Open-access Conservation status of the freshwater fish species from Ceará State, Brazil

Abstract

Red Lists, which assess species’ extinction risk, are essential in formulating public policies for natural resources management and impact mitigation. The objective of this study was to characterize the conservation status of the continental ichthyofauna of the State of Ceará, based on ichthyological occurrence data and criteria from the International Union for Conservation of Nature. Eighty-five fish species belonging to 59 genera, 25 families, and eight orders were recorded in Ceará. Forty-three species were considered Least Concern, four Near Threatened, 17 were threatened, 15 were Data Deficient, and six species were not evaluated. Among the 17 species considered threatened, five were classified as Vulnerable, five as Endangered, and seven as Critically Endangered. The Metropolitan and Salgado basins presented the highest richness (44 and 39 species, respectively). In contrast, the Serra de Ibiapaba (6) and Curu (17) basins had the lowest richness, indicating wide variability among the evaluated basins. The basins with the highest relative number of threatened fish species were the Metropolitan, Litoral, and lower Jaguaribe basins. These findings highlight the urgent need for targeted conservation actions to safeguard the freshwater fish diversity in Ceará, particularly in the basins with the highest number of threatened species.

Keywords:
Caatinga fish; Conservation biology; Hydrographic basins; Northeastern Brazil; Red list of threatened fish species

Resumo

Listas vermelhas, que avaliam o risco de extinção das espécies, são fundamentais na formulação de políticas públicas de gestão dos recursos naturais e mitigação de impactos. O objetivo desse estudo foi caracterizar o estado de conservação da ictiofauna continental do estado do Ceará, com dados de ocorrências ictiológicas e critérios da União Internacional para Conservação da Natureza. Oitenta e cinco espécies de peixes pertencentes a 59 gêneros, 25 famílias e oito ordens foram registradas no Ceará. Quarenta e três espécies foram consideradas menos preocupantes, quatro quase ameaçadas, 17 ameaçadas de extinção, 15 com dados insuficientes e seis espécies não foram avaliadas. Dentre as 17 espécies consideradas ameaçadas, cinco foram classificadas como Vulneráveis, cinco Em Perigo e sete Criticamente em Perigo. As bacias Metropolitana e Salgado apresentaram a maior riqueza (44 e 39 espécies, respectivamente), enquanto as bacias da Serra de Ibiapaba (6) e Curu (17) apresentaram as menores riquezas, indicando ampla variabilidade entre as bacias avaliadas. As bacias com maior número de espécies de peixes ameaçadas foram a Metropolitana, Litoral e baixo Jaguaribe. Esses resultados destacam a urgente necessidade de ações de conservação para salvaguardar a diversidade de peixes de água doce do Ceará, particularmente nas bacias com mais espécies ameaçadas.

Palavras chave:
Bacias hidrográficas; Biologia da conservação; Lista vermelha de espécies de peixes ameaçadas; Nordeste do Brasil; Peixes da Caatinga

INTRODUCTION

Assessing the conservation status of species is essential for formulating public policies aimed at natural resource management and impact mitigation. Including freshwater fish as a target group for protection actions is particularly significant for aquatic ecosystems, as these species have rarely been prioritized in establishing conservation measures (see Frederico et al., 2021; Leal et al., 2021). Freshwater fish, in particular, are considered vulnerable and have historically been neglected in the northeastern region of Brazil (Berbel-Filho et al., 2018). The State of Ceará is located within the Mid-Northeastern Caatinga Ecoregion (MNCE), one of the least-known regions in the world regarding ichthyofaunal biodiversity (Berbel-Filho et al., 2018). Nonetheless, this region has important records of fish species (Rosa et al., 2003; Rodrigues-Filho et al., 2016; Lima et al., 2017). A notable increase in studies has challenged the notion that Ceará’s freshwater biodiversity might be underestimated. Information on population characteristics and species distribution in this region is crucial for developing extinction risk assessments or a Red List of Threatened Fish Species of Ceará, a fundamental tool for conservation initiatives.

The “Inventário da Fauna do Ceará” was launched by the “Programa Cientista Chefe”of the Government of the Ceará State (Law 17,378, January 4, 2021), containing 1,275 vertebrate species, including 502 fish species (400 marine and 102 freshwater), 140 mammals (25 marine and 115 continental), 133 reptiles, 57 amphibians, and 443 birds (SEMA, 2022). The list of freshwater fish of Ceará, compiled by Sánchez-Botero et al. (2021), identified 84 native species and 18 introduced. Of the total number of species in the ichthyofauna of Ceará, four were listed as threatened according to the Red List of the Instituto Chico Mendes de Conservação da Biodiversidade (ICMBio). Four were assessed as threatened in the International Union for Conservation of Nature (IUCN) Red List of Threatened Species (hereinafter IUCN Red List). However, the number of freshwater fish species considered threatened with extinction in Ceará may be underestimated.

State-level Red Lists are crucial for more regional assessments, which could foster better local conservation efforts with more specific biases for targeted issues depending on the region of the country. Red lists of threatened species of freshwater fish have been published in the states of Pará (the only one from North Brazil) (COEMA, 2007), Bahia (the only one from Northeast Brazil) (SEMA, 2017; Silva et al., 2020a), Minas Gerais (COPAM, 2010), Espírito Santo (IEMA, 2022), Rio de Janeiro (SEMA, 1998), and São Paulo (SMA, 2018) (Southeast Brazil), Paraná (Paraná, 2018), Santa Catarina (FATMA, 2011), and Rio Grande do Sul (SEMA, 2014) (South Brazil). Thus, most Brazilian states (about 65%) still do not have assessments regarding their threatened fish biodiversity, including the Ceará State.

Regarding the distribution of ichthyofauna in the river basins of Ceará State, it is noteworthy that only the Jaguaribe and Mundaú river basins have comprehensive information on the composition of this faunal group throughout most of their courses (Lima et al., 2017; Teixeira et al., 2017; Rodrigues-Filho et al., 2019; Silva et al., 2020b). The other river basins in the Ceará State (nine in total) have sporadic information on ichthyofauna and lack continuous monitoring, requiring greater sampling efforts to understand their composition. Among the most neglected sections of the state’s river basins in terms of ichthyofauna knowledge are the headwaters and streams. These areas remain poorly studied and are under constant threat from anthropogenic activities such as mining, removal of riparian vegetation, and the perennialization of water flow, among others (Chiu et al., 2017; Sánchez-Botero et al., 2017; Silva et al., 1996; Vorste et al., 2020; Terra et al., 2021).

Currently, there are serious risks to the maintenance of the biodiversity of freshwater fish in the Ceará State, due to projects with significant potential to impact the main river basins: pollution derived from mineral extraction, fragmentation of ecosystems due to dam construction, and the introduction of non-native species from the transposition of the São Francisco River. In light of this reality, the objective of this study is to assess the conservation status of freshwater fish species occurring in Ceará State.

MATERIAL AND METHODS

The continental regions of the State of Ceará, located within the Mid-Northeastern Caatinga Ecoregion (MNCE), comprise intermittent rivers and streams, cave streams, temporary pools, and marginal lagoons that harbor native and non-native ichthyofauna (Lima et al., 2017; Sánchez-Botero et al., 2021; Terra et al., 2021). Furthermore, water use management strategies implemented by the human population in the region have led to the development of anthropogenic features such as reservoirs (Morais, Pinheiro, 2011). The territory is mostly located in the semi-arid northeastern region, but it also includes humid and sub-humid areas where elevated mountain ranges create exception islands (Moro et al., 2015). According to the Companhia de Gestão dos Recursos Hídricos (COGERH, 2022), a total of 12 Hydrographic Regions were defined within the scope of the State Water Resources Policy, linked to the Secretaria dos Recursos Hídricos (SRH). These include the basins of Coreaú, Acaraú, Litoral, Curu, Jaguaribe (which contains the sub-basins of lower Jaguaribe, middle Jaguaribe, upper Jaguaribe, Banabuiú, and Salgado), Metropolitana, Serra da Ibiapaba, and Sertões de Crateús (Fig. 1).

