Acta Biológica Colombiana
0120-548X
Universidad Nacional de Colombia, Facultad de Ciencias, Departamento de Biología
https://doi.org/10.15446/abc.v23n3.69537

Recibido: 20 de diciembre de 2017; Revision Received: 22 de junio de 2018; Aceptado: 25 de julio de 2018

GRUPOS FUNCIONALES FITOPLANCTÓNICOS EN UNA LAGUNA ALGAL DE ALTA TASA USADA PARA LA BIORREMEDIACIÓN DE LIXIVIADOS DE RELLENOS SANITARIOS

Phytoplankton Functional Groups in a High-Rate Algal Pond Used for the Bioremediation of Landfill Leachate

A. SAAVEDRA, 1 * C. PARRA, 2E. SALAMANCA, 1V. CERÓN, 3J. MOSQUERA, 4

Grupo Biología de Plantas y Microorganismos, Departamento de Biología, Facultad de Ciencias Naturales y Exactas, Universidad del Valle. Calle 13 n°. 100-00. Cali, Colombia. Universidad del Valle Departamento de Biología Facultad de Ciencias Naturales y Exactas Universidad del Valle Cali Colombia
Grupo de Saneamiento Ambiental, Escuela de Ingeniería de los Recursos Naturales y del Ambiente (EIDENAR), Facultad de Ingeniería, Universidad del Valle. Calle 13 n°. 100-00. Cali, Colombia. Universidad del Valle Escuela de Ingeniería de los Recursos Naturales y del Ambiente (EIDENAR) Facultad de Ingeniería Universidad del Valle Cali Colombia
Grupo de Saneamiento Ambiental, Instituto Cinara. Universidad del Valle, Calle 13 n°. 100-00, Cali, Colombia. Universidad del Valle Grupo de Saneamiento Ambiental, Instituto Cinara Universidad del Valle Cali Colombia
Escuela de Estadística, Facultad de Ingeniería, Universidad del Valle, Calle 13 n°. 100-00, Cali, Colombia. Universidad del Valle Facultad de Ingeniería Universidad del Valle Cali Colombia

For correspondence. antonellasardi06@gmail.com

RESUMEN

El análisis de comunidades fitoplanctónicas utilizando el enfoque de grupos funcionales (GF), es empleado para predecir la respuesta de la composición de especies fitoplanctónicas a la variación de las condiciones ambientales. El objetivo de este estudio fue evaluar por primera vez bajo condiciones de trópico americano la dinámica de los grupos funcionales de fitoplancton asociados a un sistema de laguna algal de alta tasa fotosintética (LALAT), empleada para la biorremediación de lixiviados de rellenos sanitarios, utilizando la propuesta de grupos funcionales basada en la morfología (MBFG). Se tomaron muestras de agua para análisis biológico y fisicoquímico durante siete meses. Adicionalmente, se calculó el biovolumen del fitoplancton y se realizó un análisis de correlación canónica para explicar la relación entre las variables físicoquímicas y los grupos funcionales. La LALAT trató un lixiviado de edad intermedia caracterizado por altas concentraciones de nutrientes. Se identificaron cuatro MBFG (IV, V, VI y VII). El grupo V, conformado por fitoflagelados, fue dominante durante todo el periodo de estudio. Este grupo puede sobrevivir y proliferar en ambientes con altas concentraciones de materia orgánica. Además, contribuye a la transformación de los contaminantes presentes en el lixiviado. El aumento del biovolumen de los grupos V y VII se relacionó con los periodos en los cuales la laguna presentó los menores valores de carbono orgánico disuelto. Finalmente, se encontró que el enfoque de los MBGF puede ser útil para comprender la dinámica de la comunidad de fitoplancton en la LALAT utilizado para el tratamiento de lixiviados en rellenos sanitarios.

Palabras clave:

grupos funcionales, lixiviados, microalgas.

