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Invasive poeciliids dominate fish community in a highly altered river: insights from a diversity study of riverbank fishes in Mexico

Abstract

The presence of invasive species can cause significant changes in native communities and ecosystem functions. Mexico is home to 6% of all known freshwater fish species on the planet, with a high rate of endemism. Due to heavy urbanization, the Mexican Central Plateau has become one of the most densely populated areas in the world, and its Tula River is considered one of the most polluted rivers in Mexico. Our objective was to investigate whether native fish species persist in such adverse conditions and to evaluate the seasonal and spatial distribution of both native and non-native species at three sites along the Tula River. We evaluated environmental characteristics and fish community structure. We found two native species, the black fin goodea (Goodea atripinnis) and the yellow shiner (Notropis calientis). However, their abundance was extremely low across all sites and seasons. In contrast, invasive poecilids dominated the communities, accounting for 99.4% of the total abundance. Our results indicate a clear relationship between river characteristics and fish community structure, highlighting the significance of river width, river velocity, temperature, dissolved oxygen, and pH. The prevalence of invasive species underscores the urgent need for conservation efforts aimed to protect and restore native fish populations.

Anthropogenic alteration; Goodeids; Invasion success; Tula River

Resumen

La presencia de especies invasoras puede causar cambios significativos en las comunidades nativas y en las funciones de los ecosistemas. México alberga el 6% de todas las especies de peces conocidas en el planeta, con una alta tasa de endemismo. Debido a la fuerte urbanización, el Altiplano mexicano se ha convertido en una de las áreas más densamente pobladas del mundo, y su río Tula es considerado uno de los ríos más contaminados de México. Nuestro objetivo fue investigar si las especies de peces nativos persisten en estas condiciones adversas y evaluar la distribución estacional y espacial de las especies, tanto nativas como no nativas, en tres sitios a lo largo del río Tula. Evaluamos características ambientales y la estructura de la comunidad de peces. Encontramos dos especies nativas, el Tiro (Goodea atripinnis) y la carpita amarilla (Notropis calientis). Sin embargo, sus abundancias se encontraron extremadamente bajas en todos los sitios y estaciones. En contraste, los poecílidos invasores dominaron las comunidades en todos los sitios y estaciones, representando el 99,4% de la abundancia total. Nuestros resultados indican una clara relación entre las características del río y la estructura de la comunidad de peces, resaltando la importancia del ancho del río, la velocidad del río, la temperatura, el oxígeno disuelto y el pH. La prevalencia de especies invasoras resalta la necesidad urgente de esfuerzos de conservación dirigidos a proteger y restaurar las poblaciones de peces nativos.

Palabras clave:
Alteración antropogénica; Éxito de invasión; Goodeidos; Río Tula

INTRODUCTION

Freshwater ecosystems are under extreme social, political, and economic pressure worldwide, since almost all human activities are closely connected to water (Reid et al., 2019Reid AJ, Carlson AK, Creed IF, Eliason EJ, Gell PA, Johnson PT et al. Emerging threats and persistent conservation challenges for freshwater biodiversity. Biol Rev Camb Philos Soc. 2019; 94(3):849–73. https://doi.org/10.1111/brv.12480
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). The environmental and ecological stress in rivers is primarily due to the influence of human settlements, with increased poverty contributing to greater dependency on the ecosystem services provided by water and its nutrients (Kondolf et al., 2018Kondolf GM, Schmitt RJP, Carling P, Darby S, Arias M, Bizzi S et al. Changing sediment budget of the Mekong: Cumulative threats and management strategies for a large river basin. Sci Total Environ. 2018; 625:114–34. https://doi.org/10.1016/j.scitotenv.2017.11.361
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; Best, 2019Best J. Anthropogenic stresses on the world’s big rivers. Nat Geosci. 2019; 12:7–21. https://doi.org/10.1038/s41561-018-0262-x
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). The use of water resources imposes numerous modifications to the morphology of rivers, such as the construction of dams and irrigation canals. The quality of water in watersheds is affected by land use, with agriculture, industry, urbanization, and deforestation representing the primary sources of point and diffuse pollution. This, in turn, affects aquifer storage and water quality (Aguilar-Ibarra, 2010Aguilar-Ibarra A. Calidad del agua: un enfoque multidisciplinario. México, D.F.: Universidad Nacional Autónoma de México (UNAM), Instituto de Investigaciones Económicas Restauración Ecológica y Desarrollo (REDES); 2010. ).

Anthropogenic alteration of rivers including pollution, overexploitation, habitat modification and the introduction of exotic species, induce changes in rivers that significantly impact their resilience (Arnell, Gosling, 2016Arnell NW, Gosling SN. The impacts of climate change on river flood risk at the global scale. Clim Change. 2016; 134:387–401. https://doi.org/10.1007/s10584-014-1084-5
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). Moreover, some of these stressors act synergistically, with habitat fragmentation and pollution posing a threat to the survival of native species and facilitating the arrival and establishment of exotic species that can later become invasive. These invasive species often possess traits that enable them to thrive and dominate in human-disturbed environments. As a result, they can outcompete native species, potentially causing further ecological imbalances (Simberloff et al., 2013Simberloff D, Martin JL, Genovesi P, Maris V, Wardle DA, Aronson J et al. Impacts of biological invasions: what’s what and the way forward. Trends Ecol Evol. 2013; 28(1):58–66. https://doi.org/10.1016/j.tree.2012.07.013
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).

The presence of invasive species often results in a significant alteration of native communities and ecosystem functions, which in turn results in biodiversity losses and ecological integrity through predation, competition, disease transmission, and habitat degradation (Early et al., 2016Early R, Bradley BA, Dukes JS, Lawler JJ, Olden JD, Blumenthal DM et al. Global threats from invasive alien species in the twenty-first century and national response capacities. Nat Commun. 2016; 7(12485):1–09. https://doi.org/10.1038/ncomms12485
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). These changes lead to important economic costs, more than US$26 billion annually (Diagne et al., 2021Diagne C, Leroy B, Vaissière A-C, Gozlan RE, Roiz D, Jarić I et al. High and rising economic costs of biological invasions worldwide. Nature. 2021; 592(7855):571–76. https://doi.org/10.1038/s41586-022-05100-6
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), and an interruption in productivity and nutrient availability cycles within the habitat, affecting trophic structure and population dynamics (Parker et al., 1999Parker IM, Simberloff D, Lonsdale WM, Goodell K, Wonham M, Kareiva PM et al. Impact: Toward a framework for understanding the ecological effects of invaders. Biol Invasions. 1999; 1:3–19. https://doi.org/10.1023/A:1010034312781
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). The introduction and establishment of invasive species can have almost immediate ecological effects and economic consequences that are increased by the interconnection between rivers (Bernery et al., 2022Bernery C, Bellard C, Courchamp F, Brosse S, Gozlan RE, Jarić I et al. Freshwater fish invasions: A comprehensive review. Annu Rev Ecol Evol Syst. 2022; 53(1):427–56. https://doi.org/10.1146/annurev-ecolsys-032522-015551
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).