The list of native ichthyofauna in the Ceará State (Sánchez-Botero et al., 2021), available on the Secretaria do Meio Ambiente e Mudança do Clima (SEMA) website, was updated based on a review of the literature on the composition of freshwater fish species in the Mid-Northeastern Caatinga Ecoregion (MNCE), and records from the ichthyological collections of the Universidade Federal do Rio Grande do Norte (UFRN) and Universidade Federal da Paraíba (UFPB) and queries on SpeciesLink network (CRIA, 2024). Other institutions follow Sabaj (2020). The database of the ichthyofauna composition and occurrences gathered from the literature review was based on publications in taxonomy, ecology, biogeography, and ethnoichthyology from the following basins: Acaraú (Gurgel-Lourenço et al., 2013, 2015; Batista et al., 2016; Faustino, Terra, 2019; Oliveira et al., 2023; Mapurunga et al., 2024; Oliveira et al., 2024), Coreaú (Rodrigues-Filho et al., 2016, 2018a; Gurgel-Lourenço et al., 2017; Sánchez-Botero et al., 2017; Faustino, Terra, 2019), Curu (Silva et al., 2005; Bezerra et al., 2013; Manna et al., 2017, 2018), lower Jaguaribe (Abrantes et al., 2020; Silva et al., 2020), middle Jaguaribe (Abrantes et al., 2020), upper Jaguaribe (Rodrigues-Filho et al., 2016, 2018b, 2019; Gurgel-Lourenço et al., 2017; Berbel-Filho et al., 2018; Silva et al., 2020; Ramos et al., 2020), Banabuiú (Abrantes et al., 2020), Salgado (Rodrigues-Filho et al., 2016; Gurgel-Lourenço et al., 2017), Litoral (Teixeira et al., 2017; Berbel-Filho et al., 2018; Faustino, Terra, 2019; Abrantes et al., 2020; Gonçalves-Silva et al., 2022), Metropolitana (Rosa, Groth, 2004; Chaves et al., 2013; Sánchez-Botero et al., 2014a; Bezerra et al., 2017; Berbel-Filho et al., 2018; Abrantes et al., 2020, 2023), Sertões de Crateús (Rodrigues-Filho et al., 2016; Berbel-Filho et al., 2018), and Serra da Ibiapaba (Sánchez-Botero et al., 2014b; Rodrigues-Filho et al., 2016; Gurgel-Lourenço et al., 2017).

FIGURE 1 |
Location of the hydrographic basins of the Ceará State, Brazil.

Based on geographic distribution information, we calculated each species’ Extent of Occurrence (EOO; the area contained within the shortest continuous imaginary boundary, which can be drawn to encompass all the points of occurrence of a species) and Area of Occupancy (AOO; a scaled metric that represents the area of suitable habitat currently occupied by the taxon) (IUCN, 2024). Information regarding the classification of ichthyofauna concerning endemism in the Caatinga and MNCE was sourced from Rosa et al. (2003), Gurgel-Lourenço et al. (2013), Ramos et al. (2014), Rodrigues-Filho et al. (2016), Bezerra et al. (2017), Lima et al. (2017), Berbel-Filho et al. (2018), Silva et al. (2020), Abrantes et al. (2020, 2023), and Lustosa-Costa et al.(2024).

Following IUCN recommendations for freshwater fish species, the Minimum Convex Polygon (MCP) was used to calculate the Extent of Occurrence (EOO), encompassing all occurrence points of the species (Brazil; IUCN, 2024). The information indicates whether EOO is < 20,000 km2, < 5,000 km2, or < 100 km2 for each species. It also assesses the conditions of the Area of Occupancy (AOO), determining the qualitative degree of fragmentation and the number of locations where the fish species is found. It notes if there is a continued decline in EOO and/or AOO, in addition to habitat quality conditions and/or number of mature individuals, where available. AOO is noted if it is < 2,000 km2, < 500 km2, or < 10 km2. The thresholds of EOO and AOO areas assessed here were used, along with other criteria, to assess the species’ extinction risk and, when applicable, categorize them as Vulnerable, Endangered, and Critically Endangered (IUCN, 2024).

Occurrence points registered in Ceará State, AOO, and EOO were obtained for each species. Calculation of AOO and EOO values in km2 was performed using QGIS software (QGIS, 2024). Concurrently, maps of species richness and the percentage of threatened species per basin in Ceará were developed based on ichthyofauna occurrence data.

To complement occurrence data for fish not documented in scientific literature, historical documents from the Departamento Nacional de Obras Contra as Secas (DNOCS) (Ihering, 1933; Menezes, 1956; DNOCS, 1963; Peixoto, Gurgel, 1978; Gurgel, 1979), Environmental Impact Studies and Environmental Impact Reports provided by the Superintendência Estadual de Meio Ambiente (SEMACE), and the Instituto Brasileiro do Meio Ambiente e Recursos Naturais Renováveis (IBAMA) were consulted.

Set of information related to the number of occurrences of fish species recorded in the basins of Ceará, AOO, and EOO, spatial distribution, population characteristics, occurrence habitats, potential threats, as well as information regarding their conservation status in global (IUCN) and national (ICMBio) red lists, were applied the criteria and categories of the IUCN Red List. This has resulted in the unprecedented determination of extinction risk for continental fish species in the state.

RESULTS

A total of 1,423 records from ichthyological collections with geographic coordinates of species distributed in Ceará State were evaluated. Based on available literature and collection records, 85 species of native fish were recorded across twelve continental basins in Ceará State, with 43 (51%) being endemic to the Caatinga, according to Lima et al. (2017) (Tab. 1). Characiformes accounted for 47% (40) and Siluriformes for 32% (27) of the species; the remaining six orders comprised approximately 20%. Regarding families, Loricariidae represented 15% (13), Acestrorhamphidae 13% (11), and Rivulidae 8% (7) of the species; other families constituted 64%.

A total of 25 species (29%) had localized records, occurring in only one hydrographic basin. Another 42 species (49%) had a wide distribution, occurring in at least three hydrographic basins (Tab. 1). Three species (Erythrinus erythrinus (Bloch & Schneider, 1801), Curimatella lepidura (Eigenmann & Eigenmann, 1889), Gymnotus carapo Linnaeus, 1758) lacked information about their hydrographic basins in the ichthyological collection records, only noting their occurrence in the Ceará State. Six species (7%) had some taxonomic issues: Hemiodus parnaguae Eigenmann & Henn, 1916, Parotocinclus jumbo Britski & Garavello, 2002, Pimelodella witmeri Fowler, 1941, P. wolfi (Fowler, 1941), Pseudancistrus papariae Fowler, 1941 and Trachelyopterus cratensis (Miranda Ribeiro, 1937).

Of the 85 species assessed, 43 were classified as Least Concern (LC), four species as Near Threatened (NT), 17 species were considered threatened under one of the categories (Vulnerable - VU, Endangered - EN, or Critically Endangered - CR), and 15 species having insufficient data to be assessed (Data Deficient - DD). Among the 17 species classified as threatened, four species were categorized as VU B1ab(iii); three species as EN B1ab(iii), three species as CR B1ab(iii), two species as CR B1B2ab(iii), one species as CR A2cde, one species as EN B2ab(iii), one species as CR B2ab(i, ii, iii, iv), one species as VU A2A4ce+B1ab(i,iii), and one species as ENB1ab(iii)+2ab(iii) (Fig. 2; Tab. 2; S1).

TABLE 1 |
Species occurrence by basin, voucher numbers. AC = Acaraú, UJ = upper Jaguaribe, MJ = middle Jaguaribe, LJ = lower Jaguaribe, BA = Banabuiú, CO = Coreaú, CU = Curu, LI = Litoral, ME = Metropolitana, AS = Salgado, SI = Serra da Ibiapaba, SC = Sertões de Crateús.

Additionally, six species were categorized as Not Evaluated (NE) because they were classified as inquirenda based on Lima et al. (2017) and/or Berbel-Filho et al. (2018): Trachelyopterus cratensis, Pimelodella witmeri, Pimelodella wolfi, Aphanotorulus gomesi (Fowler, 1942), Pseudancistrus papariae .

