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Fish functional groups in a tropical wetland of the Yucatan Peninsula, Mexico

ABSTRACT

The characterization of species' functional traits is a major step in the understanding and description of communities in natural habitats. The classification of species into functional groups is a useful tool to identify redundancy and uniqueness. We studied the fish community of a pristine freshwater wetland in the Sian Ka'an Biosphere Reserve by analysing two multidimensional functions: food acquisition and locomotion. We investigated changes in the functional group structure between habitats (permanent and temporary pools) and seasons (dry and wet). Six functional groups with different ecological characteristics were detected, two of which had high functional redundancy and three of them were represented by single species with unique ecological functions. In permanent pools during the dry season, functional group richness and diversity were lower, while evenness was higher. During the wet season, all functional groups were detected and similar functional group structure was found between habitats. These results suggest an effect of environmental filtering during the dry season and niche complementarity during the wet season.

Keywords:
Community ecology; Environmental filtering; Functional groups; Functional redundancy; Freshwater wetland

RESUMEN

La caracterización de los rasgos funcionales de las especies es un paso importante en la comprensión y descripción de las comunidades en hábitats naturales. La clasificación de especies en grupos funcionales es una herramienta útil para identificar la redundancia y la especialización. Se estudió la comunidad de peces de un humedal prístino de agua dulce en la Reserva de la Biosfera de Sian Ka'an, analizando dos funciones multidimensionales: adquisición de alimento y la locomoción. Analizamos los cambios en la estructura de los grupos funcional entre hábitats (permanentes y temporales) y temporadas (lluvias y secas). Seis grupos funcionales con características ecológicas distintas fueron detectados, dos de los cuales presentaron una alta redundancia funcional y tres de ellos están representados únicamente por una especie con una función ecológica particular. En las pozas permanentes durante la temporada de secas, la riqueza y diversidad de grupos funcionales fueron menores; mientras que la equitatividad de grupos funcionales fue mayor. Durante la temporada de lluvias se detectaron todos los grupos funcionales y la estructura de los grupos fue similar entre los hábitat. Estos resultados sugieren que los filtros ambientales tienen un efecto durante la temporada de secas y la complementariedad de nicho durante la temporada de lluvias.

Introduction

Classical approaches to understand changes in diversity are based on the analysis of species richness, abundance, and diversity/evenness indices (Morin, 2011Morin, P. J. (Ed.). 2011. Community ecology. Oxford, Wiley Blackwell, 424p.). However, describing communities using traditional diversity measures ignores among-taxa differences in ecological function (Chave, 2004Chave, J. 2004. Neutral theory and community ecology. Ecology Letters, 7: 241-253.; Villéger et al., 2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.). Recently, the study of functional diversity has emerged with the objective of incorporating specific attributes of species into the analysis of changes in taxonomic diversity (Tilman et al., 1997Tilman, D., J. Knops, D. Wedin, P. Reich, M. Ritchie & E. Siemann. 1997. The influence of functional diversity and composition on ecosystem processes. Science, 277: 1300-1302.; Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.; Scherer-Lorenzen, 2005Scherer-Lorenzen, M. 2005. Biodiversity and ecosystem functioning: basic principles. In: Barthlott, W., E. Linsenmair & S. Porembski (Eds.). Biodiversity: Structure and Function. Oxford, EOLSS Publishers.; Cadotte et al., 2011Cadotte, M. W., K. Carscadden & N. Mirotchnick. 2011. Beyond species: functional diversity and the maintenance of ecological processes and services. Journal of Applied Ecology, 48: 1079-1087.). Furthermore, functional diversity has been proposed as a useful framework for the understanding of relations among diversity, community structure and ecosystem functioning (Díaz & Cabido, 2001Díaz, S. & M. Cabido. 2001. Vive la différence: plant functional diversity matters to ecosystem processes. Trends in Ecology & Evolution, 16: 646-655.; Naeem & Wright, 2003Naeem, S. & J. P. Wright. 2003. Disentangling biodiversity effects on ecosystem functioning: deriving solutions to a seemingly insurmountable problem. Ecology Letters, 6: 567-579.).

Functional niche and functional redundancy are two main concepts of functional diversity. A functional niche is analogous to an ecological niche and represents a n-dimensional hypervolume in a functional space, where the axes represent the key functions associated with different functional traits (Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.). Functional traits are those biological traits that influence the performance of organisms (Hooper et al., 2005Hooper, D. U., F. S. Chapin III, J. J. Ewel, A. Hector, P. Inchausti, S. Lavorel, J. H. Lawton, D. M. Lodge, M. Loreau, S. Naeem, B. Schmid, H. Setälä, A. J. Symstad, J. Vandermeer & D. A. Wardle. 2005. Effects of biodiversity on ecosystem functioning: a consensus of current knowledge. Ecological Monographs, 75: 3-35.; Villéger et al., 2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.) and that may be related to ecosystem processes (flow of energy and matter), ecosystem stability (resistance and resilience), biological interactions (intra- and interspecific), and habitat modification. In turn, functional redundancy is based on the idea that some species may play similar roles in communities and ecosystems (i.e. , similar functional niches). Therefore, the loss of a redundant species in a local community is likely to have a smaller impact on ecosystem processes because other species share its functional niche (Lawton & Brown, 1994Lawton, J. H. & V. K. Brown. 1994. Redundancy in ecosystems. Pp. 255-270. In: Schulze, E. D. & H. A. Mooney (Eds.). Biodiversity and ecosystem function. Berlin, Springer, 525p.; Fonseca & Ganade, 2001Fonseca, C. R. & G. Ganade. 2001. Species functional redundancy, random extinctions and the stability of ecosystems. Journal of Ecology, 89: 118-125.).