ABSTRACT

The functional group (FG) approach is used to predict the response of the composition of phytoplankton species to changes in the environmental conditions. We assessed for the first time the dynamics of phytoplankton communities in a High-Rate Algal Pond (HRAP), implemented for the bioremediation of landfill leachate, and using morphology-based functional groups (MBFG), under the American tropics conditions. These groups were later correlated with the physical and chemical variables of the system. Water samples were taken for biological, physical and chemical analysis for seven months. In addition, phytoplankton biovolumes were estimated and a canonical correlation analysis was performed to explain the relation between physical and chemical variables and FGs. Subsequently, the HRAP treated a medium-age leachate characterized by high concentrations of nutrients. Four MBFGs were identified (IV, V, VI and VII). Group V, conformed by phytoflagellates, was found to be dominant during the entire study period. This group proliferate in environments with high concentrations of organic matter, while contributing to the transformation of the contaminants present in the leachate. The largest biovolumes of Groups V and VII occurred during periods of low water levels and dissolved organic carbon. Finally, we show that the MBFG technique may be useful in understanding the dynamics of the phytoplankton community in the HRAP used for the treatment of landfill leachate.

Keywords:

functional groups, landfill leachate, microalgae.

INTRODUCTION

Functional groups (FGs) are groups of species with similar morphology and physiology that also respond similarly to a set of environmental conditions, without the individuals necessarily belonging to the same phylogenetic group (Reynolds et al., 2002). This model constitutes an efficient tool that better predicts the effect of environmental changes on the organisation of the phytoplankton community than taxonomy-based studies (Kruk and Segura, 2012; Sutherland et al., 2017).To predict changes in the environmental gradients of aquatic ecosystems, FGs was proposed by Margalef (1978) as an adaptation response of lifeforms to stability and nutrient content. Reynolds (2002) proposed a classification based on morphological and physiological characteristics, thus establishing 31 FGs, which were later updated by Padisák et al. (2009). Kruk et al. (2010) proposed a new classification of FGs based on morphology (MBFG), and divided the phytoplankton community into seven groups on the basis of morphological characteristics, such as volume and the presence of a flagellum or silica exoskeleton. Morphological characteristics are related to the functional properties of phytoplankton (Kruk et al., 2010). For example, the size and shape of phytoplankton cells affect growth, metabolism and resource acquisition (Litchman and Klausmeier, 2008).

Although FGs have been studied in natural environments, research has not yet been conducted on FGs in landfill treatment under American tropical conditions. Landfill leachate is a complex wastewater generated by the percolation of rainwater through waste and by the different biochemical reactions that occur within the waste mass of the landfill. Generally, landfill leachate contains biodegradable and non-biodegradable organic matter, nutrients, heavy metals and recalcitrant and xenobiotic compounds (Renou et al., 2008; Madera et al., 2015). Different technological alternatives have been used for landfill leachate treatment. However, little research has been conducted on the use of natural systems, particularly those that employ algal biomass.

Algal ponds are referred to as 'high-rate systems' based on improved biomass yield or productivity and their capacity to treat wastewater (García et al., 2000; Valigore, 2011). High-rate algal ponds (HRAPs) facilitate the treatment of wastewater through the high production of algal biomass and dissolved oxygen by means of a high photosynthetic rate. Thus, they provide a favourable aerobic environment for bacteria to degrade organic matter (Pagand et al., 2000; Park and Craggs, 2010; Sardi-Saavedra etal., 2016). In addition, nutrients, organic matter and suspended solids diminish as a result of the combination of physical and chemical and biological processes, such as sedimentation, precipitation and microbial transformation (Kumar and Zao, 2011).