We observed a considerable variability in the number of species among basins (mean 25.1 ± 10.3). The Metropolitana and Salgado basins exhibited the highest species richness (44 and 39 species, respectively). The Serra de Ibiapaba and Curu basins showed the lowest richness (6 and 17 species, respectively) (Fig. 3A). The basins with the highest percentage of threatened fish species were Metropolitana (15.9%), Litoral (14.3%) and lower Jaguaribe (10.5%) (Fig. 3B).

FIGURE 2 |
Number of freshwater fish species in the Ceará State and categories based on IUCN criteria. Legend: LC - Least Concern; DD - Data Deficient; NT - Near Threatened; NE - Not Evaluated; VU - Vulnerable; EN - Endangered; CR - Critically Endangered. The meanings of the codes are detailed in S1.
TABLE 2 |
Conservation status of freshwater fish species in Ceará State. Taxonomic sequence according to Fricke et al. (2024). OCC = Occurrence Coordinates; AOO = Area of Occupancy; EOO = Extent of Occurrence; LC = Least Concern; NT = Near Threatened; CR = Critically Endangered; EN = Endangered; VU = Vulnerable; DD = Data deficient; NE = Not Evaluated. *Species exclusive to Ceará.
FIGURE 3 |
Freshwater fish by hydrographic basin in the Ceará State. A. Species richness; B. Percentage of threatened species.

DISCUSSION

Previous records available from federal agencies regarding the freshwater fish fauna occurring in the Ceará State primarily indicated the use of freshwater fish for human consumption, eradication of species considered ‘pests’ (e.g., piranhas), and stocking activities with both native and non-native species (Ihering, 1933; Menezes, 1956; DNOCS, 1963; Peixoto, Gurgel, 1978, 1979). These documents do not properly include cataloged lists of native fish species in collections nor report actions for the conservation of native freshwater fish. From an academic perspective, the earliest records of native ichthyofauna in Ceará’s freshwater environments (Ihering, 1907; Fowler, 1915) indicated the faunistic influence of the Atlantic Forest and Amazon biomes on the current species composition and distribution. More recently, taxonomic and phylogeographic studies discussed the influences of these biomes and geomorphological processes that have shaped the current freshwater fish diversity (Rosa et al., 2003; Rosa, Groth, 2004; Berbel-Filho et al., 2015; Lima et al., 2017; Rodrigues-Filho et al., 2018a).

Out of the 85 fish species in Ceará State, four are listed in the ICMBio Red List of Threatened Fauna (MMA, 2022) and four are listed in the IUCN Red List. Anablepsoides cearensis (Costa & Vono, 2009), Hypsolebias longignatus (Costa, 2008), and Parotocinclus spilurus (Fowler, 1941) are listed in both lists. Apareiodon davisi (Fowler, 1941) and Hypsolebias martinsi Britzke, Nielsen & Oliveira, 2016 are exclusively listed in the ICMBio and IUCN lists, respectively. Six species were categorized as DD (Data Deficient) by ICMBio and seven by the IUCN Red List. Two species were not assessed by ICMBio (Hemigrammus rodwayi Durbin, 1909 and Hypsolebias gongobira (Abrantes, Ramos, Bento & Lima, 2023), and 31 species were not evaluated by the IUCN Red List. These results highlight a significant number of fish species not evaluated by the IUCN Red List (36%), underscoring the need for updating both national and global official lists.

The high endemism recorded (51%) indicated that almost half of the continental fish species have restricted geographic distribution to the Caatinga (Lima et al., 2017), with eight exclusive to Ceará State: A. cearensis, Hypsolebias antenori (Tulipano, 1973), H. longignatus, H. gongobira, Parotocinclus spilurus, Aspidoras carvalhoi (Nijssen & Isbrücker, 1976), Aspidoras rochai Ihering, 1907, and Hypostomus sertanejo Zawadzki, Ramos & Sabaj, 2017. On the other hand, about one-third of the native fish species in the state are widely distributed, with greater survival potential in the face of natural and anthropogenic disturbances occurring in Ceará’s hydrographic basins. Conversely, the three species without records in the state’s basins highlight the lack of information related to Area of Occupancy (AOO), Extent of Occurrence (EOO), and their actual distributions, indicating the need for further studies. It is noteworthy that some widely distributed species may represent species complexes, with some potentially endemic to Ceará’s basins (e.g., Parotocinclus Eigenmann & Eigenmann, 1889), and others purportedly endemic (e.g., Hypostomus, Pseudancistrus Bleeker, 1862, and Pimelodella Eigenmann & Eigenmann, 1888) (Lima et al., 2017; Berbel-Filho et al., 2018). These taxonomically undefined species underscore the need for further taxonomic and molecular studies to resolve uncertainties, as in the recent study by Lustosa-Costa et al. (2024), which clarifies the species complex of Hypostomus pusarum (Starks, 1913) using integrative taxonomy. Indeed, Lima et al. (2017), Berbel-Filho et al. (2018), and Terra et al. (2021) highlight the need for more studies on Caatinga ichthyofauna to understand biological aspects.

Among the 17 threatened continental fish species in the State of Ceará, the order Cyprinodontiformes stands out with seven species, followed by Siluriformes with six species and Characiformes with four species. Rivulidae and Loricariidae include six and three species, respectively, classified under some threat criteria. These species are predominantly small-sized and exhibit restricted geographical distributions. These two characteristics are correlated (Ripple et al., 2017) and have been considered predictors of extinction risk for freshwater fish species in global assessments (Olden et al., 2007; Kalinkat et al., 2017).

The majority of Rivulidae species (86%) are threatened in Ceará. In Brazil, this family is also among the freshwater fish groups at the highest risk of extinction, with 125 species classified under some threat level (Castro, Polaz, 2019). In addition to the intrinsic characteristics mentioned above, another critical factor for this group is habitat integrity. Most species within this family exhibit adaptations and seasonal life cycles that enable survival under the extreme environmental conditions of temporary pools (Berois et al., 2016). However, such habitats are often overlooked by conservation initiatives (Zacharias, Zamparas, 2010; Calhoun et al., 2017) and are increasingly threatened by various anthropogenic impacts, including road construction, agriculture, and sand extraction for the construction industry (Abrantes et al., 2020). This finding underscores the urgent need to implement protection policies for this group in the State, ensuring the preservation of permanent wetlands and seasonal pools in floodplain areas where they complete their life cycles (Teixeira et al., 2017; Abrantes et al., 2020).

The Metropolitana, Litoral, and lower Jaguaribe basins exhibit a higher percentage of threatened fish species (seven, four, and two species, respectively). This result possibly reflects the regional occupation pattern, which concentrates on activities such as industry and tourism along the coastal region (Pinheiro et al., 2016). Particularly in the Metropolitan Region, another impact source to be considered is urbanization. This factor can contribute to the decline in freshwater fish biodiversity as it is associated with processes such as loss of natural habitats (Walsh et al., 2005), increased pollutants and organic matter (Parr et al., 2016), and the introduction of non-native species (Ortega et al., 2021). The disparity in species richness among these basins, with higher values in the Metropolitana, likely indicates greater sampling effort in areas closer to research institutions. This bias is common in biodiversity data (Costa et al., 2010; Cardoso et al., 2024) and underscores the need to expand sampling efforts to enhance knowledge of fish distribution in the state.

Other state red lists have reported varying numbers of threatened continental fish species, with the states of Pará, Espírito Santo, and Paraná having the lowest numbers (nine, eleven, and fifteen species, respectively), and São Paulo having the highest number (66 species) (COEMA, 2007; Paraná, 2018; SMA, 2018; IEMA, 2022). Rivulidae is prominently represented with a high number of threatened species, being the most represented family in Bahia (14 species), Espírito Santo (three), and Rio Grande do Sul (27 species) (SEMA, 2014; SEMA, 2017; Silva et al., 2020a; IEMA, 2022), and the second most represented family in Minas Gerais (10), Rio de Janeiro (10), and Santa Catarina (seven species) (SEMA, 1998; COPAM, 2010; FATMA, 2011). Loricariidae is represented in the number of threatened species in São Paulo (14) and Minas Gerais (seven species) (COPAM, 2010; SMA 2018). Families not yet recorded in Ceará State, such as Pimelodidae and Trichomycteridae, also comprise relatively high numbers in other state lists (ranging from one to eight species, and one to twelve species, respectively), and potential occurrences in Ceará cannot be ruled out with increased sampling efforts.