One way to assess the functional redundancy among species within a community is based on the classification of species into functional groups (Dumay et al., 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.), which consists in conforming discrete sets of species according to the similarity of their functional traits (Tilman, 2001Tilman, D. 2001. Functional diversity. In: Levin, S. A. (Ed.). Encyclopedia of Biodiversity. San Diego, Academic Press.). Some limitations have been recognized for this method as it depends on the functional traits that are selected for analysis, it cannot detect ontogenetic changes in function, it is not sensitive to changes in feeding ecology and habitat use during the life cycle, and it assumes that the interspecific variation exceeds intraspecific variation (Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.; Hubbell, 2005Hubbell, S. P. 2005. Neutral theory in community ecology and the hypothesis of functional equivalence. Functional Ecology, 19: 166-172.; Hoeinghaus et al., 2007Hoeinghaus, D. J., K. O. Winemiller & J. S. Birnbaum. 2007. Local and regional determinants of stream fish assemblages structure: inferences based on taxonomic vs. functional groups. Journal of Biogeography, 34: 324-338.). Yet, this method presents important advantages: it is flexible rather than arbitrary because functional traits can be added exhaustively (Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.), taxonomic similarity is not a prerequisite for the existence of functional similarity (Morin, 2011Morin, P. J. (Ed.). 2011. Community ecology. Oxford, Wiley Blackwell, 424p.), and its construction in a given community can be achieved with a relatively small investment of time (Fonseca & Ganade, 2001Fonseca, C. R. & G. Ganade. 2001. Species functional redundancy, random extinctions and the stability of ecosystems. Journal of Ecology, 89: 118-125.; Dumay et al. , 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.). Previous studies have shown that the effect of functional groups on ecosystem processes is greater than that of species richness (Tilman et al. , 1997Tilman, D., J. Knops, D. Wedin, P. Reich, M. Ritchie & E. Siemann. 1997. The influence of functional diversity and composition on ecosystem processes. Science, 277: 1300-1302.; Scherer-Lorenzen, 2005Scherer-Lorenzen, M. 2005. Biodiversity and ecosystem functioning: basic principles. In: Barthlott, W., E. Linsenmair & S. Porembski (Eds.). Biodiversity: Structure and Function. Oxford, EOLSS Publishers.; Srivastava & Vellend, 2005Srivastava, D. S. & M. Vellend. 2005. Biodiversity-ecosystem function research: is it relevant to conservation?. Annual Review of Ecology, Evolution and Systematics, 36: 267-294.; Balvanera et al., 2006Balvanera, P., A. B. Pfisterer, N. Buchmann, J. S. He, T. Nakashizuka, D. Raffaelli & B. Schmid. 2006. Quantifying the evidence for biodiversity effects on ecosystem functioning and services. Ecology Letters, 9: 1146-1156.). Also, this method has been useful to understand assembly patterns of communities (Brown et al., 2000Brown, J. H., B. J. Fox & D. A. Kelt. 2000. Assembly rules: desert rodent communities are structured at scales from local to continental. The American Naturalist, 156: 314-321.; Bellwood et al., 2002Bellwood, D. R., P. C. Wainwright, C. J. Fulton & A. Hoey. 2002. Assembly rules and functional groups at global biogeographical scales. Functional Ecology, 16: 557-562.; Hoeinghaus et al. , 2007Hoeinghaus, D. J., K. O. Winemiller & J. S. Birnbaum. 2007. Local and regional determinants of stream fish assemblages structure: inferences based on taxonomic vs. functional groups. Journal of Biogeography, 34: 324-338.), to analyse the effect of species loss on ecosystem functioning (Naeem, 2002Naeem, S. 2002. Ecosystem consequences of biodiversity loss: the evolution of a paradigm. Ecology, 83: 1537-1552.), and to identify functional equivalences among species (Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.; Dumay et al. , 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.).

Fish communities represent an excellent model to investigate functional diversity with different trophic levels in natural environments (Duffy, 2002Duffy, J. E. 2002. Biodiversity and ecosystem function: the consumer connection. Oikos, 99: 201-219.; Córdova-Tapia & Zambrano, 2015Córdova-Tapia, F. & L. Zambrano. 2015. La diversidad funcional en la ecología de comunidades. Ecosistemas, 24: 78-87.). Studies of functional groups in fish communities have shown highly congruent patterns of habitat use, assemblage structure and functional redundancy at global biogeographic (Bellwood et al., 2002Bellwood, D. R., P. C. Wainwright, C. J. Fulton & A. Hoey. 2002. Assembly rules and functional groups at global biogeographical scales. Functional Ecology, 16: 557-562.), regional (Aguilar-Medrano & Calderon-Aguilera, 2015Aguilar-Medrano, R. & Calderon-Aguilera L. E. 2015. Redundancy and diversity of functional reef fish groups of the Mexican Eastern Pacific. Marine Ecology, 37: 119-133.), and local scales (Hoeinghaus et al., 2007Hoeinghaus, D. J., K. O. Winemiller & J. S. Birnbaum. 2007. Local and regional determinants of stream fish assemblages structure: inferences based on taxonomic vs. functional groups. Journal of Biogeography, 34: 324-338.; Teresa & Casatti, 2012Teresa, F. B. & L. Casatti. 2012. Influence of forest cover and mesohabitat types on functional and taxonomic diversity of fish communities in Neotropical lowland streams. Ecology of Freshwater Fish, 21: 433-442.; Bordignon et al., 2015Bordignon, C. R., L. Casatti, M. A. Pérez-Mayorga, F. B. Teresa & G. L. Brejão. 2015. Fish complementarity is associated to forests in Amazonian streams. Neotropical Ichthyology, 13: 579-590.). A useful tool to understand the ecological function of fish consists in the analysis of functional traits by means of an ecomorphological approach (Mason et al., 2007Mason, N. W. H., C. Lanoiselée, D. Mouillot, P. Irz & C. Argillier. 2007. Functional characters combined with null models reveal inconsistency in mechanisms of species turnover in lacustrine fish communities. Oecologia, 153: 441-452.; Mouillot et al., 2006Mouillot, D., O. Dumay & J. A. Tomasini. 2006. Limiting similarity, niche filtering and functional diversity in coastal lagoon fish communities. Estuarine, Coastal and Shelf Science, 71: 443-456.; Villéger et al., 2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.; Mouchet et al., 2013Mouchet, M. A., M. D. M. Burns, A. M. Garcia, J. P. Vieira & D. Mouillot. 2013. Invariant scaling relationship between functional dissimilarity and co-occurrence in fish assemblages of the Patos Lagoon estuary (Brazil): environmental filtering consistently overshadows competitive exclusion. Oikos, 122: 247-257.). Two key functions have been recognized: locomotion and food acquisition. Locomotion is related to fish swimming behaviour and habitat use, whereas food acquisition describes the trophic position and foraging behaviour in the water column (Dumay et al., 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.; Boyle & Horn, 2006Boyle, K. S. & M. H. Horn. 2006. Comparison of feeding guild structure and ecomorphology of intertidal fish assemblages from central California and central Chile. Marine Ecology Progress Series, 319: 65-84.; Villéger et al. , 2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.).