Millán et al. (2014) analysed FGs on the basis of the functional characteristics of phytoplankton communities associated with two pools intended for the treatment of fish-farm wastewater. A total of 11 Reynold's FGs groups were identified, of which F and P were the most representative. The researchers also noted that the number of FGs decreased at the outlet of the treatment systems, where S1, W1, and H1 were conserved, because they were characteristic of eutrophic environments. Li et al. (2015) found 22 FGs on the basis of functional characteristics in a eutrophic reservoir, where groups S1, D and J predominated. Southerland et al. (2017), suggested that microalgal functional groups helped to understand the ecology of wastewater treatment and biomass production in full-scale HRAP better than individual species did. They found that group J, consisting of mainly non-gelatinous, non-motile Chlorococcales, was the dominant group in the HRAP. However, this type of research is still emerging, and further analysis is needed.

In High-Rate Algal Ponds, algal organisms perform contamination-treatment processes during which organic matter and nutrients are utilised by bacteria, algae and other organisms (Peña et al., 2005). However, the dynamics of the algal community is unknown. Additionally, although Sardi-Saavedra et al. (2016) applied an appropriate ecological approach, a number of areas in this field require clarification ( Peña et al., 2012; Sardi-Saavedra et al., 2016), including the analysis of FGs in the treatment of landfill leachate. Phytoplankton functional groups have not been studied in constructed systems such as a HRAP treated intermediate landfill leachate. In these hypereutrophic systems, phytoplankton community is specific, but its ecological function is not well known, so the application of models of functional groups helps to understand their dynamics. This study will allow understanding the functional ecology of these systems and will provide better information for further best design. In addition, it allows a fast evaluation of the functioning of the systems without the necessity to measure other variables that take time and are costly. Thus, the purpose of this study is to assess for the first time the dynamics of phytoplankton communities in an HRAP used for the bioremediation of landfill leachate through the identification of FGs and the correlation of such groups with the physical and chemical water characteristics.

MATERIALS AND METHODS

Study area

An HRAP was installed within the premises of the Regional Presidente landfill, located in the municipality of San Pedro, Valle del Cauca, Colombia (3°56x01.54" N and 76°26'26.05" W) (Fig. 1). The area has an average temperature of 24.3 °C, a precipitation of 2.3 mm.d-1 and a relative humidity of 74.8 %.

Location of the study unit. Leachate pond and High-rate algal pond.

Figure 1: Location of the study unit. Leachate pond and High-rate algal pond.

The HRAP was designed with the characteristics shown in Table 1. The system received the effluent of a technological coupling that consisted of a High Rate Anaerobic Pond (HRAP) and a subsurface horizontal flow constructed wetland on a pilot scale that treated leachate (2 m3d-1) from the Regional Presidente landfill. The landfill receives approximately 490 T d-1 of solid waste, of which nearly 77 % corresponded to organic matter. In addition, in the landfill, between 2 and 5 L s-1 of leachate were generated (Bugaseo, 2009).

Table 1: HRAP characteristics.

Shape Raceway configuration (oval)
Flow 0.24 m3d-1
Hydraulic Retention Time (HRT) 2 d
Superficial Organic Load 6. 5 g m-2d-1
Volume 0.3 m3
Width 0.6 m
Length 2.4 m
Height m

Physical and chemical characteristics

HRAP sampling and data generation were performed at a depth of 0.05 m from the pond surface. The following physical and chemical parameters in the water samples were measured: phosphates (PO4 -3 -P), total suspended solids (TSS), volatile suspended solids (VSS), dissolved organic carbon (DOC), total chemical oxygen demand (COD) and filtered COD (filtered COD), total Kjeldahl nitrogen (TKN), N-NH4+ (ammoniacal nitrogen) and N-NO3 - (nitrates) in accordance with APHA (2012) and IDEAM (2009). Similarly, data related to temperature, pH, and dissolved oxygen (DO) were recorded in situ using a WTW 340i multi-parameter portable meter. Finally, chlorophyll a was determined using an AquaFluor® Handheld Fluorometer and Turbidimeter.