The total number of fish species categorized as Least Concern (LC = 43), Data Deficient (DD = 15), Near Threatened (NT = 4), and Not Evaluated (NE = 6) accounts for 80% of the ichthyofauna documented in this study. The fish species classified as LC (51% of the total) are widely distributed across the hydrographic basins of Ceará, indicating no imminent threat of extinction. However, considering the historical introduction of non-native species, the construction of large dams impacting underlying ecosystems, and efforts to eradicate species deemed harmful such as piranhas, as documented by historical records from DNOCS, this value underscores a resilient and robust ichthyofauna. On the other hand, the aforementioned disturbances may have led to the extinction of species of fish that were never formally recorded.

The 15 fish species categorized as Data Deficient (DD) were justified in this category due to limited available information on population aspects, distribution, and taxonomic issues. Part of the species in this category (Erythrinus erythrinus (Bloch & Schneider, 1801), Curimatella lepidura (Eigenmann & Eigenmann, 1889), Gymnotuscarapo Linnaeus, 1758, Aphanotorulusgomesi (Fowler, 1942)) do not have occurrence coordinates in the basins of Ceará, although their presence is known from other bibliographic sources (Rosa et al., 2003; Rosa, Groth, 2004; Silva et al., 2005, 2020b; Rodrigues-Filho et al., 2016; Berbel-Filho et al., 2018; Sánchez-Botero et al., 2021). Five species also classified in this category have only one occurrence coordinate (Sternopygusmacrurus (Bloch & Schneider, 1801), Platydorasbrachylecis Piorski, Garavello, Arce H. & Sabaj Pérez, 2008, Ancistrusdamasceni (Steindachner, 1907), Pterygoplichthysparnaibae (Weber, 1991) and Metynnis lippincottianus (Cope, 1870) or only two (Ctenobryconspilurus (Valenciennes, 1850), Megalamphodus bentosi (Durbin, 1908) and Kryptolebias hermaphroditus Costa, 2011). Therefore, greater collection efforts for these species are necessary to assess their conservation status and potential extinction threats. In addition to this, six other species have dubious taxonomy Hyphessobrycon piabinhas Fowler, 1941, Trachelyopterus cratensis, Pimelodella witmeri, P. wolfi, Aphanotorulus gomesi, and Pseudancistrus papariae.

Large-scale developments underway in Ceará State are likely to cause disturbances that will affect freshwater fish fauna. The Complexo Industrial e Portuário do Pecém (CIPP), through a public utility decree defining its coverage area (CEARÁ, 2007), plans development projects in areas containing stream springs as well as the infilling of lakes and lagoons, impacting local biodiversity (Meireles et al., 2012). The species Hemigrammus guyanensis Géry, 1959 and Anablepsoides cearensis, which occur in the CIPP region, are classified as threatened with extinction according to the assessment conducted in this study, with the latter having a restricted distribution (AOO <10 km2). Furthermore, the São Francisco River Transposition Project expected effects include the introduction of non-native species, potentially altering biotic interactions (competition, predation, and parasitism) and modifying natural habitats, thereby impacting native species (Silva et al., 2020b; Falkenberg et al., 2024). These disturbances are expected to particularly impact the threatened ichthyofauna found in the Jaguaribe River sub-basins, including Apareiodon davisi, Cynolebias microphthalmus Costa & Brasil, 1995, Hypsolebias antenori, Parotocinclus spilurus, and Pimelodella dorseyi Fowler, 1941. In addition to the aforementioned ongoing projects, other initiatives of concern to be considered in the medium- and long-term conservation strategies for freshwater fish in the State are the ongoing uranium and phosphate mining projects in the municipality of Santa Quitéria, in the licensing phase (EIA, 2021).

In the State of Ceará, dam construction has historically been adopted as a strategy to ensure water supply for the human population, addressing water scarcity and prolonged droughts typical of the semi-arid region (Gurgel-Lourenço et al., 2023). These structures are also crucial for providing water for livestock and supporting agricultural activities (Gaiser et al., 2003). However, such developments fragment riverine habitats, preventing species from moving between breeding, growth, and feeding areas, leading to population declines or even local extinctions (Barbarossa et al., 2020; Sun et al., 2023). Dams represent one of the main threats to migratory fish species, which rely on the natural flow of rivers to complete their life cycles (Thomé et al., 2005), leading to the reduction or extinction of populations, as observed in the case of Salminus hilarii (Valenciennes,1849) in the Jaguaribe River basin (in Ceará State, it occurs exclusively in this basin), a migratory species that was once among the most important fisheries resources, is now absent and possibly extinct (Menezes, 1953; Lima, 2022). The construction of new dams exacerbates conservation risks for this fauna, particularly for many migratory species, such as those from the genera Prochilodus Agassiz, 1829 and Leporinus Agassiz, 1829, which have traditionally been targeted by artisanal fishing in Ceará State (Batista et al., 2016; Costa et al., 2016). Additionally, Hemiodus parnaguae and Prochilodus lacustris Steindachner, 1907, classified as near-threatened and recorded in the State only within the Sertões de Crateús basin, could be negatively impacted by the ongoing construction of the Fronteiras Dam in Crateús-CE. Thus, implementing technologies such as fish ladders and waterways should increasingly be promoted and adopted as a mitigation strategy (Kemp, 2015), still with risks regarding how effective they can be for all fish species.

In conclusion, this study underscores the urgent need to implement impact mitigation programs for freshwater fish in Ceará. The species distribution information provided in this study should be considered and applied to assist in defining and prioritizing protected areas and management measures to ensure ichthyofauna biodiversity maintenance and protection of species facing some threat level. These areas should encompass hydrographic basins that shelter threatened fish species and exhibit higher species richness. This study provides a survey of information on the conservation status of the continental ichthyofauna of the Ceará State. However, the extinction risk assessment proposals presented here must undergo procedures established by the State to meet legal requirements and officially become the Red List of the State of Ceará.

ACKNOWLEDGEMENTS

The authors would like to thank the Universidade Federal do Ceará (UFC), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for financial support through the MCTI/CNPq Program (Grant 28/2018, 423628/2018–6 and Grant 63/2022, 409354/2022–8) for the field and scholarship support to RCGL and LMP. We thank the Programa de Pós-Graduação em Sistemática, Uso e Conservação da Biodiversidade - PPGSIS/UFC for support to MCFG during magister research. We are grateful for the support of Instituto Nacional de Ciência e Tecnologia de Materiais na Interface Continente-Oceano (INCT-TMCOcean), based at UFC. SMQL thanks the CNPq for the productivity Grant (312066/2021–0). TPAR thanks the CNPq for the PDS grant (102460/2022–1). PC acknowledges the visiting researcher grant from FUNCAP (PVS–0215–00123.2.00/23) and a Save Our Seas Foundation Conservation Fellowship (SOSF 588).