The Sian Ka'an Biosphere Reserve (SKBR) is located on the east coast of the Yucatan Peninsula, Mexico. It provides a unique opportunity for the study of the structure and drivers of fish communities in a freshwater wetland that lacks anthropogenic alterations (Zambrano et al., 2006Zambrano, L., E. Vázquez-Domínguez, D. García-Bedoya, W. F. Loftus & J. C. Trexler. 2006. Fish community structure in freshwater karstic water bodies of the Sian Ka'an Reserve in the Yucatan peninsula, Mexico. Ichthyological Exploration of Freshwaters, 17: 193-206.). These wetlands have a clear seasonal hydroperiod (wet and dry seasons), therefore fish communities experience habitat contractions and a high mortality rate during the dry season (Loftus & Kushlan, 1987Loftus, W. F. & J. A. Kushlan. 1987. Freshwater fishes of southern Florida. Bulletin of the Florida State Museum, Biological Sciences, 31: 147-344.; Trexler et al., 2005Trexler, J. C., W. F. Loftus & S. Perry. 2005. Disturbance frequency and community structure in a twenty-five year intervention study. Oecologia, 145: 140-152.). In SKBR, wetlands are constituted by permanent and temporary pools and their connection depend on hydro-meteorological conditions (Zambrano et al. , 2006Zambrano, L., E. Vázquez-Domínguez, D. García-Bedoya, W. F. Loftus & J. C. Trexler. 2006. Fish community structure in freshwater karstic water bodies of the Sian Ka'an Reserve in the Yucatan peninsula, Mexico. Ichthyological Exploration of Freshwaters, 17: 193-206.). During the wet season, flood allows fish dispersion and colonization of new habitats (Escalera-Vázquez & Zambrano, 2010Escalera-Vázquez, L. H. & L. Zambrano. 2010. The effect of seasonal variation in abiotic factors on fish community structure in temporary and permanent pools in a tropical wetland. Freshwater Biology, 55: 2557-2569.). During the dry season, some temporary pools completely dry-out depending on the duration and severity of the season. In contrast, permanent pools are always connected to the groundwater system and serve as refuges for fish. The dynamic of this annual system provides an excellent model to test how habitat contraction/expansion changes the functional structure of fish assemblages.

In this study, we characterized the fish community by analysing two multidimensional functions, namely food acquisition and locomotion, to: i) determine functional redundancy by defining functional groups, and to ii) evaluate changes in the functional group structure between habitats (permanent and temporary pools) and seasons (dry and wet). Our hypothesis is that, during the dry season, environmental filters change functional groups structure due to harsh conditions. These changes are likely related to food availability and water column height, which affect the survival of each species according to their ecological functions.

Material and Methods

Study site. The Sian Ka'an Biosphere Reserve (SKBR, 5281 km2) is located on the east coast of the Yucatan Peninsula, Mexico, a calcareous low plateau (Fig. 1). Approximately 30% of its total area consists of wetlands with a clear hydroperiod marked by a wet (May to February) and dry season (March and April) (Gondwe et al., 2010Gondwe, B. R. N., S. H. Hong, S. Wdowinski & P. Bauer-Gottwein. 2010. Hydrologic dynamics of the ground-water-dependent Sian Ka'an wetlands, Mexico, derived from InSAR and SAR data. Wetlands, 30: 1-13.; Escalera-Vázquez & Zambrano, 2010Escalera-Vázquez, L. H. & L. Zambrano. 2010. The effect of seasonal variation in abiotic factors on fish community structure in temporary and permanent pools in a tropical wetland. Freshwater Biology, 55: 2557-2569.), with an annual rainfall of 1,898.5 mm (CONAGUA, 2013CONAGUA, 2013. Reporte del Clima en México. Servicio Meteorológico Nacional. México, 23p.). During the wet season, storms help to interconnect wetlands, freshwater swamp forests and a variety of freshwater systems. These wetlands are relatively free from anthropogenic alterations (i.e. , non-native species and land-use change), leaving the hydrological regime unmodified (Zambrano et al. , 2006Zambrano, L., E. Vázquez-Domínguez, D. García-Bedoya, W. F. Loftus & J. C. Trexler. 2006. Fish community structure in freshwater karstic water bodies of the Sian Ka'an Reserve in the Yucatan peninsula, Mexico. Ichthyological Exploration of Freshwaters, 17: 193-206.).

Fig. 1
Geographic location of the study site (white star) in Sian Ka'an Biosphere Reserve, Mexico.

Our study was carried out in 11 pools within a continuous freshwater wetland (~5 km2; 19°48'27.11"N, 87°40'58.17"W) covered with periphyton mats (Zambrano et al., 2006Zambrano, L., E. Vázquez-Domínguez, D. García-Bedoya, W. F. Loftus & J. C. Trexler. 2006. Fish community structure in freshwater karstic water bodies of the Sian Ka'an Reserve in the Yucatan peninsula, Mexico. Ichthyological Exploration of Freshwaters, 17: 193-206.) and a flooded dense matrix of sawgrass (Cladium jamaicense Crantz, 1766), gulf-coast spikerush (Eleocharis cellulosa Torrey, 1836), and cattail (Typha domingensis Persoon, 1807) (Escalera-Vázquez & Zambrano, 2010Escalera-Vázquez, L. H. & L. Zambrano. 2010. The effect of seasonal variation in abiotic factors on fish community structure in temporary and permanent pools in a tropical wetland. Freshwater Biology, 55: 2557-2569.). In this wetland, there are small permanent pools (~3 m2 and ~50 cm deep) called 'petenes', which are surrounded by islands that are populated mainly by palm tree (Acoelorrhaphe wrightii Grisebach and Wendland, 1907). In this wetland, we sampled six permanent pools along with five temporary pools that were spatially close and that had at least 40 cm deep; the mean distance between pools was 75 m. At the beginning of the wet season habitats expand but permanent and temporary pools may remain isolated until the maximum water level is reached (August-September), which depends on the rainfall pattern.