The conservation status of freshwater ecosystems in Mexico is critical, as evidenced by the fact that approximately 70% of water bodies are contaminated to some degree by urban and industrial discharges (Conagua, 2018Comisión Nacional del Agua (Conagua). Estadísticas del agua en México, edición 2017. Ciudad de México, México: Secretaría del Medio Ambiente y Recursos Naturales; 2018. ). Furthermore, almost half of the rivers and streams in the country are classified as having a high or very high degree of ecohydrological alteration (Garrido et al., 2010Garrido A, Pérez DJL, Enríquez C. Delimitación de zonas funcionales de las cuencas hidrográficas de México. In: Cotler H, editor. Las cuencas hidrográficas de México. Diagnóstico y priorización. México: Instituto Nacional de Ecología/Fundación Gonzalo Río Arronte I.A.P. 2010. p.14–17. ). Water pollution in Mexican rivers is caused by various sources, such as the discharge of urban waste, including pharmaceutical products, mining (which contribute with heavy metals) and agricultural activities that involve the use of harmful pesticides (Balderas et al., 2017Balderas ECS, Hernandez MAA, Berti-Equille L, Grac C, Desconnets JC. Evaluation of heavy metals, pesticides and emergent pollutants content in the Tula River, Mexico. Proceedings of the 10th European Symposium for Freshwater Sciences; 2017. ).

Freshwater fish species have been relatively neglected in terms of conservation efforts (Beltrán-López et al., 2023Beltrán-López RG, García-Andrade AB, Ornelas-García CP. Mexican freshwater fishes in the Anthropocene. In: Jones RW, Ornelas-Garcia CP, Pineda-López R, Álvarez F, editors. Mexican fauna in the Anthropocene. Cham: Springer International Publishing. 2023. p.129–52. ). This lack of attention has resulted in these species being among the most threatened in the context of global change. With around 506 species distributed in 47 families, Mexico represents 6% of the total known species on the planet, with a high rate of endemism (163 species, 32%) (Dudgeon et al., 2006Dudgeon D, Arthington AH, Gessner MO, Kawabata Z-I, Knowler DJ, Lévêque C et al. Freshwater biodiversity: importance, threats, status and conservation challenges. Biol Rev Camb Philos Soc. 2006; 81(2):163–82. https://doi.org/10.1017/S1464793105006950
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). Despite their importance, Mexico’s freshwater fish diversity faces significant threats. For instance, at least 33% of these species are considered at risk of extinction (De la Vega-Salazar, 2006De la Vega-Salazar M. Conservation status of Goodeidae family fishes (Cyprinodontiformes) from the Mexican Central Plateau. Rev Biol Trop. 2006; 54(1):163–77. ). The Mexican Central Plateau is home to 11 families, of which the Goodeidae family is the highest in endemism with 36 species (Domínguez-Domínguez et al., 2006Domínguez-Domínguez O, Martínez-Meyer E, Zambrano L, Pérez-Ponce de León G. Using ecological-niche modeling as a conservation tool for freshwater species: Live-bearing fishes in central Mexico. Conserv Biol. 2006; 20(6):1730–39. https://doi.org/10.1111/j.1523-1739.2006.00588.x
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). Unfortunately, almost all Goodeidae species are in protected conservation status, and some are already extinct in the wild (Suárez-Rodríguez et al., 2023Suárez-Rodríguez M, del-Val E, Domínguez-Domínguez O, Ojanguren AF, Camacho-Cervantes M. Population growth and behavioural interactions of a critically endangered fish with co-occurring native and exotic species. Freshw Biol. 2023; 68(4):698–710. https://doi.org/10.1111/fwb.14057
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).

The Mexican Central Plateau is highly urbanized, leading to contamination from wastewater, agricultural, and industrial activities associated with major cities such as Mexico City (UN, 2019United Nations (UN). World Urbanization Prospects 2018: Highlights. Department of Economic and Social Affairs, Population Division. 2019.). Consequently, the Moctezuma River basin is considered the most impacted by human activities in the country (Gutiérrez-Yurrita et al., 2013Gutiérrez-Yurrita PJ, Morales-Ortiz JA, Marín-García L. Diversidad biológica, distribución y estrategias de conservación de la ictiofauna de la cuenca del río Moctezuma, Centro de México. Limnetica. 2013; 32(2):215–28. https://doi.org/10.23818/limn.32.18
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). Furthermore, the establishment and dispersion of invasive species, loss of habitat, and restricted or specialized tolerance ranges also threaten the permanence of native species in the area (Magurran, 2009Magurran AE. Threats to freshwater fish. Science. 2009; 325(5945):1215–16. https://doi.org/10.1126/science.1177215
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; Carrillo, García, 2015Carrillo ER, Garcia CM. Limited options for native goodeid fish simultaneously confronted to climate change and biological invasions. Biol Invasions. 2015; 17(1):245–56. https://doi.org/10.1007/s10530-014-0723-0
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; Gesundheit, Macías-Garcia, 2018Gesundheit P, Macías-Garcia C. The role of introduced species in the decline of a highly endemic fish fauna in Central Mexico. Aquat Conserv. 2018; 28(6):1384–95. https://doi.org/10.1002/aqc.2927
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).