REFERENCES

  • Abrantes YG, Medeiros LS, Bennemann ABA, Bento DM, Teixeira FK, Rezende CF et al. Geographic distribution and conservation of seasonal killifishes (Cyprinodontiformes, Rivulidae) from the Mid-Northeastern Caatinga ecoregion, northeastern Brazil. Neotrop Biol Conserv. 2020; 15(3):301–15. https://doi.org/10.3897/neotropical.15.e51738
    » https://doi.org/10.3897/neotropical.15.e51738
  • Abrantes YG, Ramos TPA, Bento DM, Lima SMQ. Molecular delimitation of the seasonal killifishes of the Hypsolebias antenori species group (Cyprinodontiformes, Rivulidae), with description of two new species from the Caatinga coastal basins, northeastern Brazil. Zootaxa. 2023; 5389(5):545–62. https://doi.org/10.11646/zootaxa.5389.5.2
    » https://doi.org/10.11646/zootaxa.5389.5.2
  • Barbarossa V, Schmitt RJP, Huijbregts MAJ, Zarfl C, King H, Schipper AM. Impacts of current and future large dams on the geographic range connectivity of freshwater fish worldwide. PNAS. 2020; 117(7):3648–55. https://doi.org/10.1073/pnas.1912776117
    » https://doi.org/10.1073/pnas.1912776117
  • Batista LPP, Sánchez-Botero JI, Paula EO, Silva EV. Etnotaxonomia e tabus alimentares dos pescadores artesanais nos açudes Araras e Edson Queiroz, bacia do Rio Acaraú, Ceará, Brasil. Entorno Geográfico. 2016; 12:34–49. https://doi.org/10.25100/eg.v0i12.3543
    » https://doi.org/10.25100/eg.v0i12.3543
  • Berbel-Filho WM, Martinez PA, Ramos TPA, Torres RA, Lima SMQ. Inter- and intra-basin phenotypic variation in two riverine cichlids from northeastern Brazil: potential eco-evolutionary damages of São Francisco interbasin water transfer. Hydrobiologia. 2015; 766:43–56. https://doi.org/10.1007/s10750-015-2440-9
    » https://doi.org/10.1007/s10750-015-2440-9
  • Berbel-Filho WM, Ramos TPA, Jacobina UP, Maia DJG, Torres RA, Lima SMQ. Updated checklist and DNA barcode-based species delimitations reveal taxonomic uncertainties among freshwater fishes from the mid-north-eastern Caatinga ecoregion, north-eastern Brazil. J Fish Biol. 2018; 93(2):311–23. https://doi.org/10.1111/jfb.13758
    » https://doi.org/10.1111/jfb.13758
  • Berois N, García G, Sá RO. Annual fishes: life history strategy, diversity, and evolution. Boca Raton: CRC Press; 2016.
  • Bezerra LAV, Angelini R, Vitule JRV, Coll M, Sánchez-Botero JI. Food web changes associated with drought and invasive species in a tropical semiarid reservoir. Hydrobiologia. 2017; 817:475–89. https://doi.org/10.1007/s10750-017-3432-8
    » https://doi.org/10.1007/s10750-017-3432-8
  • Bezerra LAV, Gurgel-Lourenço RC, Sánchez-Botero JI. Vertical segregation of Serrapinnus piaba and Serrapinnus heterodon (Characiformes: Characidae) in a river stretch in Northeastern Brazil. Sodebras. 2013; 8(86):81–85.
  • Calhoun AJK, Mushet DM, Bell KP, Boix D, Fitzsimons JA, Isselin-Nondedeu F. Temporary wetlands: challenges and solutions to conserving a ‘disappearing’ ecosystem. Biol Conserv. 2017; 21:3–11. https://doi.org/10.1016/j.biocon.2016.11.024
    » https://doi.org/10.1016/j.biocon.2016.11.024
  • Cardoso MNM, Azevedo F, Dias A, Almeida ACS, Senna AR, Marques AC et al. Causes and effects of sampling bias on marine Western Atlantic biodiversity knowledge. Divers Distrib. 2024; 30(6):e13839. https://doi.org/10.1111/ddi.13839
    » https://doi.org/10.1111/ddi.13839
  • Castro RMC, Polaz CNM. Small-sized fish: the largest and most threatened portion of the megadiverse neotropical freshwater fish fauna. Biota Neotrop. 2019; 20(1):e20180683. https://doi.org/10.1590/1676-0611-BN-2018-0683
    » https://doi.org/10.1590/1676-0611-BN-2018-0683
  • CEARÁ. Decreto n° 28.883 de 18 de setembro de 2007. Diário Oficial do Estado: série 2, Fortaleza, CE, ano 10, n. 170, p. 1–3; 2007.
  • Centro de Referência e Informação Ambiental (CRIA). SpeciesLink network [Internet]; 2024. Available from: https://specieslink.net/
    » https://specieslink.net/
  • Chaves FDN, Sánchez-Botero JI, Garcez DS, Reis VC. Population features of Hoplosternum littorale (Hancock, 1828) (Siluriformes, Callichthyidae) at Santo Anastacio Reservoir, Brazil. Rev MVZ Cordoba. 2013; 18(3):3767–72.
  • Chiu M-C, Leigh C, Mazor R, Cid N, Resh V. Anthropogenic threats to intermittent rivers and ephemeral streams. In: Datry T, Bonada N, Boulton A, editors. Intermittent rivers and ephemeral streams. San Diego: Academic Press; 2017. p.433–54. https://doi.org/10.1016/B978-0-12-803835-2.00017-6
    » https://doi.org/10.1016/B978-0-12-803835-2.00017-6
  • Conselho Estadual do Meio Ambiente (COEMA). Resolução COEMA 54, de 24 de outubro de 2007. Homologa a lista de espécies da flora e da fauna ameaçadas no Estado do Pará. 2007. [Internet]. https://www.semas.pa.gov.br/legislacao/files/pdf/375.pdf
    » https://www.semas.pa.gov.br/legislacao/files/pdf/375.pdf
  • Companhia de Gestão dos Recursos Hídricos (COGERH). Atlas dos Recursos Hídricos do Ceará [Internet]. 2002. http://atlas.cogerh.com.br/
    » http://atlas.cogerh.com.br/
  • Conselho Estadual de Política Ambiental (COPAM). Deliberação Normativa COPAM 147, de 30 de abril de 2010. Aprova a Lista de Espécies Ameaçadas de Extinção da Fauna do Estado de Minas Gerais. 2010. [Internet]. http://www.siam.mg.gov.br/sla/download.pdf?idNorma=13192
    » http://www.siam.mg.gov.br/sla/download.pdf?idNorma=13192
  • Costa GC, Nogueira C, Machado RB, Colli GR. Sampling bias and the use of ecological niche modeling in conservation planning: a field evaluation in a biodiversity hotspot. Biodivers Conserv. 2010; 19(3):883–99. https://doi.org/10.1007/s10531-009-9746-8
    » https://doi.org/10.1007/s10531-009-9746-8
  • Costa RB, Farias JO, Sales RO. Common curimatã (Prochilodus cearaensis) in backwoodsman life in northeast Brazil. Rev Bras Hig Sanid Anim. 2016; 10(1):158–65. https://doi.org/10.5935/1981-2965.20160045
    » https://doi.org/10.5935/1981-2965.20160045
  • Departamento Nacional de Obras Contra as Secas (DNOCS). Pesca nos açudes públicos do Ceará e sua comercialização. Fortaleza: Imprensa Universitária do Ceará; 1963.
  • Estudo de Impacto Ambiental (EIA). Projeto Santa Quitéria. Volume II B. Consórcio Santa Quitéria. Tetra +. São Paulo, SP. 2021. [Internet]. Available from: https://consorciosantaquiteria.com.br/eia-rima/
    » https://consorciosantaquiteria.com.br/eia-rima/
  • Falkenberg J, Lima V, Yamada F, Ramos T, Lacerda AC. Changes in parasite communities of fishes from an intermittent river in the Brazilian semi-arid, after a major interbasin water transfer. Aquat Ecol. 2024; 58:895–916. https://doi.org/10.1007/s10452-024-10112-7
    » https://doi.org/10.1007/s10452-024-10112-7
  • Faustino ACQ, Terra BF. Ecological drivers of fish metacommunities: environmental and spatial factors surpass predation in structuring metacommunities of intermittent rivers. Ecol Freshw Fish. 2019; 29(1):145–55. https://doi.org/10.1111/eff.12502
