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2021 Biodiversidad Macroinvertebrados en Chalhuanca Arequipa
2021 Biodiversidad Macroinvertebrados en Chalhuanca Arequipa
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Mary Carmen Quispe Mamani1*, Jose Francisco Villasante Benavides2, Daniel feriz García3, César R. Luque-
Fernández4, Anthony Pauca Tanco5 & Luis Nolberto Villegas Paredes6
1
Facultad de Ciencias Biológicas de la Universidad Nacional de San Agustín de Arequipa, Perú;
maquispema@unsa.edu.pe
2
Instituto de Investigación en Ciencia y Gestión Ambiental ICIGA, Universidad Nacional de San Agustín de Arequipa,
Perú; jvillasanteb@unsa.edu.pe
3
Unidad de investigación en Ecología Tropical-UNIET, Fundación Universitaria de Popayán, Colombia;
daniferiz@hotmail.com
4
Instituto de Investigación de Ciencia y Gestión Ambiental ICIGA, Universidad Nacional de San Agustín de Arequipa,
Perú; cluquef@unsa.edu.pe
5
Instituto de Investigación de Ciencia y Gestión Ambiental ICIGA, Universidad Nacional de San Agustín de Arequipa,
Perú; gpaucat@unsa.edu.pe
6
Sección de Ecología y Conservación, Facultad de Ciencias Biológicas, Universidad Nacional de San Agustín de
Arequipa, Perú; lvillegasp@unsa.edu.pe
*Corresponding author
ABSTRACT Water quality is an issue of global concern because of the evident contamination of the sources
of this resource. In recent decades the study of inland waters has been oriented towards the re-
covery and conservation of these ecosystems, in this sense abundant studies were carried out
in lotic systems, and to a lesser extent in lentic systems and in a much more reduced way in
high Andean wetlands. This work represents one of the few carried out in high Andean ecosys-
tems, and lentic such as are the Chalhuanca bofedales. The high Andean wetlands of Chal-
huanca provide important ecosystem services, among which stand out the water regulation,
water reservoirs, and endemic species habitats. The aim was to assess water quality in the high
Andean wetlands of Chalhuanca (Arequipa) using macroinvertebrate bioindicators. Samples
were taken during the wet season (January) and dry season (June) in 2018; 2 sampling methods
were used, Surber net for river and D-frame net for bofedal. Individuals were identified until
genus in most cases through taxonomic guides. Biotic quality was determined using the
BWMP/Bol, ABI and nPeBMWP indexes; physicochemical parameters were also evaluated
in each study site. We found 6 phylum, 10 classes, 18 orders, 26 families and 33 taxa. Accord-
ing to biotic index, sampling sites presented water quality from critical or bad to acceptable.
The physicochemical parameters were found in the range set by the ECAs of D.S.004-2017
MINAM, except the dissolved oxygen, which in the most study sites was lower than the es-
tablished for water intended for conservation of the aquatic environment. Regarding diversity,
it was found that it was greater in the dry season both in the river and in the bofedal, however,
the abundance varied, finding greater abundance in bofedales in the wet season and greater
abundance in the river in the dry season. The high Andean wetlands of Chalhuanca present a
limited diversity of macroinvertebrates families and a regular water quality in most sampling
sites.
and 2.12 °C. on dry season, with precipitation val- later processed in the laboratory. The physico-
ues of 476.12 mm on wet season and 8.74 mm on chemical parameters were recorded in situ prior
dry season (Ramos, 2018). Months of highest pre- to taking biological samples, always taking data
cipitation are from January to March, constituting in triplicate to minimize measurement error,
65% of the annual total; the relative humidity of the using a multiparametric sensor called Hanna
area does not exceed 50% (Coaguila et al., 2010). HI9829. The main variables measured were pH,
The plant composition is typical of a bofedal for this dissolved oxygen (DO), electrical conductivity
locality, where the most representative species are (EC), total dissolved solids (TDS) and tempera-
Distichia muscoides, Plantago rigida and Oxichloe ture (T°).
andina (Choque, 2017).