Poeciliids are among the most widespread invasive freshwater fish in the Mexican Central Plateau, they are small viviparous fish that share some ecological requirements with some native species like Goodeids. One of the most researched poeciliids is the guppy Poecilia reticulata Peters, 1859, which was introduced to the region in an attempt to control mosquito larvae and as the result of discarding unwanted pets (Azevedo-Santos et al., 2016Azevedo-Santos VM, Vitule JRS, Pelicice FM, García-Berthou E, Simberloff D. Nonnative fish to control Aedes mosquitoes: A controversial, harmful tool. BioScience. 2016; 67(1):84–90. https://doi.org/10.1093/biosci/biw156
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). This is a species with a natural range of distribution in Trinidad, Guyana, Venezuela, and Suriname (Magurran, 2005Magurran AE, Ramnarine IW. Evolution of mate discrimination in a fish. Curr Biol. 2005; 15(21):867–68. https://doi.org/10.1016/j.cub.2005.10.034
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), but it is currently present in all continents except Antarctica (Deacon et al., 2011Deacon AE, Ramnarine IW, Magurran AE. How reproductive ecology contributes to the spread of a globally invasive fish. PloS ONE. 2011; 6(9):e24416. https://doi.org/10.1371/journal.pone.0024416
https://doi.org/10.1371/journal.pone.002...
). Although the guppy is a well-known invasive poeciliid in the Mexican Central Plateau, it is not the only invasive poeciliid species in the region. For instance, the twospot livebearer Pseudoxiphophorus bimaculatus (Heckel, 1848) and the porthole livebearer Poeciliopsis gracilis (Heckel, 1848) are also found in the Tula River (Camacho-Cervantes et al., 2019Camacho-Cervantes M, Palomera-Hernadez V, García CM. Foraging behaviour of a native topminnow when shoaling with invaders. Aquatic Invasions. 2019; 14(3):490–501. Available from: https://www.reabic.net/aquaticinvasions/2019/AI_2019_CamachoCervantes_etal.pdf
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). Like guppies, these species have high reproductive rates and phenotypic plasticity, which enables them to establish and grow populations quickly (Gómez-Márquez et al., 2007Gómez-Márquez JL, Peña Mendoza B, Salgado Hugarte IH, Sánchez Herrera AK, Sartré Baez L. Reproduction of the fish Poeciliopsis gracilis (Cyprinodontiformes: Poeciliidae) in Coatetelco, a tropical shallow lake in Mexico. Rev Biol Trop. 2007; 56(4):1801–12. ). Poeciliids mainly inhabit rivers and shallow ponds and possess many physiological, behavioral, and life history traits associated with a broad habitat range (Camacho-Cervantes et al., 2018Camacho-Cervantes M, Ojanguren AF, Domínguez-Domínguez O, Magurran AE. Sociability between invasive guppies and native topminnows. PLoS ONE. 2018; 13(2):e0192539. https://doi.org/10.1371/journal.pone.0192539
https://doi.org/10.1371/journal.pone.019...
; Aceves-Fonseca et al., 2022Aceves-Fonseca E, Santiago-Arellano A, Camacho-Cervantes M. Sex, size and habitat complexity effects on emergence latency and latency to locate food of the invasive porthole livebearer (Poeciliopsis gracilis). PLoS ONE. 2022; 17(6):e0269384. https://doi.org/10.1371/journal.pone.0269384
https://doi.org/10.1371/journal.pone.026...
). In contrast, native species tend to have slower reproductive rates and be highly specialized, putting them at a disadvantage when facing a poeciliid invasion (Lyons et al., 2019Lyons J, Piller KR, Artigas-Azas JM, Dominguez-Dominguez O, Gesundheit P, Köck M et al. Distribution and current conservation status of the Mexican Goodeidae (Actinopterygii, Cyprinodontiformes). ZooKeys. 2019; 885:115–58. https://doi.org/10.3897/zookeys.885.38152
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; Ramírez-García et al., 2020Ramírez-García A, Piller K, Ramírez-Herrejón JP, Medina-Nava M, Hernández-Morales R, Domínguez-Domínguez O. Reproductive biology of three native livebearer fish species (Actinopterygii: Cyprinodontiformes: Goodeidae) in the Teuchitlán River, Mexico. Acta Ichthyol Piscat. 2020; 50(1):1–12. https://doi.org/10.3750/AIEP/02513
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).

The Tula River stands out as one of Mexico’s most anthropogenically altered rivers, contending with the inflow of all wastewaters from Mexico City and industrial discharges from Tula City (Ortiz-Gallarza, Ramírez-López, 2003Ortiz-Gallarza SM, Ramírez-López JA. Water quality of the Tula River related to the petroleum refining industry: accumulation factors and treatments. WIT Trans Ecol Environ. 2003; 65:67–77. ; Casanova et al., 2008Casanova RM, Martínez AJG, Sánchez EMO, Ibarra JRV, Sandoval OAA, García FP. Modelación de la calidad del agua del Río Tula, Estado de Hidalgo, México. Dyna. 2008; 75(154):5–18. ). Its water plays a crucial role in irrigating the Mezquital Valley and eventually finds its way to the Zimapán dam (Rubio-Franchini et al., 2016Rubio-Franchini I, López-Hernández M, Ramos-Espinosa MG, Rico-Martínez R. Bioaccumulation of metals arsenic, cadmium, and lead in zooplankton and fishes from the Tula River watershed, Mexico. Water Air Soil Pollut. 2016; 227(5):1–12. https://doi.org/10.1007/s11270-015-2702-1
https://doi.org/10.1007/s11270-015-2702-...
). Previous studies in the region have shown that the Tula River has the lowest species richness and abundance among water bodies in the Moctezuma River basin (Gutiérrez-Yurrita et al., 2013Gutiérrez-Yurrita PJ, Morales-Ortiz JA, Marín-García L. Diversidad biológica, distribución y estrategias de conservación de la ictiofauna de la cuenca del río Moctezuma, Centro de México. Limnetica. 2013; 32(2):215–28. https://doi.org/10.23818/limn.32.18
https://doi.org/10.23818/limn.32.18...
). In our study, we selected three specific sites along the Tula River to investigate whether native fish species persist in such adverse conditions and to evaluate the seasonal and spatial distribution of both native and non-native species at three sites along the Tula River.

MATERIAL AND METHODS

Study area. The Tula River runs from the state of Estado de Mexico to the central-southern region of Hidalgo, plays a crucial role in the Panuco Hydrological Region which flows into the Gulf of Mexico (Rubio-Franchini et al., 2016Rubio-Franchini I, López-Hernández M, Ramos-Espinosa MG, Rico-Martínez R. Bioaccumulation of metals arsenic, cadmium, and lead in zooplankton and fishes from the Tula River watershed, Mexico. Water Air Soil Pollut. 2016; 227(5):1–12. https://doi.org/10.1007/s11270-015-2702-1
https://doi.org/10.1007/s11270-015-2702-...
). Three distinct study sites were chosen along this watercourse (Fig. 1): 1) Dam spillway (20º09’58”N 99º21’29”W) is situated at the spillway of Endho Dam, influenced by both excess overflow and seepage. Endho Dam receives sewage from Mexico City through both the Central Emitter and the East Emitter. Additionally, it receives discharges from the industrial and urban areas of Tula City, as well as from a refinery and a thermoelectric power plant. Locals commonly describe this dam as an “environmental hell” due to the severe pollution; 2) Spring-fed (20º10’50”N 99º20’26”W) is located downstream from Endho, alongside Binola town. This site is situated in a region abundant with natural springs, contributing to enhanced water quality. The area is surrounded by crop fields, utilizing water for various agricultural activities; 3) Drainage confluence (20º14’26”N 99º13’48”W) is situated downstream within the urban perimeter of Mixquiahuala town. This site serves as a recreational area for locals. However, it is positioned after the confluence with the Salado River, where Tula River receives the remaining portion of the drainage from Mexico City, previously conveyed through the Grand Canal.