    » https://doi.org/10.1111/eff.12502
  • Fundação do Meio Ambiente (FATMA). Resolução Consema 02, de 06 de dezembro de 2011. Lista Oficial de Espécies da Fauna Ameaçadas de Extinção no Estado de Santa Catarina. 2011. [Internet]. Available from: https://www.ima.sc.gov.br/index.php/biodiversidade/biodiversidade/fauna
    » https://www.ima.sc.gov.br/index.php/biodiversidade/biodiversidade/fauna
  • Fowler HR. Cold-blooded vertebrates from Florida, the west INDIES, Costa Rica and eastern Brazil. PNAS. 1915; 67:244–69.
  • Frederico RG, Reis VCS, Polaz CNM. Conservação de peixes de riacho: planejamento e políticas públicas. Oecol Austr. 2021; 25(2):546–64. https://doi.org/10.4257/oeco.2021.2502.20
    » https://doi.org/10.4257/oeco.2021.2502.20
  • Fricke R, Eschmeyer WN, Van der Laan R. Eschmeyer’s catalog of fishes: genera, species, references [Internet]. San Francisco: California Academy of Science; 2024. Available from: http://researcharchive.calacademy.org/research/ichthyology/catalog/fishcatmain.asp
    » http://researcharchive.calacademy.org/research/ichthyology/catalog/fishcatmain.asp
  • Gaiser T, Krol M, Frischkorn H, Araújo JC, editors. Global change and regional impacts: water availability and vulnerability of ecosystems and society in the semiarid northeast of Brazil. New York: Springer Berlin Heidelberg; 2003. https://doi.org/10.1007/978-3-642-55659-3
    » https://doi.org/10.1007/978-3-642-55659-3
  • Gonçalves-Silva M, Manna LR, Rodrigues-Filho CAS, Teixeira FK, Rezende CF. Effect of drying dynamics on the functional structure of a fish assemblage from an intermittent river network. Front Environ Sci. 2022; 10:903974. https://doi.org/10.3389/fenvs.2022.903974
    » https://doi.org/10.3389/fenvs.2022.903974
  • Gurgel JJS. Pesca e piscicultura em águas represadas do polígono das secas. Fortaleza: Ministério do Interior - Departamento Nacional de Obras Contra as Secas (MINTER-DNOCS)/Diretoria de Pesca e Piscicultura; 1979.
  • Gurgel-Lourenço RC, Rodrigues-Filho CAS, Angelini R, Garcez DS, Sánchez-Botero JI. On the relation amongst limnological factors and fish abundance in reservoirs at semiarid region. Acta Limnol Bras. 2015; 27(1):24–38. http://doi.org/10.1590/S2179-975X2414
    » http://doi.org/10.1590/S2179-975X2414
  • Gurgel-Lourenço RC, Rodrigues-Filho CAS, Bezerra LAV, Garcez DS, Sánchez-Botero JI. Length-weight relationships for freshwater fish species from humid forest enclaves at the Brazilian semiarid. J Appl Ichthyol. 2017; 33:1254–57. http://doi.org/10.1111/jai.13444
    » http://doi.org/10.1111/jai.13444
  • Gurgel-Lourenço RC, Rodrigues-Filho CAS, Pinto LM, Sánchez-Botero JI. Prolonged drought influences the taxonomic and functional structure of fish assemblages in estuaries along the Brazilian semiarid coast. Hydrobiologia. 2023; 850(20):4443–66. https://doi.org/10.1007/s10750-022-05059-5
    » https://doi.org/10.1007/s10750-022-05059-5
  • Gurgel-Lourenço RC, Sousa WA, Sánchez-Botero JI, Garcez DS. Ichthyofauna of two reservoirs in the middle Acaraú river basin, Ceará, Northeastern, Brazil. Check List. 2013; 9(6):1391–95. https://doi.org/10.15560/9.6.1391
    » https://doi.org/10.15560/9.6.1391
  • Ihering RV. Comissão técnica de piscicultura do nordeste do Brasil. Ministério da Viação e Obras Públicas. Recife: Escola de Artes Gráficas de Pernambuco; 1933.
  • Instituto Estadual de Meio Ambiente e Recursos Hídricos (IEMA). Decreto Estadual 5237, de 25 de novembro de 2022. 2022. [Internet]. Available from: https://leisestaduais.com.br/es/decreto-n-5237-2022-espirito-santo-declara-as-especies-de-fauna-ameacadas-de-extincao-no-estado-do-espirito-santo-e-da-outras-providencias
    » https://leisestaduais.com.br/es/decreto-n-5237-2022-espirito-santo-declara-as-especies-de-fauna-ameacadas-de-extincao-no-estado-do-espirito-santo-e-da-outras-providencias
  • International Union for Conservation of Nature (IUCN) Guidelines for using the IUCN Red List categories and criteria. Version 16 [Internet]. Gland; 2024. http://cmsdocs.s3.amazonaws.com/RedListGuidelines.pdf
    » http://cmsdocs.s3.amazonaws.com/RedListGuidelines.pdf
  • Kalinkat G, Jähnig SC, Jeschke JM. Exceptional body size-extinction risk relations shed new light on the freshwater biodiversity crisis. PNAS. 2017; 114(48):e10263. https://doi.org/10.1073/pnas.1717087114
    » https://doi.org/10.1073/pnas.1717087114
  • Kemp PS. Impoundments, barriers and abstractions: impact on fishes and fisheries, mitigation and future directions. In: Craig JF, editor. Freshwater fisheries ecology. Oxford: John Wiley & Sons, Ltd; 2015. p.717–69. https://doi.org/10.1002/9781118394380.ch52
    » https://doi.org/10.1002/9781118394380.ch52
  • Leal CG, Lennox GD, Ferraz SFB, Ferreira J, Gardner TA, Thomson JR et al. Integrated terrestrial-freshwater planning doubles conservation of tropical aquatic species. Science. 2021; 370(6512):117–21. https://doi.org/10.1126/science.aba7580
    » https://doi.org/10.1126/science.aba7580
  • Lima FCT. Revision of the smaller-sized dorados (Salminus), with comments on the monophyly of the genus and its biogeography (Characiformes: Bryconidae). Zootaxa. 2022; 5226(1):1–66. https://doi.org/10.11646/zootaxa.5226.1.1
    » https://doi.org/10.11646/zootaxa.5226.1.1
  • Lima SMQ, Ramos TPA, Silva MJ, Rosa RS. Diversity, distribution, and conservation of the Caatinga fishes: advances and challenges. In: Silva JMC, Leal IR, Tabarelli M, editors. Caatinga - The largest tropical dry forest region in South America. Cham: Springer; 2017. p.97–131. https://doi.org/10.1007/978-3-319-68339-3_4
    » https://doi.org/10.1007/978-3-319-68339-3_4
  • Lustosa-Costa SY, Ramos TPA, Zawadzki CH, Jacobina UP, Lima SMQ. Integrative taxonomy clarifies the armoured catfish Hypostomus pusarum (Starks) species complex (Siluriformes: Loricariidae) and reveals a new species in the drainages of Northeastern Brazil. Zool J Linn Soc Lond. 2024; 201(3):zlae059. https://doi.org/10.1093/zoolinnean/zlae059
    » https://doi.org/10.1093/zoolinnean/zlae059
  • Manna LR, Rezende CF, Mazzoni R. Effect of body size on microhabitat preferences in stream-dwelling fishes. J Appl Ichthyol. 2017; 33:193–202. https://doi.org/10.1111/jai.13320
    » https://doi.org/10.1111/jai.13320
  • Manna LR, Villéger S, Rezende CF, Mazzoni R. High intraspecific variability in morphology and diet in tropical stream fish communities. Ecol Freshw Fish. 2018; 28(1):41–52. https://doi.org/10.1111/eff.12425
    » https://doi.org/10.1111/eff.12425
  • Mapurunga MER, Pessoa YVB, Maria AH, Oliveira JS, Terra BF. A influência de filtros ambientais locais ictiofauna de riachos intermitentes. RCGS. 2024; 26(2):134–45. https://doi.org/10.35701/rcgs.v26.1027
    » https://doi.org/10.35701/rcgs.v26.1027