Fish sampling. Sampling took place at the end of the dry season (April 2013) and at the maximum water level in the wet season (September 2013). Fish sampling was performed using un-baited Gee's minnow traps set for 24 hours (42 cm, 2 mm mesh and a funnel-entrance diameter of 3 and 4 cm), and repeated for three consecutive days in each pool and season. Due to differences in pool sizes between habitats and seasons, six traps were set in permanent pools during the dry season and eight during the wet season; for temporary pools, eight and ten traps were set, respectively. To standardized data, catch per unit effort was used (CPUE; total biomass/ number of traps) and relative biomass abundance was calculated. In each pool, half of the traps were placed along near-shore macrophytes and half in open water; they were placed partially submerged to avoid fish mortality due to low oxygen concentrations during the night. After each 24-hour period, individuals were collected and identified according to Schmitter-Soto (1998Schmitter-Soto, J. J. (Ed.). 1998. Catálogo de los peces continentales de Quintana Roo. San Cristóbal de las Casas, ECOSUR, 239p.), measured, weighed and then released in situ . Due to the small size of pools (~3 m2 in area and ~50 cm deep) this method has proved to be efficient and robust to sample fish in this system (Zambrano et al., 2006Zambrano, L., E. Vázquez-Domínguez, D. García-Bedoya, W. F. Loftus & J. C. Trexler. 2006. Fish community structure in freshwater karstic water bodies of the Sian Ka'an Reserve in the Yucatan peninsula, Mexico. Ichthyological Exploration of Freshwaters, 17: 193-206.; Escalera-Vázquez & Zambrano, 2010Escalera-Vázquez, L. H. & L. Zambrano. 2010. The effect of seasonal variation in abiotic factors on fish community structure in temporary and permanent pools in a tropical wetland. Freshwater Biology, 55: 2557-2569.). Furthermore, in this wetland, most of the fish species are relatively short-lived and do not reach large sizes (< 10 cm total length); all species recorded in the system have been caught using this method. Voucher specimens were deposited at the Colección Nacional de Peces, Instituto de Biología, Universidad Nacional Autónoma de México (Table 1).

Table 1
List of species and principal food items. *Based on: Soto-Galera (2006Soto-Galera, E. 2006. Ictiofauna de los corredores biológicos Sierra Madre del Sur y Selva Maya Zoque. Comisión Nacional para el Conocimiento y Uso de la Biodiversidad, Y026.); Miller (2009Miller, R. R. (Ed.). 2009. Peces dulceacuícolas de México. Ciudad de México, Comisión Nacional para el Conocimiento y Uso de la Biodiversidad, 559p.); Schmitter-Soto et al. (2011Schmitter-Soto, J. J., L. E. Ruiz-Cauich, R. L. Herrera & D. González-Solís. 2011. An index of biotic integrity for shallow streams of the Hondo River basin, Yucatan Peninsula. Science of the Total Environment, 409: 844-852.); Hinojosa-Garro et al. (2013Hinojosa-Garro, D., J. Arceo-Gómez, L. Zambrano & L. H. Escalera-Vázquez. 2013. Fish diet composition in permanent and semi-permanent pools in tropical wetlands of the Yucatan Peninsula. Neotropical Ichthyology, 11: 881-890.).

Functional characterization. In order to reduce the effect of fish removal on community structure analysis, the functional characterization was performed with individuals captured during an additional sampling period at the end of the dry season (May 2013). Fish sampling was performed in other pools using 25 un-baited minnow traps set for 24 hours for five consecutive days. Functional characterization was performed on a maximum of 15 adult individuals randomly selected from each species (Table 1). In the laboratory, fish were anesthetized with benzocaine (250 mg/L) before they were euthanized by overdose (Hinojosa-Garro et al., 2013Hinojosa-Garro, D., J. Arceo-Gómez, L. Zambrano & L. H. Escalera-Vázquez. 2013. Fish diet composition in permanent and semi-permanent pools in tropical wetlands of the Yucatan Peninsula. Neotropical Ichthyology, 11: 881-890.). Immediately, mouth traits were measured and high-quality photographs were taken. Later, we measured additional morphological measurements that require dissection (gut length and length of the longest gill raker), and photographs were analysed using ImageJ Software (U.S.-NIH). The functional characterization of fish species was based on the method proposed by Villéger et al. (2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.) using two key functions: food acquisition and locomotion. Food acquisition considers functional traits related to the size of food items, feeding method in the water column, filtering ability, prey detection and trophic position (Kramer & Bryant, 1995Kramer, D. L. & M. J. Bryant. 1995. Intestine length in the fishes of a tropical stream: 2. Relationships to diet - the long and short of a convoluted issue. Environmental Biology of Fishes, 42: 129-141.; Sibbing & Nagelkerke, 2001Sibbing, F. A. & L. A. J. Nagelkerke. 2001. Resource partitioning by Lake Tana barbs predicted from fish morphometrics and prey characteristics. Reviews in Fish Biology and Fisheries, 10: 393-437.; Karpouzi & Stergiou, 2003Karpouzi, V. S. & K. I. Stergiou. 2003. The relationships between mouth size and shape and body length for 18 species of marine fishes and their trophic implications. Journal of Fish Biology, 62: 1353-1365.; Boyle & Horn, 2006Boyle, K. S. & M. H. Horn. 2006. Comparison of feeding guild structure and ecomorphology of intertidal fish assemblages from central California and central Chile. Marine Ecology Progress Series, 319: 65-84.; Villéger et al. , 2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.). Likewise, locomotion is a measure related to habitat use, vertical position in the water column, hydrodynamism, fin use for manoeuvrability, and propulsion and acceleration efficiency (Webb, 1984Webb, P. W. 1984. Form and function in fish swimming. Scientific American, 251: 72-82.; Sibbing & Nagelkerke, 2001Sibbing, F. A. & L. A. J. Nagelkerke. 2001. Resource partitioning by Lake Tana barbs predicted from fish morphometrics and prey characteristics. Reviews in Fish Biology and Fisheries, 10: 393-437.; Dumay et al., 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.; Fulton et al., 2001Fulton, C. J., D. R. Bellwood & P. C. Wainwright. 2001. The relationship between swimming ability and habitat use in wrasses (Labridae). Marine Biology, 139: 25-33.; Villéger et al. , 2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.).