Sampling methods. Sampling was conducted at different time points to capture the varying environmental conditions prevalent during the dry hot season in April, the rainy season in July, and the dry cold season in November, all within the year 2019. Each site was visited and sampled once during each of these three distinct seasons. To comprehensively characterize the environmental conditions of each site, multiple parameters were measured. These parameters included the width of the river (m), the river velocity (m/s), dissolved oxygen concentration (mg/L), temperature (°C), and pH. To obtain a representative average of the river’s velocity (m/s), we utilized the floating method at various depths (~1.2 m) across the river. For measuring dissolved oxygen, a microprocessor-based probe (HI–9146, Hanna Instruments) was employed. Additionally, temperature and pH measurements were obtained using a multiparameter sonde (HI–991300, Hanna Instruments), which allowed for simultaneous data collection. Sondes were placed at 20 cm below water surface. All environmental data were collected at the fish sampling sites and during the same period.

FIGURE 1 |
Map of the sampling sites along the Tula River: 1) Dam spillway, 2) Spring-fed, 3) Drainage confluence.

Fish sampling proceeded in a standardized approach following the Standard Methods for Sampling North American Freshwater Fishes (Bonar et al., 2009Bonar SA, Hubert WA, Willis DW. Standard methods for sampling North American freshwater fishes. American Fisheries Society, Bethesda, Maryland. 2009. ). Six unbaited Gee’s minnow traps (42 cm, 2 mm mesh) with funnel entrance diameter of 3 cm were set for four 15-min periods. Additionally, a single fisher used a hand net (49 x 39 cm, 3 x 4 mm mesh size) to capture individuals within a 30-min period. Sampling was conducted at least three meters away from where the fish traps were placed, and approximately 30 hand net launches were carried out during each sampling event. The section of the river within which the samples were taken covered a length of approximately 30 m in each site.

Sampling sites were selected to cover all possible available habitats along the riverbank. Fish surveys were conducted during daylight hours (between 10:00 and 13:00) from Monday to Friday to avoid interference from recreational visitors. At the end of each sampling period, individuals were collected, identified, and then released on-site to avoid disrupting the community structure. These methods were chosen because in this area the river is relatively small (width ~30 m) and shallow (~50 cm).

Statistical analyses. The fish data were standardized by sampling time to enable comparison of the percentage of individuals found in each site and season. To ensure the representativeness of the sampling effort, species accumulation curves (SAC) were constructed for each site and season. In order to describe the fish communities, we used species richness, abundance, and calculated Shannon diversity index (H), Simpson dominance index (D) and beta diversity (Whittaker). To compare the abundance of each species within sites and seasons, rank abundance curves were generated. For the drainage confluence site, a logarithm was applied due to the relatively large number of individuals recorded across all seasons. We performed a Canonical Correspondence Analysis (CCA) to examine the relationships between environmental conditions as explanatory variables and fish abundance as response variables for each site and season. In addition, Pearson correlations were performed between environmental variables and community indexes using data from every site and season. Community analyses were performed using the “vegan” package within the R statistical software (R Development Core Team, 2020R Development Core Team. R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing; 2020. Available from: https://www.R-project.org
https://www.R-project.org...
).

RESULTS

The fish community along the riverbank consisted of seven species, out of which two were native, namely the blackfin goodea, Goodea atripinnis Jordan, 1880, and the yellow shiner, Notropis calientis Jordan & Snyder, 1899; and five of them are invasive, the guppy, Poecilia reticulata, the twospot livebearer, Pseudoxiphophorus bimaculatus, the porthole livebearer, Poeciliopsis gracilis, the shortfin molly, Poecilia mexicana Steindachner, 1863, and the common carp, Cyprinus carpio Linnaeus, 1758. The species accumulation curves for each site and season show that the sampling method was adequate and sufficient (Fig. S1).

The dam spillway site lacked any native species, while in spring-fed and drainage confluence sites, native species were present but in extremely low numbers constituting only 0.64% and 1.09% of the overall abundance, respectively (Tab. 1). Across all sites, the most dominant species was an invasive one: P. bimaculatus (dam spillway), P. mexicana (spring-fed) and P. reticulata (drainage confluence). Overall, invasive species accounted for 99.4% of the total abundance.

TABLE 1 |
Species present in the Tula River, the total number of individuals collected at each site and their respective percentages.

Our data showed that native species are persisting in very low abundances within the studied sites and seasons (Fig. 2; Tab. S2). In dam spillway site, the native species were absent. In spring-fed site, both native species were present, but with G. atripinis observed only during the rainy season and N. calientis during the dry hot season. In drainage confluence site, G. atripinis was present during all three seasons, but in relatively low numbers in contrast with invasive species. In dam spillway site, P. bimaculatus dominated during both dry hot and rainy seasons, while during the dry cold season, P. gracilis dominated. Similarly, in spring-fed site P. mexicana dominate during the same dry hot and rainy seasons, while P. reticulata dominated during the dry cold season. Interestingly, in drainage confluence site, P. reticulata dominated in all three seasons.

Among the different sites, dam spillway had the lowest species richness and abundance, while spring-fed showed higher numbers and even more so in drainage confluence (Tab. 2). However, drainage confluence site exhibited the lowest values of diversity and highest of dominance, with P. reticulata being the most abundant species across all seasons. In contrast, spring-fed site showed the evenest distribution of species, with the lowest dominance index recorded being 0.31 during the dry hot season. The analysis of beta diversity revealed that, overall, there is greater spatial than temporal variation in species composition (Tab. S3). The site with the greatest difference was the dam spillway during the dry cold season, as only two species were recorded: P. gracilis and P. reticulata. High similarity was observed between the dam spillway during the dry hot and dry rainy seasons, as well as among the three seasons of the drainage confluence site. Among sites, there was a notable similarity between spring-fed during the rainy and dry cold seasons and drainage confluence across all three seasons.

FIGURE 2 |
Rank-abundance curves for each site and each sampled season. Pb: Pseudoxiphophorus bimaculatus; Pr: Poecilia reticulata; Pg: P. gracilis; Pm: P. mexicana; Ga: Goodea atripinnis; Nc: Notropis calientis, Cc: Cyprinus carpio. Native species are highlighted in bold. Due to the high number of individuals in drainage confluence site Log10 was used for comparative purposes.
TABLE 2 |
Environmental characteristics and community indexes for each site and season.


Our results indicate significant positive correlations between river width and temperature (r = 0.70, p = 0.03) and diversity (r = 0.72, p = 0.02), as well as significant negative correlations with dissolved oxygen (r = -0.67, p = 0.04) and dominance (r = -0.73, p = 0.02). Furthermore, the study revealed that the abundance was positively correlated with both river velocity (r = 0.89, p = 0.001) and pH levels (r = 0.67, p = 0.04). Additionally, the temperature was positively associated with species richness (r = 0.69, p = 0.03) and negatively related to dissolved oxygen (r = -0.80, p = 0.009) (Tab. 2).

