.3 (2.3)
22.8 (2.2)
387.1 (241.4)
100%
143
800
90%
700
80%
600
VSS (mg L-1)
70%
60%
50%
40%
30%
20%
10%
Norg
HRPcontrol
N-NH4+
HRP9%
N-NO3-
HRP18%
HRP30%
Volatilization
400
300
200
100
0%
UASB
500
HRP60%
Denitrification
HRPcontrol
HRP9%
HRP18%
HRP30%
HRP60%
1 Quartile
Max
Med
Min
3 Quartile
7
6
chl a (mg L-1)
5
4
3
2
1
0
HRPcontrol
1 Quartile
HRP9%
Max
HRP18%
Med
HRP30%
Min
HRP60%
3 Quartile
Table 2
Mass balance for the nitrogen in the HRPs.
Forms of N and removal routes (g day1)
UASB
HRPcontrol
HRP9%
HRP18%
HRP30%
HRP60%
Norg
NNH4+
NNO3
Volatilization
Denitrication
2.1
9.9
0.7
0
0
4.1
3
4.2
0.6
0.7
2.9
3.9
4.3
0.8
0.7
2.6
2.6
4.5
0.9
2
3
3.6
3.5
1.2
1.4
3.4
3.3
3.9
0.6
1.5
144
Table 3
VSS and chla productivities and the VSS:chla ratio.
HRP control
HRP9%
HRP18%
HRP30%
HRP60%
11385 (4470)
115 (92)
98
10675 (4625)
99 (66)
112
9508 (3071)
138 (102)
69
10301 (4486)
119 (76)
88
11913 (9845)
74 (63)
163
145
Mata, T.M., Martins, A.A., Caetano, N.S., 2010. Microalgae for biodiesel production
and other applications: a review. Renew. Sustainable Energy Rev. 14, 217232.
Molina Grima, E., Acin Fernndez, F.G., Camacho, F.G., Rubio, F.C., Chisti, Y., 2000.
Scale-up of tubular photobioreactors. J. Appl. Phycol. 12, 355368.
Nederlands Norm (NEN). NEN 6520, 1981, 1981. Water: spectrophotometric
determination of chlorophyll a content. Delft. Nederlands NormalisatieInstituut, The Netherlands (In Dutch).
Olgun, E.J., 2012. Dual purpose microalgae-bacteria-based systems that treat
wastewater and produce biodiesel and chemical products within a Biorenery.
Biotechnol. Adv. 30, 10311046.
Oswald, W.J., 1960. Fundamental factors in stabilization pond design. Proceedings of
3rd Conference on Biological Waste Treatment. Manhattan College, New York.
Park, J.B.K., Craggs, R.J., 2010. Wastewater treatment and algal production in high
rate algal ponds with carbon dioxide addition. Water Sci. Technol. 61 (3),
633639.
Park, J.B.K., Craggs, R.J., 2011. Nutrient removal in wastewater treatment high rate
algal ponds with carbon dioxide addition. Water Sci. Technol. 63 (8), 17581764.
Park, J.B.K., Craggs, R.J., Shilton, A.N., 2011a. Wastewater treatment high rate algal
ponds for biofuel production. Biores. Tecnol. 102, 3542.
Park, J.B.K., Craggs, R.J., Shilton, A.N., 2011b. Recycling algae to improve species
control and harvest efciency from a high rate algal pond. Water Res. 45,
66376649.
Parra, O.O., Gonzalez, M., Dellarossa, V., Rivera, P., Orellana, M., 1982. Manual
taxonmico del toplancton de guas continentales. V-Chlorophyceae
Concepcion (in Spanish).
Peccia, J., Haznedaroglu, B., Gutierrez, J., Zimmerman, J.B., 2013. Nitrogen supply is
an important driver of sustainable microalgae biofuel production. Trends
Biotechnol. 31, 134138.
Pires, J.C.M., Alvim-Ferraz, M.C.M., Martins, F.G., Simes, M., 2013. Wastewater
treatment to enhance the economic viability of microalgae culture. Environ. Sci.
Pollut. Res. 20 (8), 50965105.
Pittman, J.K., Dean, A.P., Osundeko, O., 2011. The Potential of Sustainable algal
biofuel production using wastewater resources. Biores. Technol. 102, 1725.
Prajapati, S.K., Kaushik, P., Malik, A., Vijay, V.K., 2013. Phycoremediation coupled
production of algal biomass, harvesting and anaerobic digestion: possibilities
and challenges. Biotechnol. Adv. 31, 14081425.
R Development Core Team, 2013. A Language and Environment for Statistical
Computing. R Foundation for Statistical Computing, Vienna, Austria [cited Jan
15] Available from 2013; http://www.R-project.org.
Rawat, I., Kumar, R.R., Mutanda, T., Bux, F., 2011. Dual role of microalgae:
phycoremediation of domestic wastewater and biomass production for
sustainable biofuels production. Appl. Energy 88, 34113424.
Renuka, N., Sood, A., Ratha, S.K., Prassanna, R., Ahluwalia, A.S., 2013. Evaluation of
microalgal consortia for treatment of primary treated sewage efuent and
biomass production. J. Appl. Phycol. 25, 15291537.
Ruiz-Martinez, A., Martin Garcia, N., Romero, I., Seco, A., Ferrer, J., 2012. Microalgae
cultivation in wastewater: nutrient removal from anaerobic membrane
bioreactor efuent. Biores. Technol. 126, 247253.
Samori, G., Samori, C., Guerrini, F., Pistocchi, R., 2013. Growth and nitrogen removal
capacity of Desmodesmus communis and of a natural microalgae consortium in
a batch culture system in view of urban waste water treatment: part I. Water
Res. 47, 791801.
Silva, T.L., Gouveia, L., Reis, A., 2014. Integrated microbial processes for biofuels and
high value-added products: the way to improve the cost effectiveness of biofuel
production. Appl. Microbiol. Biotechnol. 98, 10431053.
Subashchandrabose, S.R., Ramakrishnan, B., Megharaj, M., Venkateswarlu, K., Naidu,
R., 2011. Consortia of cyanobacteria/microalgae and bacteria: biotechnological
potential. Biotechnol. Adv. 29, 896907.
Sutherland, D.L., Turnbull, M.H., Craggs, R.J., 2014. Increased pond depth improves
algal productivity and nutrient removal in wastewater treatment high rate algal
ponds. Water Res. 53, 271281.
Toet, A., Huiber, L.H.F.A., Van Logtestijin, R.S.P., Verhoeven, J.T.A., 2003.
Denitrication in the periphyton associated with plant shoots and in the
sediment of a wetlands system supplied with sewage treatment plant efuent.
Hydrobiologia 501, 2944.