  • Meireles AJA, Brissac S, Schettino MP. O povo indígena Anacé e seu território tradicionalmente ocupado. Parecer Técnico N° 01/09 - Ministério Público Federal. Cadernos LEME. 2012; 4(1):115–235.
  • Menezes RS. A carpa: peixe flagelo que deve e precisa ser combatido. Ministério da Viação e Obras Públicas. Fortaleza: Departamento de Obras Contra as Secas. Serviço de Piscicultura; Publicação 171. Série I.C. 1956.
  • Menezes RS. Lista dos nomes vulgares de peixes de água doces e salobras da zona seca do nordeste e leste do Brasil. Arq Mus Nac. 1953; 42:343–88.
  • Ministério do Meio Ambiente (MMA). Portaria MMA Nº 148, de 7 de Junho de 2022. 2022. Ministério do Meio Ambiente. [Internet]. Available from: https://www.icmbio.gov.br/cepsul/images/stories/legislacao/Portaria/2020/P_mma_148_2022_altera_anexos_P_mma_443_444_445_2014_atualiza_especies_ameacadas_extincao.pdf
    » https://www.icmbio.gov.br/cepsul/images/stories/legislacao/Portaria/2020/P_mma_148_2022_altera_anexos_P_mma_443_444_445_2014_atualiza_especies_ameacadas_extincao.pdf
  • Morais JO, Pinheiro LS. The effect of semi-aridity and damming on sedimentary dynamics in estuaries - Northeastern region of Brazil. J Coastal Res. 2011; 64:1540–44.
  • Moro MF, Macêdo MB, Moura-Fé MM, Costa RC. Vegetação, unidades fitoecológicas e diversidade paisagística do estado do Ceará. Rodriguésia. 2015; 66(3):717–43. http://doi.org/10.1590/2175-7860201566305
    » http://doi.org/10.1590/2175-7860201566305
  • Olden JD, Hogan ZS, Zanden MJV. Small fish, big fish, red fish, blue fish: size-biased extinction risk of the world’s freshwater and marine fishes. Global Ecol Biogeogr. 2007; 16(6):694–701. https://doi.org/10.1111/j.1466-8238.2007.00337.x
    » https://doi.org/10.1111/j.1466-8238.2007.00337.x
  • Oliveira JS, Hughes RM, Terra BF. Fish and macroinvertebrates respond differently to seasonal drying in tropical non-perennial streams. Austral Ecol. 2024; 49(7):e13558. https://doi.org/10.1111/aec.13558
    » https://doi.org/10.1111/aec.13558
  • Oliveira JS, Santos AMP, Santos VC, Xavier ALM, Conceição ALF, Terra BF. Biodiversidade de peixes em riachos intermitentes da região semiárida brasileira (Bacia do rio Acaraú, Brasil). Essentia. 2023; 24(1):1–10.
  • Ortega JCG, Bacani I, Dorado-Rodrigues TF, Strüssmann C, Fernandes IM, Morales J et al. Effects of urbanization and environmental heterogeneity on fish assemblages in small streams. Neotrop Ichthyol. 2021; 19(3):e210050. https://doi.org/10.1590/1982-0224-2021-0050
    » https://doi.org/10.1590/1982-0224-2021-0050
  • Paraná. Livro Vermelho da Fauna Ameaçada no Estado do Paraná. Conexão Ambiental [Internet]. 2018. Available from: https://www.conexaoambiental.pr.gov.br/Pagina/Livro-Vermelho-da-Fauna-Ameacada-no-Estado-do-Parana-0
    » https://www.conexaoambiental.pr.gov.br/Pagina/Livro-Vermelho-da-Fauna-Ameacada-no-Estado-do-Parana-0
  • Parr TB, Smucker NJ, Bentsen CN, Neale MW. Potential roles of past, present, and future urbanization characteristics in producing varied stream responses. Freshw Sci. 2016; 35(1):436–43. https://doi.org/10.1086/685030
    » https://doi.org/10.1086/685030
  • Peixoto JT, Gurgel JJS. Produção e distribuição de alevinos pelas estações de piscicultura do DNOCS em 1976. Boletim Técnico do DNOCS. 1978; 36(1):5–15.
  • Pinheiro LS, Morais JO, Maia LP. The beaches of Ceará. In: Short AD, Klein AHF, editors. Brazilian beach systems. Cham: Springer; 2016. p.175–99. https://doi.org/10.1007/978-3-319-30394-9_7
    » https://doi.org/10.1007/978-3-319-30394-9_7
  • QGIS Development Team. QGIS geographic information system. Chicago, IL: Open Source Geospatial Foundation Project; 2024. https://qgis.org/pt_BR/site/
    » https://qgis.org/pt_BR/site/
  • Ramos TPA, Barros Neto LF, Ferreira KCF, Barbosa JEL. Redescription of Parotocinclus haroldoi Garavello, 1988 (Siluriformes: Loricariidae), Northeastern Brazil. Zootaxa. 2020; 4741(2):321–32. https://doi.org/10.11646/zootaxa.4751.2.7
    » https://doi.org/10.11646/zootaxa.4751.2.7
  • Ramos TPA, Ramos RTC, Ramos SAQA. Ichthyofauna of the Parnaíba river basin, Northeastern Brazil. Biota Neotrop. 2014; 14(1):e20130039. https://doi.org/10.1590/S1676-06020140039
    » https://doi.org/10.1590/S1676-06020140039
  • Ripple WJ, Wolf C, Newsome TM, Hoffmann M, Wirsing AJ, McCauley DJ. Extinction risk is most acute for the world’s largest and smallest vertebrates. PNAS. 2017; 114(40):10678–83. https://doi.org/10.1073/pnas.1702078114
    » https://doi.org/10.1073/pnas.1702078114
  • Rodrigues-Filho CAS, Gurgel-Lourenço RC, Bezerra LAV, Oliveira EF, Leitão RP, Garcez DS et al. How are local fish communities structured in Brazilian semiarid headwater streams? Hydrobiologia. 2018b; 819:93–108. https://doi.org/10.1007/s10750-018-3650-8
    » https://doi.org/10.1007/s10750-018-3650-8
  • Rodrigues-Filho CAS, Gurgel-Lourenço RC, Bezerra LAV, Sousa WA, Garcez DS, Lima SMQ et al. Ichthyofauna of the humid forest enclaves in the tablelands of Ibiapaba and Araripe, Northeastern Brazil. Biota Neotrop. 2016; 16(4):e20160273. http://doi.org/10.1590/1676-0611-BN-2016-0273
    » http://doi.org/10.1590/1676-0611-BN-2016-0273
  • Rodrigues-Filho CAS, Gurgel-Lourenço RC, Lima SMQ, Oliveira EF, Sánchez-Botero JI. What governs the functional diversity patterns of fishes in the headwater streams of the humid forest enclaves: environmental conditions, taxonomic diversity or biotic interactions? Environ Biol Fish. 2017; 100:1023–32. http://doi.org/10.1007/s10641-017-0603-4
    » http://doi.org/10.1007/s10641-017-0603-4
  • Rodrigues-Filho CAS, Gurgel-Lourenço RC, Ramos EA, Novaes JLC, Garcez DS, Costa RS et al. Metacommunity organization in an intermittent river in Brazil: the importance of riverine networks for regional biodiversity. Aquat Ecol. 2019; 54:145–61. https://doi.org/10.1007/s10452-019-09732-1
    » https://doi.org/10.1007/s10452-019-09732-1
  • Rodrigues-Filho CAS, Leitão RP, Zuanon J, Sánchez-Botero JI, Baccaro FB. Historical stability promoted higher functional specialization and originality in Neotropical stream fish assemblages. J Biogeogr. 2018a; 45(6):1345–54. http://doi.org/10.1111/jbi.13205
    » http://doi.org/10.1111/jbi.13205
  • Rosa RS, Groth F. Ictiofauna dos ecossistemas de brejos de altitude de Pernambuco e Paraíba. In: Pôrto KC, Cabral JJP, Tabarelli M, editors. Brejos de altitude em Pernambuco e Paraíba. Brasília: Ministério do Meio Ambiente; 2004. p.201–28.
  • Rosa RS, Groth F. Ictiofauna dos ecossistemas de brejos de altitude de Pernambuco e Paraíba. In: Pôrto KC, Cabral JJP, Tabarelli M, editors. Brejos de altitude em Pernambuco e Paraíba. Brasília: Ministério do Meio Ambiente; 2004. p.201–28.
  • Sabaj MH. Codes for Natural History Collections in Ichthyology and Herpetology. Copeia. 2020; 108(3):593–669. https://doi.org/10.1643/ASIHCODONS2020