The results of Canonical Correspondence Analysis (CCA) provided valuable insights into the relationship between environmental characteristics and fish community structure across different sites and seasons (Fig. 3). The first and second axes of the CCA explained 98% of the total variance (with 76% attributed to CCA1 and 22% to CCA2; Tab. S4). CCA1 positive scores were strongly associated with pH (0.87) and river velocity (0.66), while showing a negative relation with river width (-0.33). These positive components of CCA1 were consistently associated to the presence of G. atripinnis and P. reticulata and the drainage confluence site throughout all seasons. Conversely, the negative side of CCA1 was associated with the dam spillway site across all seasons, with a prevalence of P. bimaculatus and P. gracilis. Additionally, the negative side of CCA1 was also linked to the spring-fed site during the dry hot and rainy seasons and with the presence of N. calientis, C. carpio, and P. mexicana. CCA2 positive scores were mainly influenced by Temperature (0.53) and river width (0.41), while displaying a negative relationship with river velocity (-0.2). This allowed for a clear differentiation between the spring-fed and dam spillway sites.

FIGURE 3 |
Canonical Correspondence Analysis (CCA) results showing the relative influence of environmental variable on the community structure of fish species within each site and seasons. Native species are represented by black triangles, while invasive species are denoted by black circles

DISCUSSION

We found the Tula River to be extensively invaded, with only two native species persisting: the blackfin goodea (G. atripinnis) and the yellow shiner (N. calientis), but they only account for a maximum of 1% of total abundances. Historical inventories of native species in the heavily altered Tula River are scarce, hampering a comprehensive understanding of pre-existing biodiversity and its abundance. Our findings confirm a decline in native species likely due to anthropogenic alteration and competition with invasive species.

From the two native species found in our site, N. calientis is the rarest. Its conservation status was recently evaluated for the IUCN Red List, where it was classified as Critically Endangered (Domínguez, 2019Domínguez O.. Notropis calientis. The IUCN Red List of Threatened Species; 2019. Available from: https://www.iucnredlist.org/es/species/191275/1974814
https://www.iucnredlist.org/es/species/1...
). Interestingly, N. calientis was found only in spring-fed, a site that is influenced by water springs along the riverbed. It was neither found in dam spillway site Endho, where only invasive species were found, nor in drainage confluence site, where the water from Saldo River is incorporated. Considering this, we believe that the subsistence of N. calientis is related to some aspects of water quality. Contrastingly, G. atripinnis is a widely distributed goodeid species in central Mexico (Miller et al., 2009Miller RR, Minckley WL, Norris SM, Gach MH. Peces dulceacuícolas de México. Tlalpan, México, D.F: Comisión Nacional para el Conocimiento y Uso de la Biodiversidad Sociedad Ictiológica Mexicana El Colegio de la Frontera Sur Desert Fishes Council; 2009. ), it holds a conservation status of Least Concern according to the most recent evaluation on the IUCN Red List (Koeck, Maiz-Tome, 2019Koeck M, Maiz-Tome L.. Goodea atripinnis. The IUCN red list of threatened species. 2019. Available from: https://www.iucnredlist.org/es/species/133768576/1276740
https://www.iucnredlist.org/es/species/1...
). This species is known for its adaptability to challenging conditions (Ramírez-García et al., 2021Ramírez-García A, Moncayo-Estrada R, González-Cárdenas JJ, Domínguez-Domínguez O. Reproductive cycle of native viviparous fish species (Actinopterygii: Cyprinodontiformes: Goodeidae) in a subtropical Mexican lake. Neotrop Ichthyol. 2021; 19(4):e210105. https://doi.org/10.1590/1982-0224-2021-0105
https://doi.org/10.1590/1982-0224-2021-0...
) and its reputation as one of the most tolerant species within its family (Silva-Santos et al., 2016Silva-Santos J.R, Martínez-Saldaña MC, Rico-Martínez R, Gómez-Márquez JL, Arredondo-Figueroa JL. Reproductive biology of Goodea atripinnis (Jordan, 1880) (Cyprinodontiformes: Goodeidae) under controlled conditions. J Exp Biol Agric Sci. 2016; 4(2):180–93. Available from: https://goodeidworkinggroup.com/sites/default/files/2016-04.pdf
Available from: https://goodeidworkinggr...
) it was encountered in remarkably low abundance only in spring-fed and drainage confluence sites.

The other five species we found in our surveyed sites are widely recognized as invasive in the Central Mexican Plateau (Miller et al., 2009Miller RR, Minckley WL, Norris SM, Gach MH. Peces dulceacuícolas de México. Tlalpan, México, D.F: Comisión Nacional para el Conocimiento y Uso de la Biodiversidad Sociedad Ictiológica Mexicana El Colegio de la Frontera Sur Desert Fishes Council; 2009. ). In all sites, the most dominant species was an invasive poecilid, the specific species varied: P. bimaculatus in dam spillway site, P. mexicana in spring-fed site, and P. reticulata in drainage confluence site. Our data highlights the prevalence of invasive species, constituting 99.4% of the total fish population, posing a significant threat to native fish populations. The presence and abundance of invasive species are of concern because where poeciliids are established, they tend to disperse and colonize new areas naturally (Gomez-Márquez et al., 2016Gómez-Márquez JL, Peña-Mendoza B, Guzmán-Santiago JL. Reproductive biology of Poecilia sphenops Valenciennes, 1846 (Cyprinidontiformes: Poeciliidae) at the Emiliano Zapata reservoir in Morelos, Mexico. Neotrop Ichthyol. 2016; 14(2):e140127. https://doi.org/10.1590/1982-0224-20140127
https://doi.org/10.1590/1982-0224-201401...
). As poeciliids can achieve a high level of invasiveness because they are viviparous fish with short reproductive cycles and high fecundity (Ramírez-García et al., 2017Ramírez-García A, Ramírez-Herrejón JP, Medina-Nava M, Hernández-Morales R, Domínguez-Domínguez O. Reproductive biology of the invasive species Pseudoxiphophorus bimaculatus and Poecilia sphenops in the Teuchitlán River, México. J Appl Ichthyol. 2017; 34(1):81–90. https://doi.org/10.1111/jai.13543
https://doi.org/10.1111/jai.13543...
). These findings are of concern as invasive species represents one of the most severe and less controlled problems around the country (Contreras-MacBeath et al., 2014Contreras-MacBeath T, Rodríguez MB, Sorani V, Goldspink C, Reid GM. Richness and endemism of the freshwater fishes of Mexico. J Threat Taxa. 2014; 6(2):5421–33. https://doi.org/10.11609/JoTT.o3633.5421-33
https://doi.org/10.11609/JoTT.o3633.5421...
).