Biological samples

Algal samples were grabbed fortnightly between January and July 2013 except in March and April because the operating HRAP system was not working. These systems are not controlled by the seasonal regime, and their dynamics is associated to the operation of the treatment systems. Approximately 500 ml samples were collected in plastic containers at the pond's centre. We filtered 500 ml of sample and we homogenized this amount of volume to be able to be count. The samples were fixed with 10 ml formaldehyde (4 %) as a preservative following the recommendations by Zaixso (2002). Relevant organisms were identified using the keys and taxonomic descriptions provided by Tell and Conforti (1986), Wehr and Scheath (2003) and Bicudo and Menezes (2006) up to the lowest possible taxonomic level. Additionally, photos were taken and sent to specialists for taxonomic confirmation.

Phytoplankton biovolume was estimated according to the geometric equations proposed by Hillebrand et al. (1999). For phytoplankton quantification, a Sedgwick-Rafter camera was used, and counting was performed using a Nikon Eclipse TS100 inverted microscope following the methods employed by Villafane and Reid (1995) and Wetzel and Likens (2000). To count phytoplankton, the formula proposed by Wetzel and Likens (2000) was used:

Where:

N: Number of organisms /ml

C: Number of organisms

A: Area of the counting chamber (mm2)

a: Area of the ield or band (mm2)

S: Number of ields or bands counted

V: Volume of the counting chamber (ml)

To classify the phytoplankton organisms into the morphology-based functional groups we followed the method proposed by Kruk et al. (2010).

Data analysis

We considered the physical and chemical parameters established in the Colombian environmental regulations (Resolution No. 0631 of 2015, Ministry of Environment and Sustainable Development) to assess the relationships with the biovolumes of the algal populations. Additionally, we conducted an exploratory data analysis and canonical correlation analysis (CCA) to identify associations between a first set of Y1 independent variables (i.e., physical and chemical variables) and a second set of Y2 variables (i.e., total biovolume of each MFFG in one sample) in the seven month of the study. For the implementation, the tools available in XLSTAT 2018.5 (2018) software were applied.

RESULTS

Water quality

The results for the physical and chemical parameters are summarised in Table 2. Water pH was always alkaline, the values remaining over 8.1 all times along the study period. Additionally, the temperature was suitable for algal growth (between 25° C and 33° C). The pond exhibited aerobic reactor behaviour, reaching an average DO concentration level of 9.1 mg L-1. Chlorophyll a monitoring during the time of the study revealed a stable system, reaching concentrations up to 3659 ug L-1. Nutrients exhibited high levels: PO4 3- up to 5.28 mg L-1, NH4+ up to 131 mg L-1 and NO3 - up to 15 mg L-1. Because the HRAP treated a medium-age leachate, whose main characteristic is a high concentration of nutrients, these conditions were expected (Renou et al., 2008) and obtained in the present study.

Table 2: Physicochemical variables in the HRAP during the study period. Where: DOC (Dissolved organic carbon), PO43- (Phosphates), COD (Total chemical oxygen demand), Filtered COD (chemical oxygen demand in the filtered water), TSS (total suspended solids), VSS (volatile suspended solids), TKN (total Kjeldahl nitrogen), NH4+ (ammoniacal nitrogen), NO3- (nitrates), DO (dissolved oxygen) and T (temperature).

Morphology-based functional groups

Overall, 26 morphospecies were recorded, distributed into six phyla and 20 genera (Table 3). Among the seven MBFGs proposed by Kruk et al. (2010), only four groups (IV, V, IV and VII) were found in the HRAP (Table 3). Of these MBFGs, Group V exhibited the largest number of species (14), followed by Group VI (six), Group IV (five) and VII had one specie. When considering abundance alone, Group V was dominant throughout the study period, accounting for 98 % of the total individuals sampled. In terms of biovolume, Group V exhibited the same dominant pattern (Fig. 2).

Total FG biovolumes in the HRAP during the study period.

Figure 2: Total FG biovolumes in the HRAP during the study period.

Table 3: Proposed FGs in the HRAP during the study period.