Sample processing
Sample design
Bofedal sample processing, the methodology
The selection of the sampling sites was made on recommended by Central Plains Center for
an area of 278 ha. A non-probabilistic sampling was BioAssessment (2005) was followed. The sample
used for convenience (Otzen & Manterola, 2017), from each bottle was homogenized, placed in a 30
establishing 8 sampling sites, 4 for the bofedales x 20 cm tray, a grid of 20 squares of equal dimension
and 4 for the Chalhuanca river (Table 1). Sampling was introduced; then a sub-sample of 4 squares cho-
was done during wet (January) and dry (June) sea- sen at random (20 % of the sample) was extracted.
sons of 2018. The subsamples were examined using a stereo mi-
croscope; the values obtained were extrapolated to
Macroinvertebrate sampling the total sample. Instead, river samples were re-
viewed in their entirety (100% of the sample).
About bofedales, the proposed methodology in For taxonomic identification of aquatic
the manual of collection methods for biological macroinvertebrates, the taxonomic keys of
communities was followed (Universidad Nacional Domínguez & Fernández (2009), Merritt et al.
Mayor de San Marcos & Museo de Historia Natu- (2008), Huamantinco & Ortiz (2010) and Thorp &
ral [UNMSM], 2014), where a D-net type network Covich (2015) were used, trying to classify the or-
with a mesh opening of 500 μm was used, with ganisms up to the most specific level possible.
two-meter sweep of the vegetation margin and an-
other sweep in the middle of the water body, repli- Data analysis
cations were made in underlying and similar water
bodies in the area. For the river habitat, a Surber Specific richness data were used, which is rep-
net (30 x 30 cm) with a mesh opening of 500 μm resented by the number of taxa found per sampling
was used, which was placed on the bottom and site. Abundance was determined as the number of
against the current, the replicas were separated by individuals per taxon found at each sampling site
a distance of 100 meters (UNMSM & Museo de
Historia Natural 2014). Sampling was always
started upstream.
A total of 45 samples in two seasons studied
were obtained, 24 samples in the river and 21 in
bofedales. From 24 river samples, 12 of them are
from wet season and 12 of them from dry season.
In bofedales, 21 samples were obtained, 12 from
wet season and 9 from dry season (it was not pos-
sible to take samples from the B2 site this year
because the water body suffered from drying out).
Each sample was stored in 500 ml plastic bottles
and preserved with 5% formaldehyde, recording Table 1. Geographical location of sampling sites in the
data on habitat, date of sampling, collector, and high Andean wetlands of Chalhuanca, Arequipa-Peru.
520 MARY CARMEN QUISPE MAMANI ET ALII
(Moreno, 2001). Diversity for each study season 31 on dry season. In bofedales 31 taxa were found
was calculated with the first order True Diversity and 29 taxa in the river. Regarding macroinverte-
index (1D) using the value of the Shannon-Wiener brates composition, 27 taxa were found to be shared
index with natural logarithm for transformation in both habitats, including Andesiops Lugo-Ortiz &
(Jost, 2006), because with this index the variation McCaffwerty, 1999, Hydroptila Dalman, 1819,
becomes more evident, since the results are given Cricotopus van der Wulp, 1874, Helobdella Blan-
in number of effective species, besides improving chard, 1896. Two taxa were presented exclusively
their understanding, since the number of effective for rivers, Muscidae and Claudioperla, and 4 genera
species allows the comparison of the magnitude of were presented exclusively for bofedales: Tropis-
the difference in diversity of two or more commu- termus Solier, 1834, Celina Aubé, 1837, Ischnura
nities (Moreno, 2001). The Dominance Index (D) Charpentier, 1840 and Atopsyche Banks, 1905.
and Pielou Equity (J') were determined (Moreno, In both seasons, the aquatic macroinvertebrate
2001), also the similarity index based on the Bray community was represented by the order Diptera
Curtis distance using the UPGMA linkage method with 5 families distributed in 10 taxa, followed by
(Moreno, 2001). To calculate those indexes we used the orders Coleoptera and Trichoptera with 3 fami-
statistical packages SPSS 25 and Past 3.25 (Ham- lies each of them (Table 2).