For food acquisition, 10 morphological measurements were used (mouth width and depth, body width and depth, distance from the top of the mouth to the bottom of the head, head depth, length of the longest gill raker, gut length, standard length and eye diameter) in order to calculate six ecomorphological indices (functional traits) (Table 2). Similarly, for locomotion, biomass of each individual and 11 morphological measurements were used (body depth and width, distance between the centre of the eye to the bottom of the head, head depth, distance between the insertion of the pectoral fin to the bottom of the body, body depth at the level of the pectoral fin insertion, pectoral fin length and surface, caudal fin depth and surface, and caudal peduncle minimal depth) in order to calculate nine ecomorphological indices (functional traits) (Table 2). The small size of individuals (< 2 cm) of Cynodonichthys tenuis prevented the characterization of its food acquisition function; therefore, this species was only characterized for locomotion. Ophisternon aenigmaticum has no external gills and displays anguilliform locomotion, so traits related to fins and the gill raker were considered to be zero for this species. For a complete description of the method, morphological measurements and ecomorphological indices used for functional characterization, see Villéger et al. (2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.).

Table 2
List of functional traits and their ecological meaning. For details of how functional traits were calculated see Villeger et al. (2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.). Bw: body width; Bd: body depth; PFs: pectoral fin surface; CFs: caudal fin surface; 1: Karpouzi & Stergiou (2003Karpouzi, V. S. & K. I. Stergiou. 2003. The relationships between mouth size and shape and body length for 18 species of marine fishes and their trophic implications. Journal of Fish Biology, 62: 1353-1365.); 2: Villéger et al . (2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.); 3: Sibbing & Nagelkerke (2001Sibbing, F. A. & L. A. J. Nagelkerke. 2001. Resource partitioning by Lake Tana barbs predicted from fish morphometrics and prey characteristics. Reviews in Fish Biology and Fisheries, 10: 393-437.); 4: Kramer & Bryant (1995Kramer, D. L. & M. J. Bryant. 1995. Intestine length in the fishes of a tropical stream: 2. Relationships to diet - the long and short of a convoluted issue. Environmental Biology of Fishes, 42: 129-141.); 5: Boyle & Horn (2006Boyle, K. S. & M. H. Horn. 2006. Comparison of feeding guild structure and ecomorphology of intertidal fish assemblages from central California and central Chile. Marine Ecology Progress Series, 319: 65-84.); 6: Gatz (1979Gatz Jr, A. J. 1979. Community organization in fishes as indicated by morphological features. Ecology, 60: 711-718.); 7: Dumay et al. (2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.); 8: Fulton et al. (2001Fulton, C. J., D. R. Bellwood & P. C. Wainwright. 2001. The relationship between swimming ability and habitat use in wrasses (Labridae). Marine Biology, 139: 25-33.); 9: Webb (1984Webb, P. W. 1984. Form and function in fish swimming. Scientific American, 251: 72-82.).

Functional groups. One of the first steps to estimate functional diversity consists of classifying species by functional similarities (Tilman et al., 1997Tilman, D., J. Knops, D. Wedin, P. Reich, M. Ritchie & E. Siemann. 1997. The influence of functional diversity and composition on ecosystem processes. Science, 277: 1300-1302.; Díaz & Cabido, 2001Díaz, S. & M. Cabido. 2001. Vive la différence: plant functional diversity matters to ecosystem processes. Trends in Ecology & Evolution, 16: 646-655.; Dumay et al., 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.). According to Fonseca & Ganade (2001Fonseca, C. R. & G. Ganade. 2001. Species functional redundancy, random extinctions and the stability of ecosystems. Journal of Ecology, 89: 118-125.), classification of species into functional groups requires five steps: (i) defining the classification criteria, in this case, a group of species with similarities in diet and habitat use; (ii) establishing an inclusion criteria (i.e. , defining the biological community), in this study the whole fish assemblage; (iii) choosing key functions, here, locomotion and food acquisition; (iv) choosing the appropriate functional traits that describe the key functions, here summarized as 21 morphological measurements and 15 functional traits (Table 2); (v) constructing a species-trait matrix and applying appropriate multivariate methods to produce functional groups. In this process, each decision can potentially affect the recognition of the functional groups (Fonseca & Ganade, 2001Fonseca, C. R. & G. Ganade. 2001. Species functional redundancy, random extinctions and the stability of ecosystems. Journal of Ecology, 89: 118-125.). Therefore, it is necessary to seek further support for the functional groups based on additional biological information (Dumay et al. , 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.). Here, we contrasted functional groups with published gut contents data (Soto-Galera, 2006Soto-Galera, E. 2006. Ictiofauna de los corredores biológicos Sierra Madre del Sur y Selva Maya Zoque. Comisión Nacional para el Conocimiento y Uso de la Biodiversidad, Y026.; Miller, 2009Miller, R. R. (Ed.). 2009. Peces dulceacuícolas de México. Ciudad de México, Comisión Nacional para el Conocimiento y Uso de la Biodiversidad, 559p.; Schmitter-Soto et al., 2011Schmitter-Soto, J. J., L. E. Ruiz-Cauich, R. L. Herrera & D. González-Solís. 2011. An index of biotic integrity for shallow streams of the Hondo River basin, Yucatan Peninsula. Science of the Total Environment, 409: 844-852.; Hinojosa-Garro et al., 2013Hinojosa-Garro, D., J. Arceo-Gómez, L. Zambrano & L. H. Escalera-Vázquez. 2013. Fish diet composition in permanent and semi-permanent pools in tropical wetlands of the Yucatan Peninsula. Neotropical Ichthyology, 11: 881-890.) to determine trophic groups (Table 1).