When assessing the dynamics of the biovolume of the MBFGs throughout the study period, Group V showed a high fidelity, being present in ten samples. Group V was also the dominant group, its biovolume accounting for more than 65 % in each studied month. In contrast, Group IV was present in five samples and groups VI and VII occurred in four of the samples. Group VII appeared in less than 5 % of all samples, whereas Group VI reached 31 % of the total biovolume for January and 27 % for February (Fig. 3).

Phytoplankton biovolume (%) in the HRAP during the study period.

Figure 3: Phytoplankton biovolume (%) in the HRAP during the study period.

Correlation between the MBFG and the physical and chemical water characteristics

The first two factors of the CCA factorial decomposition summarized the variables analysed. They accounted for 82.3 % of the total observed variability (F1 36.3 % and F2 45.8 %). Figure 4 shows the simultaneous representation of a set of Y1 and Y2 variables in the two factorial axes. The two factors, F1 and F2, display a negative relationship with all the variables of the study. The graph also shows that the biovolumes of MBFGs V and VII relate to the periods during which the pond had low levels of DOC. The biovolumes of the MBFG VI related to low levels of fil COD and NH4+. Additionally, the biovolume of IV relate to TKN increases in the pond.

CCA of the FG biovolumes in the HRAP during the study period.

Figure 4: CCA of the FG biovolumes in the HRAP during the study period.

DISCUSSION

The richness of MBFGs recorded in this study was lower than that observed by other authors, such as Petar et al. (2014), Santos et al. (2014) and Mihaljevi et al. (2015). In this regard, Santos et al. (2014) and Mihaljevi et al. (2015) reported seven FGs, whereas Petar et al. (2014) reported five groups. In our study, we reported only four groups (Table 4). This lower MBFG richness may be related with the type of treated water, while the previously mentioned studies were performed in rivers and natural lakes in temperate climates. In the present study, landill leachate was treated under American tropical conditions and thus involved a substantially different between the physical and chemical characteristic of landill leachate compared with natural water bodies.

Table 4: Comparison with the MBFGs found in other studies.

In our research, the pond was alkaline throughout the entire study period, this situation can be related with the biological activity inside the landill and also indicates high photosynthetic activity. Consequently, high DOC concentrations of were found, which facilitated the continuous growth of important heterotrophic bacteria for the degradation of organic matter (Park and Craggs, 2011). In addition, high phosphate, nitrite and nitrogen levels resulted in an increase in the primary production and potential inhibitions that potentially affected the function, structure and dynamics of the pond's algal community. Similarly, it can contribute to high algal productivity, which could be exploited as animal feed or for biodiesel production once the material is harvested.

The HRAP was dominated by Group V, which consists of phytoflagellate species, many of which exhibit mixotrophic behaviour, acting as heterotrophs or autotrophs depending on the conditions. This behaviour represents a significant advantage with respect to the reduction of the organic matter and nutrients present in leachate. In addition, mixotrophic mobility favours movement towards light when this resource is limited or away from light when this resource is abundant (Litchman and Klausmeier, 2008). However, the growth of these organisms reduces light availability for other species. This phenomenon would explain the abundance of Group V throughout the study and the presence, although in smaller proportion, of Groups IV, VI and VII, which are adapted to survive at low light levels (Litchman and Klausmeier, 2008).

Group V is characterised by species that adopt different strategies. For example, some species of the phylum Cryptophyta are regarded as C-strategists. That is, they are small organisms capable of quickly exploiting the available resources and tolerating environmental changes (Reynolds, 1988). In contrast, the S-strategists Chlamydomonas and Euglenophyta grow in more stable, warmer conditions and proliferate in extremely high concentrations of organic matter, such as wastewater (Padisák et al., 2009). In our study, the prevalence of Group V species coincided with the high contaminant loads present in the leachate. It is possible that these strategic differences reflect different hydrological conditions throughout the study period, which can be regarded as a disadvantage when predicting changes in the environmental conditions.