In the Tula River, twospot livebearers (P. bimaculatus) dominated the dam spillway site where the species richness was relatively low and only other invasive species were present. This is an invasive species widely spread throughout freshwater ecosystems in central Mexico that can tolerate harsh environmental conditions and could establish widely around the globe (Gomez-Maldonado et al., 2023Gomez-Maldonado S, Calleros A, Salazar-Rueda I, Camacho-Cervantes M. The invasive twospot livebearer’s biology, its current and potential global distribution. J. Fish Biol. 2023; 103(5):854–63. https://doi.org/10.1111/jfb.15483
https://doi.org/10.1111/jfb.15483...
). Mature females and males of P. bimaculatus have been found in degraded sites of rivers where they tend to spread and colonize new areas (Ramírez-García et al., 2017Ramírez-García A, Ramírez-Herrejón JP, Medina-Nava M, Hernández-Morales R, Domínguez-Domínguez O. Reproductive biology of the invasive species Pseudoxiphophorus bimaculatus and Poecilia sphenops in the Teuchitlán River, México. J Appl Ichthyol. 2017; 34(1):81–90. https://doi.org/10.1111/jai.13543
https://doi.org/10.1111/jai.13543...
). Furthermore, this species can endure changes in the elements of the trophic web and food availability, as it can feed from terrestrial insects, fish eggs, and fish larvae, therefore it can threaten native fish populations (Carbajal-Becerra et al., 2020Carbajal-Becerra O, Olvera-Rodríguez KJ, Souza GM, Durán-Rodríguez OY, Ramírez-García A, Ramírez-Herrejón JP. Trophic strategies of the invasive Twospot livebearer (Pseudoxiphophorus bimaculatus, Teleostei: Poeciliidae) in a gradient of environmental quality in central Mexico. Neotrop Ichthyol. 2020; 18(2):e190080. https://doi.org/10.1590/1982-0224-2019-0080
https://doi.org/10.1590/1982-0224-2019-0...
). For instance, in other basins from central Mexico P. bimaculatus was classified as a threat to N. calientis populations through egg predation (Carbajal-Becerra et al., 2020Carbajal-Becerra O, Olvera-Rodríguez KJ, Souza GM, Durán-Rodríguez OY, Ramírez-García A, Ramírez-Herrejón JP. Trophic strategies of the invasive Twospot livebearer (Pseudoxiphophorus bimaculatus, Teleostei: Poeciliidae) in a gradient of environmental quality in central Mexico. Neotrop Ichthyol. 2020; 18(2):e190080. https://doi.org/10.1590/1982-0224-2019-0080
https://doi.org/10.1590/1982-0224-2019-0...
).

Drainage confluence site stands out as a significant site, the prevalence of P. reticulata at this site is particularly striking, with a notably higher abundance of this species than observed at other sites, linked to river velocity and higher pH levels. Additionally, drainage confluence site is situated within an urban perimeter and is impacted by anthropogenic influences, especially after the incorporation of the Salado River. Guppies’ high dominance is not surprising, given that guppies are known for being successful invaders (Magurran, 2005Magurran AE, Ramnarine IW. Evolution of mate discrimination in a fish. Curr Biol. 2005; 15(21):867–68. https://doi.org/10.1016/j.cub.2005.10.034
https://doi.org/10.1016/j.cub.2005.10.03...
). They can establish populations in a wide range of conditions (Gibson, Hirst, 1955Gibson MB, Hirst B. The effect of salinity and temperature on the pre-adult growth of guppies. Copeia. 1955; 1955(3):241–43. https://doi.org/10.2307/1440474
https://doi.org/10.2307/1440474...
; Chervinski, 1984Chervinski J. Salinity tolerance of the guppy, Poecilia reticulata Peters. J Fish Biol. 1984; 24(4):449–52. https://doi.org/10.1111/j.1095-8649.1984.tb04815.x
https://doi.org/10.1111/j.1095-8649.1984...
; Chung, 2001Chung KS. Critical thermal maxima and acclimation rate of the tropical guppy Poecilla reticulata. Hydrobiologia. 2001; 462:253–57. https://doi.org/10.1023/A:1013158904036
https://doi.org/10.1023/A:1013158904036...
), manage to survive and settle in changing temperatures (Chung, 2001Chung KS. Critical thermal maxima and acclimation rate of the tropical guppy Poecilla reticulata. Hydrobiologia. 2001; 462:253–57. https://doi.org/10.1023/A:1013158904036
https://doi.org/10.1023/A:1013158904036...
; Reeve et al., 2014Reeve AJ, Ojanguren AF, Deacon AE, Shimadzu H, Ramnarine IW, Magurran AE. Interplay of temperature and light influences wild guppy (Poecilia reticulata) daily reproductive activity. Biol J Linn Soc Lond. 2014; 111(3):511–20. https://doi.org/10.1111/bij.12217
https://doi.org/10.1111/bij.12217...
) and salinities (Chervinski, 1984Chervinski J. Salinity tolerance of the guppy, Poecilia reticulata Peters. J Fish Biol. 1984; 24(4):449–52. https://doi.org/10.1111/j.1095-8649.1984.tb04815.x
https://doi.org/10.1111/j.1095-8649.1984...
), which may be vastly different from those of their native environment. The species composition observed in our study aligns with the findings of Gutierrez-Yurrita (2013). However, they reported P. reticulata a new record for the basin, and it was only present in the middle section of the Moctezuma River, and not in the Tula River. In contrast, we found P. reticulata in all three sites and was dominant in drainage confluence, suggesting that the species has expanded its territory in recent years. P. reticulata is a very social species that derives benefits from associations with natives (Camacho-Cervantes et al., 2015Camacho-Cervantes M, Ojanguren AF, Magurran AE. Exploratory behaviour and transmission of information between the invasive guppy and native Mexican topminnows. Anim Behav. 2015; 106:115–20. https://doi.org/10.1016/j.anbehav.2015.05.012
https://doi.org/10.1016/j.anbehav.2015.0...
) and other poeciliid invaders (Santiago-Arellano et al., 2021Santiago-Arellano A, Palomera-Hernandez V, Camacho-Cervantes M. Con- and heterospecific shoaling makes invasive guppies more risk taking. Front Ecol Evol. 2021; 9:624245. https://doi.org/10.3389/fevo.2021.624245
https://doi.org/10.3389/fevo.2021.624245...
), such as transmission of information and foraging efficiency or boldness increase. If this were a trend also for the other species found, we hypothesize that twospot and porthole livebearers could also be gaining benefits from associating with natives (Camacho-Cervantes et al., 2023Camacho-Cervantes M, Keller RP, Vilà M. Could non-native species boost their chances of invasion success by socializing with natives? Philos Trans R Soc Lond B Biol Sci. 2023; 378:20220106. https://doi.org/10.1098/rstb.2022.0106
https://doi.org/10.1098/rstb.2022.0106...
) as well as following an invasive meltdown trend, thus increasing the likelihood of exotic species becoming successful when establishing in an already invaded ecosystem (Simberloff, 2006Simberloff D. Invasional meltdown 6 years later: important phenomenon, unfortunate metaphor, or both? Ecol Lett. 2006; 9(8):912–19. https://doi.org/10.1111/j.1461-0248.2006.00939.x
https://doi.org/10.1111/j.1461-0248.2006...
; Green et al., 2011Green PT, O’Dowd DJ, Abbott KL, Jeffery M, Retallick K, Mac Nally R. Invasional meltdown: Invader–invader mutualism facilitates a secondary invasion. Ecology. 2011; 92(9):1758–68. https://doi.org/10.1890/11-0050.1
https://doi.org/10.1890/11-0050.1...
). However, the geometry of propagule pressure can also play a role (Cassey et al., 2018Cassey P, Delean S, Lockwood JL, Sadowski JS, Blackburn TM. Dissecting the null model for biological invasions: a meta-analysis of the propagule pressure effect. PLoS Biol. 2018; 16(4):e2005987. https://doi.org/10.1371/journal.pbio.2005987
https://doi.org/10.1371/journal.pbio.200...
). Unfortunately, there is no available record of the succession of species invasion in the river.