Data analysis. We decided to analyse independently similarities in locomotion and in food acquisition in order to achieve a higher detail in niche partitioning. For example, two species may be redundant in one aspect of the niche (i.e. , trophic position) but may differ in the other (i.e. , habitat use). In order to give the same weight to each functional trait, matrices (individuals x functional traits) were standardized (z-transformation), so that the mean of each trait = 0 and its standard deviation = 1 (Villéger et al., 2010Villéger, S., J. R. Miranda, D. F. Hernández & D. Mouillot. 2010. Contrasting changes in taxonomic vs. functional diversity of tropical fish communities after habitat degradation. Ecological Applications, 20: 1512-1522.). A principal component analysis (PCA) was performed separately for each key function using the standardized matrix to identify those functional traits that account for more variation. A cluster analysis based on Ward's Minimum Variance method and Euclidean distances was performed for each key function using the mean values of the first three principal components (Dumay et al., 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.). We used the merging cost to determine the best cut-off distance for each dendrogram (Fränti et al., 2002Fränti, P., O. Virmajoki & T. Kaukoranta. 2002. Branch-and-bound technique for solving optimal clustering. International Conference on Pattern Recognition, 2: 232-235.). To corroborate statistical differences among these groups, we used the first three PCA components and performed a multivariate analysis of variance (MANOVA) with Hotelling's pairwise comparisons, applying the Bonferroni correction. Next, we used locomotion and food acquisition clustering results to delimitate functional groups, i.e. , only species that were clustered in the same group for both functions belonged to the same functional group. In order to compare functional groups richness, diversity and evenness between habitats and seasons, species diversity indices were applied to functional groups (Stevens et al., 2003Stevens, R. D., S. B. Cox, R. E. Strauss & M. R. Willig. 2003. Patterns of functional diversity across an extensive environmental gradient: vertebrate consumers, hidden treatments and latitudinal trends. Ecology Letters, 6: 1099-1108.; Schleuter et al., 2010Schleuter, D., M. Daufresne, F. Massol & C. Argillier. 2010. A user's guide to functional diversity indices. Ecological Monographs, 80: 469-484.). Functional groups richness (FG-richness) represents the number of functional groups found in each pool; functional groups diversity (FG-diversity) was estimated based on the Shannon index; and functional groups evenness (FG-evenness) was estimated using Pielou's evenness index (Morin, 2011Morin, P. J. (Ed.). 2011. Community ecology. Oxford, Wiley Blackwell, 424p.). For each index, differences among the four groups (permanent-dry, permanent-wet, temporary-dry and temporary-wet) were analysed performing a Kruskal-Wallis test followed by a Mann-Whitney U test for pairwise comparisons. All statistical analyses were performed using R software (R Core Team).

Results

During the study, we captured 3,169 individuals representing 14 species in six families (Table 1). These species represent the entire set of species reported for the system in 14 years of sampling (Zambrano et al., 2006Zambrano, L., E. Vázquez-Domínguez, D. García-Bedoya, W. F. Loftus & J. C. Trexler. 2006. Fish community structure in freshwater karstic water bodies of the Sian Ka'an Reserve in the Yucatan peninsula, Mexico. Ichthyological Exploration of Freshwaters, 17: 193-206.; Escalera-Vázquez & Zambrano, 2010Escalera-Vázquez, L. H. & L. Zambrano. 2010. The effect of seasonal variation in abiotic factors on fish community structure in temporary and permanent pools in a tropical wetland. Freshwater Biology, 55: 2557-2569.). For food acquisition, the first three Principal Components described 77 % of the total variation (Table 3). The first Component was strongly correlated with gut length and oral gape shape, which varied inversely. The second Principal Component had a strong correlation with oral gape position and eye size. The third principal component was correlated with the length of the gill raker. For the key function of locomotion, the first three Principal Components accounted for 69 % of the total variation (Table 3). The first Component correlated with aspect ratio of the caudal fin and caudal peduncle throttling. The second Component correlated with fin surface to body size ratio and pectoral fin position. The third Component was correlated with the fin surface ratio.

Table 3
Results of the Principal Component Analysis for the functional traits of the key functions: food acquisition and locomotion. For each Principal Component, the highest correlations (>50) are highlighted in bold.

For the two key functions, four groups were recognized using cluster analysis (Fig. 2). For food acquisition, B. belizanus was the only member of group A (piscivore). All species of group B were identified as omnivore-herbivore and belonged to the same family (Poeciliidae). Group C included three omnivore-carnivore taxonomically unrelated species (A. aeneus , R. octofasciata and R. guatemalensis ). Despite taxonomical differences, three species of Cichlidae and the obscure swamp eel (O. aenigmaticum ) were clustered in the group D (omnivore-carnivore). For locomotion, O. aenigmaticum was the only member of group E (anguilliform locomotion). All species of group F belonged to the same family (Poeciliidae) except C. tenuis (Rivulidae). Group G included two taxonomically unrelated species, A. aeneus (Characidae) and R. guatemalensis (Pimelodidae). Group H included all species of the Cichlidae family. The MANOVA showed significant differences between every group for food acquisition (F (18)=407.8; Λ=0.006; p <0.01) and locomotion (F (27)=435.8; Λ=0.002; p <0.01).

Fig. 2
Cluster analyses of the functional traits data. Dendrograms show groups for food acquisition (A, B, C, and D) and locomotion (E, F, G, and H). Species identities (IDs) correspond to the first letter of the genus and species names.

Considering food acquisition and locomotion together, we determined six functional groups with different ecological characteristics (Table 4). The functional group VI had the highest number of redundant species (5) all of which belong to the Poeciliidae family. Similarly, high redundancy was found within the functional group V, grouping all species from the Cichlidae family, except for R. octofasciata . In contrast, three functional groups were represented by single species: B. belizanus (I), O. aenigmaticum (III) and R. octofasciata (IV). Regardless of taxonomical differences, A. aeneus and R. guatemalensis were representatives of the same functional group (II).

Table 4
Functional groups and their ecological characteristics. Letter A-H: result from clustering analysis. *Based on functional analysis and fish diet presented in Table 1.