Although represented by few individuals, the other groups displayed adaptation mechanisms that enabled them to resist the high nutrient concentration in the pond. Group VII individuals had mucilage that acted as a mechanical and chemical defence against predators, and their decreased nutrient absorption acted as a population regulatory mechanism while offering floating properties (Margalef, 1978). This group has a preference for high-temperature lakes with a high trophic status (Kruk and Segura, 2012). Group VI, which consists of diatoms, depends on water turbulence (Litchman and Klausmeier, 2008) and easily adapts to low-light conditions and eutrophic environments (Reynolds et al., 2002). Although Group VI exhibited an ample range of responses to trophic status (Reynolds et al., 2002), its members are better competitors in lower temperature conditions (Kruk and Segura, 2012). In contrast, Group IV would not be dominant but can survive under such conditions of high turbulence, excess nutrients and low-light levels (Kruk and Segura, 2012).

Finally, when correlating biovolumes with the physical and chemical characteristics of the water pond, we found that MBFGs V and VII were associated with the periods during which the pond had low levels of DOC. This correlation indicates that under low contaminant concentration conditions in leachate the HRAP new groups appeared, increasing its capacity to reduce such contaminants. Therefore, it is possible to produce an effluent with a low pollution load, which may entail a better performance of the pond. In addition, the biovolume of Group IV was favoured by an increase in TKN in the pond, possibly implying a better capacity for nitrogen assimilation in this group. Lastly, different analyses revealed no association between the levels of fil COD, NH4+ and DOC and the levels of TKN, which indicates that the MBFGs that are favoured by high levels of these variables may well be present simultaneously.

CONCLUSIONS

The HRAP was inhabited by four phytoplankton MBFGs (IV, V, VI y VII) during the study period. These groups were associated with the physical and chemical characteristics of the landfill leachate. Group V formed by the phytoflagellates, was the group with more fidelity and biovolume in this study. This group plays a fundamental role in this system because it is resistant to high concentrations of organic matter and can thrive in this environment. Therefore this group could generate favourable conditions for the reduction of organic matter and nutrients that contribute to the transformation of the contaminants present in the leachate. On the other hand, the HRAP used to treat medium-aged leachates displayed a high richness of MBFGs, which contributed to the reduction and transformation of pollutants. This MBFG richness was related to and depended on the physical and chemical quality of water. Finally, the MBFG technique is useful for understanding the dynamics of the phytoplankton community in the HRAP and also use as a potential tool for influent water quality.

Acknowledgements

ACKNOWLEDGEMENTS

We would like to thank Colciencias and the University of Valle for their economic support through the programme. Young Researchers and Innovators (Jóvenes Investigadores e Innovadores). We are also grateful to BUGASEO S.A. E.S.P. for its economic and infrastructure support and for making it possible for us to conduct our research at the Regional Presidente landfill.