mer et al., 2001). The rank abundance curves (Fig. 1) show that
Finally, Mann-Whitney U test was applied to de- in the bofedal, on wet season, the genus Xiphimena
termine if there are differences in the abundance Cobb, 1913 is highly dominant followed by the
distribution between wet and dry seasons; the anal- family Lumbriculidae, while on dry season the
ysis was applied separately for each type of habitat Cyprididae and Xiphimena taxa were the most
(bofedales and river). abundant. Hydroptila and Hyalella S.I. Smith, 1874
appear in the river on wet season as the most abun-
Determination of water quality dant, while on dry season, Cricotopus sp. 1 and
Cricotopus sp. 2 are clearly the most abundant taxa,
Due to our study location, we used three in all cases the other taxa show similar abundances.
adapted indexes for ecosystems located at more In terms of richness, it was observed that all sea-
than 2,000 meters asl. These were BMWP/Bol sons presented greater richness on dry season, B3
(Ministerio del Medio Ambiente y Agua, 2011), site in bofedal and R4 site in river presented the
ABI (Acosta, Ríos, Rieradevall & Prat, 2009) and highest values of richness (Fig. 2).
nPeBMWP (Medina et al., 2010). Each sampling
site was categorized based on the sum of the scores Ecological Indexes
assigned for each index. The data of the physico-
chemical parameters obtained were evaluated for Comparing the diversity between seasons,
each season according to the national legal regula- whether in bofedal or river, true diversity index
tion of Peru, environmental quality standards shows the same pattern, more diversity on dry sea-
(ECA)-category 4: water destined to the conserva- son than on wet season. It is observed that bofedal
tion of the aquatic environment (MINAM, 2017). on dry season contains 2.36 times more effective
species than on wet season, while the river during
dry season contains 1.19 times more effective
RESULTS species than wet season (Table 3). In accordance
with these results, in both seasons and habitats,
Macroinvertebrate richness and diversity where diversity is higher so does equity and con-
versely so does dominance.
Abundance of Macroinvertebrates in the Chal- The Bray Curtis index associated two groups,
huanca wetlands was made up of 69,782 individuals with a cut-off line of 40% similarity, one group con-
for seasons and habitats evaluated, where it was sisting of the sites belonging to the bofedal and the
represented by six phylum, ten classes, 18 orders, other corresponding to study site on river, an ex-
26 families and 33 taxa (Table 2). For both habitats pected result due to the differences in types of habi-
a total of 29 taxa were recorded on wet season and tat (Fig. 3).
Diversity of aquatic macroinvertebrates and water quality of the High Andean wetlands of Chalhuanca, Arequipa-Peru 521
Physicochemical analysis
Figure 3. Bray-Curtis similarity dendrogram with the The greatest diversity was found on dry season,
UPGMA (linkage method) of the Chalhuanca wetland sam-
pling sites.
which coincides with the results found by Custodio
& Chanamé (2016) in the central highlands of Peru
at 3,440 meters asl, while in regards to the abun-
DISCUSSION dance, in bofedales it was greater in the wet season
and in the river it was greater in the dry season. This
The taxonomic richness found (28 families and variation in abundance in both ecosystems is due to
33 taxa) can be compared to high Andean environ- their typology, the bofedal being a lentic system and
ments above 3,000 meters, as both are similar (Ja- the river a lotic system. Giacometti & Bersosa
cobsen & Marín, 2008; Custodio & Chanamé, (2006) and Motta et al. (2017) mention that in river
2016), however, compared to lower altitude envi- the reduction of water that occurs in the dry season
ronments it is much lower (Meza, Días & Walteros, facilitates the establishment of macroinvertebrate
2012; Salcedo, Artica & Andrea., 2013). Jacobsen communities. This is because the drag of individu-
& Marín (2008) report a low richness of macroin- als caused by the rains is reduced, while in
vertebrates families above 4,000 meters asl as does bofedales the opposite occurs because the decrease
Acosta (2009) who describes that a greater number in the water in their water wells causes their desic-
of macroinvertebrates taxa prefer bodies of water cation, as well as the restriction of space and food
between 2,500 and 3,000 meters asl, so the altitude which leads to the decreased abundance.
at which Chalhuanca is located (4,338 meters asl) The Mann-Whitney U test in both types of habi-
could be a limitation for the settlement of macroin- tats, the bofedal and the river, showed that the dis-
vertebrates communities. tribution of abundances is not the same between the
However, Jacobsen & Marín (2008) explain that two seasons studied. In bofedales, this variation is
the low diversity in the Altiplano cannot be ex- evident by the greater dominance on wet season
plained only by the higher altitude, it is also due to compared to dry season, given the high abundance
the ecological conditions of the high Andean wet- of the family Longidoridae (phytoectoparasites
lands. In this sense, Toro et al. (2002) describe found in the soil). This family could have been
many causes of water quality degradation, such as dominant due to the dragging of sediments and the
contamination by organic matter, the presence of removal of soil by water runoff that occurs in the
persistent inorganic pollutants and anthropic inter- rainy season (Pérez et al., 2013).