We recorded all functional groups in both seasons. However, permanent pools during the dry season presented a significant lower FG-richness (H(3)=956, p<0.05), lower FG- diversity (H(3)=7.86, p<0.05) and higher FG-evenness (H(3)=11.82, p<0.01) (Table 5). During the dry season permanent pools were dominated by group VI (Poeciliidae), and temporary pools by group IV (R. octofasciata ) (Fig. 3). Group II (A. aeneus and R. guatemalensis ) presented low biomass abundance during the dry season and Group I (B. belizanus ) was only present in temporary pools, with low biomass abundance. During the wet season functional group VI dominated in the permanent pools, but group V (Cichlidae) dominated in the temporary pools. All functional groups were detected in temporary pools during the wet season and similar structure was found between habitats, except for an inverse proportion between group V and VI.

Table 5
Diversity indices applied to functional groups. *Significant differences among the four groups (p<0.05).

Fig. 3
Relative biomass abundance of functional groups among habitats and seasons.

Discussion

Our results show functional niche segregation among groups, in both food acquisition and locomotion. After constructing functional groups, high functional redundancy was found within group VI and group V, which are represented by members of the Poeciliidae and Cichlidae families, respectively. Functional redundancy in local communities may lead to greater stability of abundance and biomass over time (Rice et al., 2013Rice, J., N. Daan, H. Gislason & J. Pope. 2013. Does functional redundancy stabilize fish communities?. ICES Journal of Marine Science, 70: 734-742.), since the loss of one species can be compensated by another with a similar function (Tilman et al., 1997Tilman, D., J. Knops, D. Wedin, P. Reich, M. Ritchie & E. Siemann. 1997. The influence of functional diversity and composition on ecosystem processes. Science, 277: 1300-1302.; Hooper et al., 2005Hooper, D. U., F. S. Chapin III, J. J. Ewel, A. Hector, P. Inchausti, S. Lavorel, J. H. Lawton, D. M. Lodge, M. Loreau, S. Naeem, B. Schmid, H. Setälä, A. J. Symstad, J. Vandermeer & D. A. Wardle. 2005. Effects of biodiversity on ecosystem functioning: a consensus of current knowledge. Ecological Monographs, 75: 3-35.). In contrast, group I, III and IV were formed by a single species (B. belizanus , O. aenigmaticum and R. octofasciata , respectively), which represent unique ecological functions in this wetland. The loss or addition of functional unique species directly affects ecosystem processes (Scherer-Lorenzen, 2005Scherer-Lorenzen, M. 2005. Biodiversity and ecosystem functioning: basic principles. In: Barthlott, W., E. Linsenmair & S. Porembski (Eds.). Biodiversity: Structure and Function. Oxford, EOLSS Publishers.), thus, these three species are key to maintain some aspects of the ecosystem functioning.

Not all species were functionally grouped with taxonomical related species. For example, A. aeneus and R. guatemalensis occurred in the same functional group despite being taxonomically unrelated. The classification of species in functional groups transcends taxonomic boundaries, but they are not independent of phylogeny in the sense that frequently species in the same family or genus tend to share common traits (Bellwood et al., 2002Bellwood, D. R., P. C. Wainwright, C. J. Fulton & A. Hoey. 2002. Assembly rules and functional groups at global biogeographical scales. Functional Ecology, 16: 557-562.; Dumay et al., 2004Dumay, O., P. S. Tari, J. A. Tomasini & D. Mouillot. 2004. Functional groups of lagoon fish species in Languedoc Roussillon, southern France. Journal of Fish Biology, 64: 970-983.; Devictor et al., 2010Devictor, V., D. Mouillot, C. Meynard, F. Jiguet, W. Thuiller & N. Mouquet. 2010. Spatial mismatch and congruence between taxonomic, phylogenetic and functional diversity: the need for integrative conservation strategies in a changing world. Ecology Letters, 13: 1030-1040.). Our results showed this dependency between phylogeny and functional attributes within Poeciliidae (omnivore-herbivore and middle-high water column level) and Cichlidae (omnivore-carnivore and middle-low water column level) families. A remarkable exception is B. belizanus (Poeciliidae); the only strict piscivore of the community, this species exhibits a unique function for food acquisition but shares functional attributes of locomotion with other members of the Poeciliidae family (middle-high water column level). Similarly, O. aenigmaticum is the only species with anguilliform locomotion but has food-acquisition attributes similar to members of the Cichlidae family (omnivore-carnivore). These results support the advantages of clustering species independently for locomotion and food acquisition to achieve a higher detail in niche partitioning.

The concept of functional redundancy implies that some species may play similar roles in ecosystems (Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.). However, the functional niche of a given species not only depends on ecological processes related to morphology or physiology but also is modified by demographic attributes and responses to environmental factors (Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.; Violle et al., 2007Violle, C., M. L. Navas, D. Vile, E. Kazakou, C. Fortunel, I. Hummel & E. Garnier. 2007. Let the concept of trait be functional!. Oikos, 116: 882-892.). Additionally, different species may have the same characteristics in some functional aspect, but they can differ in others; therefore, redundancy is reduced among species when considering various functions simultaneously (Gamfeldt et al., 2008Gamfeldt, L., H. Hillebrand & P. R. Jonsson. 2008. Multiple functions increase the importance of biodiversity for overall ecosystem functioning. Ecology, 89: 1223-1231.). In this sense, to be more redundant, two species should belong to the same functional group and have the same range of tolerance to the environment (Rosenfeld, 2002Rosenfeld, J. S. 2002. Functional redundancy in ecology and conservation. Oikos, 98: 156-162.). Under this assumption, it is always possible to separate two species choosing an appropriate niche axis (Morin, 2011Morin, P. J. (Ed.). 2011. Community ecology. Oxford, Wiley Blackwell, 424p.). However, a relevant task for future research consists in identifying the most relevant functional traits linked to ecosystem functioning.