REFERENCES

  1. American Public Health Association (APHA), American water works Association (AWWA) and Water Pollution Control Federation (WPCF). Standard methods for the examination of water and wastewater. Washington: APHA; 2012. 1496 p. 🠔
  2. Bugaseo S.A. ESP. Informe del sistema de tratamiento de lixiviado-Relleno sanitario de Presidente, Buga, Colombia, 2009. 19 p. 🠔
  3. Bicudo CE, Menezes N. Géneros de algas de aguas continentales Do Brasil. Chave para identificacao e descrições. 2nd ed. Sao Paulo: RIMA; 2006. 512 p. 🠔
  4. García J, Hernández-Mariné M, Mujeriego R. Influence of phytoplankton composition on biomass removal from high-rate oxidation lagoons by means of sedimentation and spontaneous flocculation. Water Environ Res. 2000;72(2):230-237. Doi:10.2175/106143000X137392. [DOI] 🠔
  5. Hillebrand H, Durselen CDD, Kirschtel U, Pollingher T, Zohary T. Biovolume calculation for pelagic and benthic microalgae. J Phycol. 1999;35:403-424. Doi:10.1046/j.1529-8817.1999.3520403.x. [URL] 🠔
  6. IDEAM. Procedimiento para el muestreo de aguas y sedimentos para determinación de metales. Bogotá: Subdirección de Estudios Ambientales, Instituto de Hidrología, Meteorología y Estudios Ambientales; 2009. 11 p. 🠔
  7. Kruk C, Huszar VLM, Peeters ETHM, Bonilla S, Costa L, Lurling M, et al. A morphological classification capturing functional variation in phytoplankton. Freshw Biol. 2010;55(3):614-627. Doi:10.1111/j.1365-2427.2009.02298.x. [DOI] 🠔
  8. Kruk C, Segura AM. The habitat template of phytoplancton morphology-based functional groups. Hydrobiologia. 2012;698(1):191-202. Doi:10.1007/s10750-012-1072-6. [DOI] 🠔
  9. Kumar JLG, Zao YQ. A review on numerous modeling approaches for effective, economical and ecological treatment wetlands. J Environ Manag. 2011;92(3):400-406. Doi:10.1016/j.jenvman.2010.11.012. [DOI] 🠔
  10. Li L, Li QH, Jiao SL, Li Y, Xiao J, Deng L, et al. Response of phytoplankton functional groups to eutrophication in summer at Xiaoguan reservoir. Huan Jing Ke Xue. 2015;36(12):4436-4443. Doi:10.13227/j.hjkx.2015.12.015. [DOI] 🠔
  11. Litchman E. Klausmeier CA. Trait-based community ecology of phytoplankton. Annu Rev Ecol Evol Syst. 2008;39:615-639. Doi:10.1146/annurev.ecolsys.39.110707.173549. [DOI] 🠔
  12. Madera-Parra C, Peña-Salamanca E, Peña M, Rousseau D, Lens P. Phytoremediation of landfill leachate with Colocasia esculenta, Gynerum sagittatum and Heliconia psittacorum in Constructed Wetlands. Int J Phytoremediation. 2015;17:37-41. Doi:10.1080/15226514.2013.828014. [DOI] 🠔
  13. Margalef R. Life forms of phytoplankton as survival alternatives in an unstable environment. Oceanologica Acta. 1978;1:493-509. 🠔
  14. Mihaljević M, Stević F, Špoljarić D, Žuna Pfeiffer T. Spatial pattern ofphytoplankton based on the morphology-based functional approach along a river-floodplain gradient. River Res Applic. 2015;31:228-238. Doi:10.1002/rra.2739. [DOI] 🠔
  15. Padisák J, Crossetti LO, Naselli-Flores L. Use and misuse in the application of the phytoplankton functional classification: A critical review with updates. Hydrobiologia. 2009;621:1-19. Doi:10.1007/s10750-008-9645-0. [DOI] 🠔
  16. Pagand P, Blancheton JP, Lemoalle J, Casellas C. The use of high rate algal ponds for the treatment of marine effluent from a recirculating fish rearing system. Aquaculture. 2000; 31:729-736. Doi:10.1046/j.1365-2109.2000.00493.x. [DOI] 🠔
  17. Peña EJ, Palacios ML, Ospina-Álvarez N. Algas como indicadoras de contaminación. 1st ed. Cali: Ediciones Universidad del Valle; 2005. 164 p. 🠔