    » https://doi.org/10.1643/ASIHCODONS2020
  • Sánchez-Botero JI, Garcez DS, Cascon P, Lima SMQ, Brito LBM, Roberto IJ. Anfíbios e peixes do Parque Nacional de Ubajara e Entorno - Guia Ilustrado. Fortaleza: UFC/LABOMAR/NAVE; 2014b.
  • Sánchez-Botero JI, Gurgel-Lourenço RC, Pinto LM, Leitão RP, Novaes JLC, Ramos TPA et al. Peixes estuarinos da costa semiárida do Brasil: guia ilustrado. Fortaleza: Expressão Gráfica e Editora; 2023.
  • Sánchez-Botero JI, Lourenço RCG, Rodrigues-Filho CAS, Ramos TPA, Pinto LM, Garcez DS. Lista de peixes continentais do Ceará. Fortaleza: Secretaria do Meio Ambiente do Ceará; 2021. [Internet]. Available from: https://www.sema.ce.gov.br/fauna-do-ceara/peixes
    » https://www.sema.ce.gov.br/fauna-do-ceara/peixes
  • Sánchez-Botero JI, Reis VC, Nascimento FD, Garcez DS. Fish assemblage of the Santo Anastácio reservoir (Ceará State, Brazil). Bol Inst Pesca. 2014a; 40(1):1–15.
  • Sánchez-Botero JI, Rodrigues-Filho CAS, Gurgel-Lourenço RC, Bezerra LAV, Sousa WA, Chaves FDN et al. Ecomorfologia de peixes como ferramenta na avaliação da unidade de conservação Parque Nacional de Ubajara. In: Mantovani W, Monteiro RF, Anjos L, Cariello MO, editors. Pesquisas em unidades de conservação no domínio da Caatinga: subsídios à gestão. Fortaleza: Edições UFC; 2017. p.465–79.
  • Secretaria de Meio Ambiente (SMA). Decreto 63.853, de 27 de novembro de 2018. Declara as espécies da fauna silvestre no Estado de São Paulo regionalmente extintas, as ameaçadas de extinção, as quase ameaçadas e as com dados insuficientes para avaliação. 2018. Available from: https://www.al.sp.gov.br/repositorio/legislacao/decreto/2018/decreto-63853-27.11.2018.html
    » https://www.al.sp.gov.br/repositorio/legislacao/decreto/2018/decreto-63853-27.11.2018.html
  • Secretaria do Meio Ambiente (SEMA). Decreto 51.797, de 8 de setembro de 2014. Declara as Espécies da Fauna Silvestre Ameaçadas de Extinção no Estado do Rio Grande do Sul. 2014. Available from: http://www.al.rs.gov.br/filerepository/replegis/arquivos/dec%2051.797.pdf
    » http://www.al.rs.gov.br/filerepository/replegis/arquivos/dec%2051.797.pdf
  • Secretaria do Meio Ambiente (SEMA). Fauna do Ceará. 2022. Available from: https://www.sema.ce.gov.br/faunadoceara
    » https://www.sema.ce.gov.br/faunadoceara
  • Secretaria do Meio Ambiente (SEMA). Portaria n° 37 de 15 de agosto de 2017. Lista Oficial das Espécies da Fauna Ameaçadas de Extinção do Estado da Bahia. 2017. Available from: https://dool.egba.ba.gov.br/ver-html/2765/#e:2765
    » https://dool.egba.ba.gov.br/ver-html/2765/#e:2765
  • Secretaria do Meio Ambiente (SEMA). Portaria SEMA 1, de 4 de junho de 1998. Lista Estadual da Fauna Ameaçada de Extinção do Estado do Rio de Janeiro. 1998. Available from: https://www.rcambiental.com.br/Atos/ver/PORT-SEMA-RJ-1-1998
    » https://www.rcambiental.com.br/Atos/ver/PORT-SEMA-RJ-1-1998
  • Silva AC, Sampaio SS, Viana MSR. Biologia e pesca do timbiro, Pterengraulis atherinoides, do açude Pereira de Miranda (Pentecoste, Estado do Ceará, Brasil). Acta Sci. 2005; 27(4):513–21.
  • Silva JWB, Araújo FAG. Resultados do povoamento de dez açudes públicos do Ceará, Brasil, com espécies selecionadas de peixes. Cienc Agron. 1996; 27(1/2):23–28.
  • Silva AT, Chagas RJ, Santos ACDA, Zanata AM, Rodrigues BK, Polaz CNM et al. Freshwater fishes of the Bahia State, Northeastern Brazil. Biota Neotropica. 2020a; 20(4):e20200969. https://doi.org/10.1590/1676-0611-bn-2020-0969
    » https://doi.org/10.1590/1676-0611-bn-2020-0969
  • Silva MJ, Ramos TPA, Carvalho FR, Brito MFG, Ramos RTC, Rosa RS et al. Freshwater fish richness baseline from the São Francisco Interbasin Water Transfer Project in the Brazilian Semiarid. Neotrop Ichthyol. 2020b; 18(4):e200063. https://doi.org/10.1590/1982-0224-2020-0063
    » https://doi.org/10.1590/1982-0224-2020-0063
  • Sun J, Du W, Lucas MC, Ding C, Chen J, Tao J et al. River fragmentation and barrier impacts on fishes have been greatly underestimated in the upper Mekong River. J Environ Manage. 2023; 327:116817. https://doi.org/10.1016/j.jenvman.2022.116817
    » https://doi.org/10.1016/j.jenvman.2022.116817
  • Teixeira FK, Ramos TPA, Paiva REC, Távora MA, Lima SMQ, Rezende CF. Ichthyofauna of Mundaú river basin, Ceará State, Northeastern Brazil. Biota Neotrop. 2017; 17(1):e20160174. http://doi.org/10.1590/1676-0611-BN-2016-0174
    » http://doi.org/10.1590/1676-0611-BN-2016-0174
  • Terra BF, Medeiros ESF, Sánchez-Botero JI, Novaes JLC, Rezende CF. Ecologia de peixes de riachos intermitentes. Oecol Austr. 2021; 25(2):605–19. https://doi.org/10.4257/oeco.2021.2502.23
    » https://doi.org/10.4257/oeco.2021.2502.23
  • Thomé RG, Bazzoli N, Rizzo E, Santos GB, Ratton TF. Reproductive biology of Leporinus taeniatus Lütken (Pisces, Anostomidae) in Juramento Reservoir, São Francisco River basin, Minas Gerais, Brazil. Rev Bras Zool. 2005; 22(3):565–70. https://doi.org/10.1590/S0101-81752005000300006
    » https://doi.org/10.1590/S0101-81752005000300006
  • Vorste RV, Sarrajame R, Datry T. Intermittent rivers and ephemeral streams: a unique biome with important contributions to biodiversity and ecosystem services. In: Goldstein MI, DellaSala DA, editors. Encyclopedia of the world’s biomes. Berkeley: Elsevier; 2020. p.419–29. https://doi.org/10.1016/B978-0-12-409548-9.12054-8
    » https://doi.org/10.1016/B978-0-12-409548-9.12054-8
  • Walsh CJ, Roy AH, Feminella JW, Cottingham PD, Groffman PM, Morgan RP. The urban stream syndrome: current knowledge and the search for a cure. J N Am Benthol Soc. 2005; 24(3):706–23. https://doi.org/10.1899/04-028.1
    » https://doi.org/10.1899/04-028.1
  • Zacharias I, Zamparas M. Mediterranean temporary ponds. A disappearing ecosystem. Biodivers Conserv. 2010; 19(14):3827–34. https://doi.org/10.1007/s10531-010-9933-7
    » https://doi.org/10.1007/s10531-010-9933-7

ADDITIONAL NOTES

  • Ethical Statement
    Not applicable.
  • HOW TO CITE THIS ARTICLE
    Gomes MCF, Charvet P, Pinto LM, Gurgel-Lourenço RC, Ramos TPA, Lima SMQ, Rodrigues-Filho CAS, Garcez DS, Sánchez-Botero JI.Conservation status of the freshwater fish species from Ceará State, Brazil. Neotrop Ichthyol. 2025; 23(2):e240084. https://doi.org/10.1590/1982-0224-2024-0084

Publication Dates

  • Publication in this collection
    26 May 2025
  • Date of issue
    2025

History

  • Received
    22 Aug 2024
  • Accepted
    07 Mar 2025
location_on
Sociedade Brasileira de Ictiologia Neotropical Ichthyology, Departamento de Biologia Animal e Vegetal, CCB, Universidade Estadual de Londrina, Rodovia Celso Garcia Cid, Km 380, Cidade Universitária, 86055-900, Londrina, Paraná, Brazil, Phone +55(43)3371-5151 - Londrina - PR - Brazil
E-mail: neoichth@nupelia.uem.br
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