vention, which were observed in the sampling sites This is supported by Flecker & Feifarek (1994)
being strong and permanent used in sheep grazing who mention that high levels of water in the rainy
524 MARY CARMEN QUISPE MAMANI ET ALII
Table 4. Water quality values for the biotic indexes: BMWP/Bol, ABI and nPeBMWP.
Table 5. Physical-chemical variables of the high Andean wetlands of Chalhuanca. W: wet season, D: dry season. (*)Values
below the permissible limit established in the national environmental water quality standards (ECA)s Supreme 2017
MINAM.
Diversity of aquatic macroinvertebrates and water quality of the High Andean wetlands of Chalhuanca, Arequipa-Peru 525
season condition a low density in macroinvertebrate inciding with the study of Meza et al. (2012) in the
communities and low levels corresponding to the upper sub-basin of the Chinchiná River.
dry season allow the recovery of macroinvertebrate According to Rivera (2004) the concentration of
communities; and coincides with the findings of dissolved oxygen is generally high and constant in
Molina et al. (2008) in their study carried out in a Andean rivers, so this is not usually a limiting fac-
high Andean river in the Royal Mountain Range of tor. However, in the high Andean wetlands of Chal-
Bolivia. huanca, most of the study sites (73%) presented
Family Gripopterygidae is only in the river is values that were lower than those required for the
due to its low temperature requirements, presence category destined to the conservation of the aquatic
of fallen stones or branches and areas with a good environment, established in the ECAs for Peru -
state of conservation (Domínguez & Fernández, 2017 (MINAM, 2017).
2009). This family was recorded at R4 and R2 sites, The low concentration of dissolved oxygen
which had the above-mentioned characteristics, but could be related to the accumulation of sheep faecal
with very few individuals, a result that could be re- remains, since dissolved oxygen is strongly related
lated to habitat alteration by pollution. to the concentration of organic matter according to
Family Dytiscidae is an exclusive family for Forero (2017).
bofedales, which is generally found in lentic envi- In conclusion, the high Andean wetland of
ronments, and in lotic water bodies they are more Chalhuanca presents a limited diversity of
frequently observed in backwaters, where current macroinvertebrates families, regular water quality
velocity is low or null (Domínguez & Fernández, above the BMWP, nPeBMWP and ABI indexes,
2009), these conditions may have limited the pres- and is home to a low fluvial fauna composed of
ence of this family to bofedales. aquatic organisms, which should be given greater
Some organisms such as Cricotopus, Andesiops, attention as indicators of the ecological state of
and Hydroptila were found in all eight sites, be- these ecosystems. It is recommended to perform
cause they are organisms that occupy a wide spec- monthly studies throughout all climatic periods, for
trum of environmental conditions, (eurithophics) a better understanding of the functioning of the
(Domínguez & Fernández, 2009; Acosta, 2009). community structure of aquatic macroinvertebrates
of Chalhuanca. In addition, it is suggested that pol-
Water Quality lution tolerance studies be conducted on the fami-
lies Limnesiidae and Limnozetidae of the class
According to the results of the BMWP/Bol, ABI Arachnida, for which no scores were found in the
and nPeBMWP indexes 77.78 % of the study sites index used, making an accurate evaluation of the
have water of doubtful or regular quality. Compar- ecological status difficult.