  18. Peña EJ, Cantera JR, Muñoz E. Evaluación de la Contaminación en Ecosistemas Acuáticos. Estudio de caso en la laguna de Sonso, Cuenca alta de río Cauca, Cali, Colombia. 1st ed. Cali: Programa Editorial Universidad del Valle; 2012. 311 p. 🠔
  19. Petar Z, Marija GU, Koraljka KB, Andelka PM, Padisak J. Morpho-functional classifications of phytoplankton assemblages of two deep karstic lakes. Hydrobiologia, 2014;740:147-166. Doi:10.1007/s10750-014-1950-. [DOI] 🠔
  20. Renou S. Givaudana JG, Poulain S, Dirassouyan F, Moulin P. Landfill leachate treatment: Review and opportunity. J Hazard Mater. 2008;150:468-493. Doi:10.1016/j.jhazmat.2007.09.077. [DOI] 🠔
  21. Reynolds CS. The concept of ecological succession applied to seasonal periodicity of freshwater phytoplankton. Verhandlungen Internationale Vereinigung fur theoretische und angewandte Limnologie. 1988;23:683-691. Doi:10.1080/03680770.1987.11899692. [DOI] 🠔
  22. Reynolds CS, Huszar V, Kruk C, Naselli-Flores L, Melo S. Towards a functional classification of the freshwater phytoplankton. J Plankton Res. 2002;24:417-428. Doi:10.1093/plankt/24.5.417. [DOI] 🠔
  23. Santos AMC, Carneiro FM, Cianciaruso MV. Predicting productivity in tropical reservoirs: The roles of phytoplankton taxonomic and functional diversity. Ecol Indic. 2015;48:428-435. Doi:10.1016/j.ecolind.2014.08.033. [DOI] 🠔
  24. Sutherland DL, Turnbull MH, Craggs R. J. Environmental drivers that influence microalgal species in fullscale wastewater treatment high rate algal ponds. Water Res. 2017;124:504-512. Doi:10.1016/j.watres.2017.08.012. [DOI] 🠔
  25. Sardi-Saavedra A., Peña-Salamanca E, Madera-Parra C, Cerón-Hernández V. Diversidad de las comunidades de algas asociadas a un sistema algal de alta tasa fotosintética para la biorremediación de lixiviados de rellenos sanitarios. Lat Am J Aquat Res. 2016;44(1):113-120. Doi:10.3856/vol44-issue1-fulltext-11. [DOI] 🠔
  26. Tell G, Conforti V. Euglenophyta pigmentadas de la Argentina, Departamento de Ciencias Biológicas. Buenos Aires: Lubrecht & Cramer Ltd; 1986. 301 p. 🠔
  27. Valigore JM. Microbial (microalgal-bacterial) biomass grown on municipal wastewater for sustainable biofuel production. Christchurch: University of Canterbury; 2011. 164 p. 🠔
  28. Villafañe VE, Reid FM. Métodos de microscopía para la cuantificación del fitoplancton. In: Alveal K. et al ., editors. Manual de métodos ficológicos. Concepción: Universidad de Concepción; 1995. p. 169-185. 🠔
  29. Wehr J.D., Scheath R.G. Freshwater algae of North America, ecology and classification. 2nd ed. San Diego: Academic Press, an imprint of Elsevier Science; 2003.p.1-11. 🠔
  30. Wetzel R, Likens G. Limnological Analyses. 3rd ed. New York: Springer-Verlag; 2000. 429 p. 🠔
  31. XLSTAT. Software estadístico para Excel. Paris: Addinsoft. Available in: Available in: https://www.xlstat.com/es/ . [Cited 31 Jul 2018]. [URL] 🠔
  32. Zaixso H. Manual de campo para el muestreo de columna de agua, San Juan Bosco. 1st ed. Comodoro Rivadavia: Universidad Nacional de la Patagonia San Juan Bosco;2002. 191 p. 🠔
Sergi Sabater.
Sardi Saavedra A, Madera Parra C, Peña Salamanca EJ, Cerón VA, Mosquera J. Grupos funcionales fitoplanctónicos en una laguna algal de alta tasa usada para la biorremediación de lixiviados de rellenos sanitarios. Acta biol. Colomb. 2018;23(3):295-303. DOI: http://dx.doi.org/10.15446/abc.v23n3.69537
The authors declare that there is no conflict of interest.