Ours results suggest that environmental conditions during the dry season in permanent pools may act as environmental filters for the fish community, as they had a strong effect on FG-richness, FG-diversity and FG-evenness. Environmental filters restrict both the occurrence and abundance of species (Hooper et al., 2005Hooper, D. U., F. S. Chapin III, J. J. Ewel, A. Hector, P. Inchausti, S. Lavorel, J. H. Lawton, D. M. Lodge, M. Loreau, S. Naeem, B. Schmid, H. Setälä, A. J. Symstad, J. Vandermeer & D. A. Wardle. 2005. Effects of biodiversity on ecosystem functioning: a consensus of current knowledge. Ecological Monographs, 75: 3-35.; Mouillot et al., 2006Mouillot, D., O. Dumay & J. A. Tomasini. 2006. Limiting similarity, niche filtering and functional diversity in coastal lagoon fish communities. Estuarine, Coastal and Shelf Science, 71: 443-456.; Mason et al., 2008Mason, N. W. H., C. Lanoiselée, D. Mouillot, J. B. Wilson & C. Argillier. 2008. Does niche overlap control relative abundance in French lacustrine fish communities? A new method incorporating functional traits. Journal of Animal Ecology, 77: 661-669.). Therefore, when environmental filters are strong drivers of community structure, the most abundant species have similar niches, allowing them to tolerate harsh conditions (Zobel, 1997Zobel, M. 1997. The relative role of species pools in determining plant species richness. An alternative explanation of species coexistence?. Trends in Ecology & Evolution, 12: 266-269.; Mason et al ., 2008Mason, N. W. H., C. Lanoiselée, D. Mouillot, J. B. Wilson & C. Argillier. 2008. Does niche overlap control relative abundance in French lacustrine fish communities? A new method incorporating functional traits. Journal of Animal Ecology, 77: 661-669.). Previous studies have shown that even though permanent pools are connected to groundwater, environmental conditions are characterized by a very low concentration of dissolved oxygen (Escalera-Vázquez & Zambrano, 2010Escalera-Vázquez, L. H. & L. Zambrano. 2010. The effect of seasonal variation in abiotic factors on fish community structure in temporary and permanent pools in a tropical wetland. Freshwater Biology, 55: 2557-2569.). These pools were dominated by functional group VI (Poeciliidae), which can tolerate extreme conditions of salinity, temperature and hypoxia (Meffe & Snelson, 1989Meffe, G. K. & F. F. Snelson (Eds.). 1989. Ecology and Evolution of Livebearing Fishes (Poeciliidae). Englewood Cliffs, Prentice Hall, 424p.), whereas the species of group III (O. aenigmaticum ) is a facultative air-breather (Ishimatsu, 2012Ishimatsu, A. 2012. Evolution of the cardiorespiratory system in air-breathing fishes. Aqua-BioScience Monographs, 5: 1-28.).

As we hypothesized, functional group structure was modified in permeant pools during the dry season, when low dissolved oxygen concentration may act as an environmental filter. In contrast, during the wet season, substantial expansion of habitat occurred and all pools were completely connected for at least two months (August and September). During this season, our results show a stable functional group structure between habitats, a higher FG-richness and FG-diversity, and niche partitioning among the structure of functional groups. These results support the idea that floods reduce spatial variability among local communities (Thomaz et al., 2007Thomaz, S. M., L. M. Bini & R. L. Bozelli. 2007. Floods increase similarity among aquatic habitats in river-floodplain systems. Hydrobiologia, 579: 1-13.), and suggest a high availability of food sources and favourable environmental conditions. Functional niche partitioning may result in a compatible use of resources (Tilman, 1982Tilman, D. (Ed.). 1982. Resource Competition and Community Structure. Princeton, Princeton University Press, 296p.; Mason et al., 2007Mason, N. W. H., C. Lanoiselée, D. Mouillot, P. Irz & C. Argillier. 2007. Functional characters combined with null models reveal inconsistency in mechanisms of species turnover in lacustrine fish communities. Oecologia, 153: 441-452.; Córdova-Tapia et al., 2015Córdova-Tapia, F., M. Contreras & L. Zambrano. 2015. Trophic niche overlap between native and non-native fishes. Hydrobiologia, 746: 291-301.), which allow species to coexist (MacArthur & Levins, 1967MacArthur, R. & R. Levins. 1967. The limiting similarity, convergence, and divergence of coexisting species. The American Naturalist, 101: 377-385.), thus leading to an increase in ecosystem productivity and nutrient retention (Hooper et al., 2005Hooper, D. U., F. S. Chapin III, J. J. Ewel, A. Hector, P. Inchausti, S. Lavorel, J. H. Lawton, D. M. Lodge, M. Loreau, S. Naeem, B. Schmid, H. Setälä, A. J. Symstad, J. Vandermeer & D. A. Wardle. 2005. Effects of biodiversity on ecosystem functioning: a consensus of current knowledge. Ecological Monographs, 75: 3-35.; Scherer-Lorenzen, 2005Scherer-Lorenzen, M. 2005. Biodiversity and ecosystem functioning: basic principles. In: Barthlott, W., E. Linsenmair & S. Porembski (Eds.). Biodiversity: Structure and Function. Oxford, EOLSS Publishers.). Further research is needed to test these particular hypotheses related to assembly rules in different habitats and seasons.

Functional groups based on species similarities in food acquisition and locomotion allowed us to understand niche partitioning within a community. This was useful to determine functional redundancy, which was not strictly dependent on taxonomical identities. In this tropical wetland, the hydrological dynamic changes functional groups structure, particularly in permanent pools during the dry season, where environmental filtering may play an essential role shaping community assembly.

Acknowledgements

Research funded by Universidad Nacional Autónoma de México - Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica (PAPPIT-IN206114) and Consejo Nacional para la Ciencia y Tecnología (CONACYT) through Posgrado en Ciencias Biológicas (UNAM; Scholarship 280585). We thank Amigos de Sian Ka'an A. C. and the Comisión Nacional de Áreas Naturales Protegidas (CONANP) for facilities and support. Thanks to Karen Levy, Luis Escalera and Angel Merlo for their comments on an early version of the manuscript. We are grateful to Rodrigo Pacheco, Daniel Manzur, Julio Díaz, Carlos Sumano, Nuria Pérez, Pablo López, Victor Hernández, Shanty Acosta and Jorge Jiménez for their hard work during field sessions. Sampling permit: SEMARNAT FAUT-0112.

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Publication Dates

  • Publication in this collection
    2016

History

  • Received
    02 Oct 2015
  • Accepted
    11 Apr 2016
Sociedade Brasileira de Ictiologia Neotropical Ichthyology, Núcleo de Pesquisas em Limnologia, Ictiologia e Aquicultura, Universidade Estadual de Maringá., Av. Colombo, 5790, 87020-900, Phone number: +55 44-3011-4632 - Maringá - PR - Brazil
E-mail: neoichth@nupelia.uem.br