ing both seasons with the BMWP index, the water
quality in most of them was the same, this coincides
with the study carried out by Zamora et al. (1995) ACKNOWLEDGEMENTS
in the Genil basin, finding that there was no vari-
ability between the different seasons of the year, de- We thank the Universidad Nacional de San Agustín
spite the fact that a common criticism is that the use de Arequipa, for the financing of this work, accord-
of biotic indexes shows a dependency related to the ing to grant contract TP-12-2018. We would also
seasons of the year. like to thank the laboratory of the Ecology and Con-
Authors such as Toro et al. (2002) and Mancilla servation section of the Universidad Nacional de
et al. (2009) refer to the influence of physicochem- San Agustín de Arequipa (Peru), the Ecology labo-
ical factors on the aquatic macroinvertebrates com- ratory of the Fundación Universitaria de Popayán
munity, emphasizing that water temperature and (Colombia) and the research project “Servicios eco-
oxygen availability are determining factors in the sistémicos de los humedales altoandinos y su con-
distribution of these organisms. In our study we tribución en la mitigación de los efectos del cambio
found greater richness on dry season which pre- climático: estudio de caso (IBA-047-2016-UNSA),
sented a higher concentration of dissolved oxygen for providing the space and equipment for the de-
and lower temperature compared to wet season, co- velopment of this study.
526 MARY CARMEN QUISPE MAMANI ET ALII
macroinvertebrados bentónicos en arroyos de climas Moreno C., 2001. Métodos para medir la biodiversidad.
templados, Chile central. Hidrobiología, 19: 193– En: CYTED, ORCYT - UNESCO y SEA (Eds.),
203. http://www.scielo.org.mx/scielo.php?script= M&T-Manuales y Tesis SEA,Vol. 1 (pp. 84).
sci_arttext&pid=S0188-88972009000300002 Zaragoza, España: ORCYT/UNESCO & SEA.
Mango B., 2017. Valoración económica de los servicios Motta A., Longo M., & Aranguren N., 2017. Variación
ecosistemáticos de la regulación de los bofedales del temporal de la diversidad taxonómica y rasgos fun-
centro poblado de Chalhuanca, distrito de Yanque, cionales de los macroinvertebrados acuáticos en ríos
provincia de Caylloma, región Arequipa (Tesis de temporales en la isla de Providencia, Colombia. Acta
pregrado). Universidad Nacional de San Agustín. Biológica Colombiana, 39 (107): 82–100.
Arequipa, Perú. https://doi.org/10.17533/udea.acbi.v39n107a10
Medina C., Hora M., Ascencio I., Pereda W. & Gabriel Otzen T. & Manterola C., 2017. Técnicas de Muestreo
R., 2010. El índice Biological Monitoring Working sobre una Población a Estudio. International Journal
Party (BMWP), modificado y adaptado a tres mi- of Morphology, 35: 227–232. https://scielo.conicyt.
crocuencas del Alto Chicana. La Libertad, Perú. cl/scielo.php?pid=S0717-95022017000100037&
2008. Uniciencia, 1: 5–20. http://revistas.unitru. script=sci_abstract
edu.pe/index.php/SCIENDO/article/view/280 Pérez A., Benetti C. & Garrido J., 2013. Estudio de la
Merritt R., Cummins K. & Berg M. (Eds.), 2008. An in- calidad del agua del río Furnia mediante el usos de
troduction to the aquatic insects of North America, macroinvertebrados acuáticos. Nova Acta Científica
4th edition. Iowa, Kendall Hunt Publishing, 1158 Compostelana (Bioloxía), 20: 1–9. https://pdfs.se-
pp. manticscholar.org/c03e/b18a48795c8229eca9aab190
Meza A., Días L. & Walteros J., 2012. Calidad de agua y 41670bad9bd5.pdf
composición de macroinvertebrados acuáticos en la Quintero M. (Ed.), 2010. Servicios ambientales
subcuenca alta del río Chinchiná. Caldasia, 34: 443– hidrológicos en la región andina. Estado del
456. https://revistas.unal.edu.co/index.php/cal/arti- conocimiento, la acción y la política para asegurar su
cle/view/39163/46608 provisión mediante esquemas de pago por servicios
Ministerio del Ambiente del Perú, 2010. Compendio de ambientales. Lima, Perú: CONDESAN.
la legislación ambiental peruana. Política e instru- Ramos C., 2018. Variación espacio-temporal de los eco-
mentos de gestión ambiental (Vol. 3). Recovered sistemas de humedales altoandinos en el anexo de
from https://sinia.minam.gob.pe/documentos/com- Chalhuanca del distrito de Yanque (Caylloma, Are-
pendio-legislacion-ambiental-peruana-vol-iii-polit- quipa) entre los años 1986–2016 (Tesis de pregrado).