Spring-fed site presented the highest richness and diversity, indicating a relatively even distribution of abundance. In this site, P. mexicana was the most abundant species. Notably, this site was the only site where all seven species were recorded. This may be due to the presence of water springs in the nearby area, which may improve water quality, potentially impacting community structure. Additionally, it is the only site where both native species were present, this may suggest that water springs could positively influence the community structure. For example, in another freshwater site with water springs in the center of Mexico, La Mintzita, the fish community includes 13 fish species, of which four are exotic (Marín-Togo, Blanco-García, 2009Marín-Togo MC, Blanco-García A. Ficha informativa de los humedales de Ramsar, La Mintzita. Ramsar; 2009. ).

The differences observed in the community structure of fish suggest that environmental factors are affecting fish populations in the Tula River. Ecosystem alteration can facilitate the establishment of invasive species and these species, in turn, can impact water quality, generating a synergistic effect on native species populations (Reeve et al., 2014Reeve AJ, Ojanguren AF, Deacon AE, Shimadzu H, Ramnarine IW, Magurran AE. Interplay of temperature and light influences wild guppy (Poecilia reticulata) daily reproductive activity. Biol J Linn Soc Lond. 2014; 111(3):511–20. https://doi.org/10.1111/bij.12217
https://doi.org/10.1111/bij.12217...
). The observation of different invasive poeciliid species dominating at various sites is intriguing and suggests that several factors may contribute to their distribution patterns. These species likely exhibit distinct habitat preferences and environmental tolerances. For instance, P. reticulata appears to be associated with higher pH and river velocity, while P. bimaculatus and P. gracilis were related to lower pH and colder temperatures, and P. mexicana was associated with higher temperatures and lower river velocity. Differences in species dominance further underscore the potential impact of competitive interactions among poeciliids. To understand the mechanisms behind these trends, further investigation is necessary. This may involve conducting additional field surveys to study the ecological conditions and resource availability at each site, as well as performing controlled laboratory experiments to assess the competitive interactions between different poeciliid species.

Our results indicate a clear relationship between river characteristics and fish community structure, highlighting the significance of river width, river velocity, temperature, dissolved oxygen, and pH. Specifically, we found that wider rivers tend to host higher species diversity this may be due to the availability of diverse habitats and microhabitats that can support a variety of species with different ecological niches (Ramírez et al., 2022Ramírez C, Barba R, Caspeta JM, Córdova F, Espinosa E, Larre S et al. Aquatic biota of the middle basin of the Lacantún River, Chiapas and the importance of long-term monitoring. Rev Mex Biodivers. 2022; 93:e934844. https://doi.org/10.22201/ib.20078706e.2022.93.4844
https://doi.org/10.22201/ib.20078706e.20...
). River velocity and pH demonstrated significant correlations with the abundance of individuals, particularly seem to be favoring P. reticulata, which dominated the drainage confluence site consistently across all seasons. Additionally, our analysis indicates a significant positive relationship between temperature and species richness. However, it is crucial to acknowledge the influence of other factors like habitat complexity and nutrient availability, which are commonly linked to warmer environments (Caissie, 2006Caissie D. The thermal regime of rivers: a review. Freshw Biol. 2006; 51(8):1389–406. https://doi.org/10.1111/j.1365-2427.2006.01597.x
https://doi.org/10.1111/j.1365-2427.2006...
). Furthermore, the significant negative relationship between temperature and dissolved oxygen is consistent with the widely recognized phenomenon that warmer water holds less dissolved oxygen, potentially leading to stress for aquatic organisms (Córdova-Tapia et al., 2018Córdova-Tapia F, Hernández-Marroquín V, Zambrano L. The role of environmental filtering in the functional structure of fish communities in tropical wetlands. Ecol Freshw Fish. 2018; 27(2):522–32. https://doi.org/10.1111/eff.12366
https://doi.org/10.1111/eff.12366...
). This finding holds particular significance in the context of climate change and the anthropogenic impacts on aquatic ecosystems (Daufresne, Boet, 2007Daufresne M, Boet P. Climate change impacts on structure and diversity of fish communities in rivers. Glob Change Biol. 2007; 13(12):2467–78. ).