ica-instrumentos Universidad Nacional de San Agustín. Arequipa,
Ministerio del Medio Ambiente y Agua, 2011. Guía para Perú.
la evaluación de las condiciones biológicas de cuer- Rivera R., 2004. Estructura y composición de la comu-
pos de agua utilizando macroinvertebrados bentóni- nidad de macroinvertebrados bentónicos en ríos de
cos. Estado Plurinacional de Bolivia. páramo y zonas boscosas, en los andes venezolanos
http://jcmendo.com/wp-content/uploads/2018/docs- (Tesis de pregrado). Universidad de los Andes,
publi-cursos/documentacion-tecnica/Guia%20de%20 Mérida, Venezuela.
Evalaucion%20de%20Condiciones%20Biologicas% Roldán G., 1992. Fundamentos de Limnología Neotro-
20MMAYA.pdf ropical. Medellín, Colombia: Universidad de Antio-
Ministerio del Ambiente, 2017. Decreto Supremo N° quia, Medellín.
004-2017. Aprueban Estándares de Calidad Ambien- Rosas J., Ávila H., Sánchez A., Rosas A., García S.,
tal (ECA) para Agua y establecen Disposiciones Sampedro L., Granados J. & Juárez A., 2014. Índice
Complementarias. https://sinia.minam.gob.pe/nor- BMWP, FBI y EPT para determinar la calidad del agua
mas/aprueban-estandares-calidad-ambiental-eca- en la laguna de Coyuca de Benítez, Guerrero, México.
agua-establecen-disposiciones Revista Iberoaméricana de Ciencias, 1: 81–88.
Ministerio del Ambiente, 2019. Mapa Nacional de Eco- http://reibci.org/publicados/2014/julio/2200103. pdf
sistemas del Perú, Memoria Descriptiva. https://cdn. Salcedo S., Artica L. & Andrea F., 2013. Universidad
www.gob.pe/uploads/document/file/309735/Memo- Continental. Macroinvertebrados bentónicos como
ria_descriptiva_mapa_Nacional_de_Ecosistemas.pdf indicadores de la calidad de agua en la microcuenca
Molina C., Gibon F., Pinto J. & Rosales C., 2008. Estruc- San Alberto, Oxapampa, Perú. Apuntes de Ciencia y
tura de macroinvertebrados acuáticos en un río Al- Sociedad, 3: 2. http://journals.continental.edu.pe/
toandino de la Cordillera Real, Bolivia: variación index.php/apuntes/article/view/197/195
anual y longitudinal en relación a factores ambien- Thorp J. & Rogers D. (Eds.), 2015. Thorp and Covich‘s
tales. Ecología aplicada, 7: 105–116. http://www.sci- freshwater invertebrates. Ecology and general biol-
elo.org.pe/pdf/ecol/v7n1-2/a13v7n1-2.pdf ogy, 1, 4th edn. London, Francia: Academic Press.
528 MARY CARMEN QUISPE MAMANI ET ALII
Toro M., Robles S., Avilés J., Nuño C., Vivas S., Bonada necton (peces) en aguas continentales del Perú.
N., Prat N., Alba J., Casas J., Guerrero C., Jáimez P., http://www.minam.gob.pe/diversidadbiologica/wp-
Moreno J., Moyá G., Ramon G., Suárez M., Vidal M., content/uploads/sites/21/2014/02/M%C3%A9todos-
Álvarez M. & Pardo I., 2002. Calidad de las aguas de de-Colecta-identificaci%C3%B3n-y-an%C3%A1lisi
los ríos mediterráneos del proyecto GUADALMED, s-de-comunidades-biol%C3%B3gicas.compressed.
características físico-químicas. Limnetica, 21: 63–75. pdf
https://www.limnetica.com/documentos/limnetica/li Zamora C., Sáinz C., Sánchez A. & Alba J., 1995. Are
mnetica-21-2-p-63.pdf biological índices BMWP’ and ASPT’ and their sig-
Universidad Nacional Mayor de San Marcos & Museo nificance regarding water quality seasonally depen-
de Historia Natural, 2014. Métodos de colecta, iden- dent? Factors explaining their variations. Water
tificación y análisis de comunidades biológicas: Research, 29: 285–290. http://hera.ugr.es/doi/1500
plancton, perifiton, bentos (macroinvertebrados) y 4338.pdf