Achieving a comprehensive understanding of water quality necessitates a more specific and in-depth study, involving the monitoring of a broader array of water quality parameters at increased frequencies and over extended durations. For instance, within this particular system, we observed greater spatial than temporal variation in species composition, which can be attributed to anthropogenic alterations. Conducting a study of this nature can be highly complex due to the diverse range of biological, chemical, and physical factors that interact in the river. As such, it is crucial to consider the presence of heavy metals, residues from petroleum refining industry, pharmaceutical products, pesticides, and other emerging contaminants that may affect the community structure (Ortiz-Gallarza, Ramirez-Lopez, 2003Ortiz-Gallarza SM, Ramírez-López JA. Water quality of the Tula River related to the petroleum refining industry: accumulation factors and treatments. WIT Trans Ecol Environ. 2003; 65:67–77. ; Rubio-Franchini et al., 2016Rubio-Franchini I, López-Hernández M, Ramos-Espinosa MG, Rico-Martínez R. Bioaccumulation of metals arsenic, cadmium, and lead in zooplankton and fishes from the Tula River watershed, Mexico. Water Air Soil Pollut. 2016; 227(5):1–12. https://doi.org/10.1007/s11270-015-2702-1
https://doi.org/10.1007/s11270-015-2702-...
; Díaz, Peña-Alvarez, 2017Díaz A, Peña-Alvarez A. A simple method for the simultaneous determination of pharmaceuticals and personal care products in river sediment by ultrasound-assisted extraction followed by solid-phase microextraction coupled with gas chromatography–mass spectrometry. J Chromatogr Sci. 2017; 55(9):946–53. https://doi.org/10.1093/chromsci/bmx058
https://doi.org/10.1093/chromsci/bmx058...
). Nevertheless, the presence of native species has been documented, making it worthwhile to comprehend the factors driving the success of invasive species and develop sustainable approaches to control their spread and reduce their negative effects.

Invasive species have become crucial in the study of aquatic systems as they frequently outcompete native species, particularly in polluted habitats (Bourret et al., 2008Bourret V, Couture P, Campbell PGC, Bernatchez L. Evolutionary ecotoxicology of wild yellow perch (Perca flavescens) populations chronically exposed to a polymetallic gradient. Aquat Toxicol. 2008; 86(1):76–90. https://doi.org/10.1016/j.aquatox.2007.10.003
https://doi.org/10.1016/j.aquatox.2007.1...
; Gomes-Silva et al., 2020Gomes-Silva G, Pereira BB, Liu K, Chen B, Santos VSV, Menezes GHT et al. Using native and invasive livebearing fishes (Poeciliidae, Teleostei) for the integrated biological assessment of pollution in urban streams. Sci Total Environ. 2020; 698:134336. https://doi.org/10.1016/j.scitotenv.2019.134336
https://doi.org/10.1016/j.scitotenv.2019...
). In this case, the native species in Tula River face a double pressure of anthropogenic alteration and invasion, which can act synergistically (Cazzolla-Gatti, 2016Cazzolla-Gatti R. Freshwater biodiversity: a review of local and global threats. Int J Environ Stud. 2016; 73(6):887–904. https://doi.org/10.1080/00207233.2016.1204133
https://doi.org/10.1080/00207233.2016.12...
; Camacho-Cervantes, Wong, 2023Camacho-Cervantes M, Wong BBM. Invasive species behaviour in a toxic world. Trends Ecol Evol. 2023; 38(11):1024–27. https://doi.org/10.1016/j.tree.2023.07.006
https://doi.org/10.1016/j.tree.2023.07.0...
). The Tula River, despite being highly polluted and invaded, presents a significant opportunity for restoration due to its surroundings and the importance of reusing wastewater from major cities, as has been successfully done in other countries (Bain et al., 2014Bain DJ, Copeland EM, Divers MT, Hecht M, Hopkins KG, Hynicka J et al. Characterizing a major urban stream restoration project: Nine mile run (Pittsburgh, Pennsylvania, USA). J Am Water Resour Assoc. 2014; 50(6):1608–21. https://doi.org/10.1111/jawr.12225
https://doi.org/10.1111/jawr.12225...
).

The rapid loss of species and habitats in the region has raised concerns regarding the need to protect and conserve ecologically important areas and species (Gutiérrez-Yurrita et al., 2013Gutiérrez-Yurrita PJ, Morales-Ortiz JA, Marín-García L. Diversidad biológica, distribución y estrategias de conservación de la ictiofauna de la cuenca del río Moctezuma, Centro de México. Limnetica. 2013; 32(2):215–28. https://doi.org/10.23818/limn.32.18
https://doi.org/10.23818/limn.32.18...
). To address these concerns, a basin ecosystem management scheme can be implemented that coordinates the management of public and private economic resources. The National Strategy on Invasive Species in Mexico is a comprehensive plan established by the Mexican government to address the issue of invasive species management. Its main objective is to prevent the introduction and spread of exotic species that may pose a threat to biodiversity and native ecosystems. To achieve this, the strategy focuses on various actions, such as early identification and risk assessment of potential invasive species, implementation of control and eradication measures when necessary, and strengthening cooperation among government entities, academic institutions, non-governmental organizations, and civil society (Conabio, 2010Comisión Nacional para el Conocimiento y Uso de la Biodiversidad (Conabio). Estrategia Nacional sobre especies invasoras en México, prevención, control y erradicación. Ciudad de México: México; 2010. ). The dominance of invasive species underscores the need for urgent conservation efforts to protect and restore the native fish populations and prevent the arrival of new exotics (Suárez-Rodríguez et al., 2023Suárez-Rodríguez M, del-Val E, Domínguez-Domínguez O, Ojanguren AF, Camacho-Cervantes M. Population growth and behavioural interactions of a critically endangered fish with co-occurring native and exotic species. Freshw Biol. 2023; 68(4):698–710. https://doi.org/10.1111/fwb.14057
https://doi.org/10.1111/fwb.14057...
). We emphasize the importance of implementing measures to control the spread and impact of invasive species, including monitoring and regulation of species introduction and improved management strategies to promote the conservation of native species. Unless immediate and effective action is taken, the dominance of invasive species will continue to threaten native species in the Mexican Central Plateau.

ACKNOWLEDGEMENTS

This research was funded by PAPIIT-DGAPA-UNAM IA202419 and IA201722 grants awarded to MCC. VPH thanks CONACYT for the postgrad scholarship No 675430. Authors thank Dr. J. Jaime Zúñiga-Vega and Dr. Guillermina Alcaraz for insightful comments to discuss our results, Abigail Santiago-Arellano, Sebastian Gomez-Maldonado, and Yannire Vazquez-Benitez for their help to carry out fieldwork, and Ruth Luna Soria and Gabriela Ramos Mayoral for their help during the preparation of the manuscript. FCT thanks the Lost Paragraph Society for essential support.

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ADDITIONAL NOTES

  • HOW TO CITE THIS ARTICLE

    Córdova-Tapia F, Palomera-Hernández V, Camacho-Cervantes M. Invasive poeciliids dominate fish community in a highly altered river: insights from a diversity study of riverbank fishes in Mexico. Neotrop Ichthyol. 2024; 22(1):e230042. https://doi.org/10.1590/1982-0224-2023-0042

Edited-by

Emili Garcia-Berthou

Data availability

Data citations

United Nations (UN). World Urbanization Prospects 2018: Highlights. Department of Economic and Social Affairs, Population Division. 2019.

Publication Dates

  • Publication in this collection
    05 Apr 2024
  • Date of issue
    2024

History

  • Received
    17 Apr 2023
  • Accepted
    21 Jan 2024
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