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Continental ichthyofauna from the Paraíba do Norte River basin pre-transposition of the São Francisco River, Northeastern Brazil

Ictiofauna continental da bacia do Rio Paraíba do Norte pré-transposição do rio São Francisco, Nordeste do Brasil

Abstract:

Freshwater ichthyofauna from Brazil Northeast region was considered as being poorly known until recent years, with a considerable number of publications becoming available in the last decade. The present study provides an inventory of freshwater fish species from the Paraíba do Norte River basin located in Paraíba State, Brazil. This inventory is intended to contribute to the of knowledge to the regional fish diversity, pre-transposition of the São Francisco River. Collecting data was obtained from ichthyological databases of both national and foreign institutions. A total of 47 freshwater fish species are registered within the Paraíba do Norte River basin, represented by 38 genera, 20 families and six orders. Characiformes, comprising 47% (22 species), Cichliformes, and Siluriformes are among the most representative orders, 19% (9 species) each, of total recorded species. Seven species of Cichliformes are reported as introduced species in this basin. Cyprinodontiformes and Gobiiformes also registered in this region and correspond to 5% (two species) and Gymnotiformes, Perciformes and Synbranchiformes, 2% (one species each) of total recorded species. Paraíba do Norte River basin stands out in the current national scenario as it comprises the first region from the Mid-Northeastern Caatinga freshwater ecoregion to receive water from the transposition of the São Francisco River. The current inventory is important as it provides scientific data related to the ichthyofauna of Paraíba do Norte River basin prior to the commencement of the river transposition process. An identification key is also given for the freshwater fish species of the region.

Keywords:
Freshwater fishes; Neotropical Region; diversity; identification key

Resumo:

A ictiofauna de água doce do Nordeste brasileiro durante muito tempo foi considerada pouco conhecida. No entanto, este paradigma vem sendo mudado nas últimas décadas com aumento significativo no número de publicações desta ictiofauna. Para contribuir com mais informações sobre a diversidade de peixes do Nordeste brasileiro, o presente estudo realizou um inventário das espécies de peixes de água doce da bacia do rio Paraíba do Norte, localizada no Estado da Paraíba, pré-transposição do Rio São Francisco. Os dados foram provenientes de acervos ictiológicos de instituições nacionais e estrangeiras. Foram registradas 47 espécies, distribuídas em 38 gêneros, 20 famílias e seis ordens de peixes na bacia do rio Paraíba do Norte. As ordens mais representativas foram Characiformes (22 espécies/47% do total), Cichliformes e Siluriformes (9/19%). Sete espécies de Cichliformes são reportadas como introduzidas na bacia. Além das ordens citadas, foram registrados dois Cyprinodontiformes and Gobiiformes (2/5%), e Gymnotiformes, Perciformes e Synbranchiformes (1/2% cada). A bacia do Paraíba do Norte tem se destacado no cenário atual por ser a primeira da região Nordeste Médio-Oriental a receber águas da transposição do rio São Francisco. Com isso, este inventário é de fundamental importância, por apresentar dados da ictiofauna da bacia do rio Paraíba do Norte antes da transposição. Esse trabalho também apresenta uma chave para identificação das espécies de peixes da bacia.

Palavras-chave:
Peixes de água doce; Região Neotropical; Inventário; Chave de identificação

Introduction

Knowledge regarding freshwater fish fauna in Brazil used to be heterogeneous, with major studies focusing on the South and Southeast regions of the country with little emphasis being placed on the Northeast region (Rosa et al. 2003ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180., Langeani et al. 2009LANGEANI, F., BUCKUP, P.A., MALABARBA, L.R., PY-DANIEL, L.H.R., LUCENA, C.A.S., ROSA, R.S., ZUANON, J.A.S., LUCENA, Z.M.S., DE BRITTO, M.R., OYAKAWA, O.T. & GOMES-FILHO, G. 2009. Peixes de Água Doce. In Estado da arte e perspectivas para a zoologia no Brasil (R.M. Rocha & W.A.P. Boeger, orgs.). Ed. UFPR, Curitiba, p.211-230., Ramos et al. 2014RAMOS, T.P.A. RAMOS, R.T.C. & RAMOS, S.A.Q.A. 2014. Ichthyofauna of the Parnaíba river Basin, Northeastern Brazil. Biota Neotrop. 14(1): 1-8.). Lack of research has limited the classification of the local ichthyofaunistic diversity and delayed biogeographic evaluation of groups of fishes from Brazilian Northeastern region (Rosa et al. 2003ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180., Ramos et al. 2014RAMOS, T.P.A. RAMOS, R.T.C. & RAMOS, S.A.Q.A. 2014. Ichthyofauna of the Parnaíba river Basin, Northeastern Brazil. Biota Neotrop. 14(1): 1-8.). This paradigm has recently changed with the publication of a book chapter entitled "Diversity, patterns of distribution and conservation of fishes from Caatinga" in Rosa et al. (2003)ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180. listed 240 species of freshwater fishes for the Caatinga biome, comprising the broadest evaluation about the freshwater ichthyofauna from this region to date. Various studies have since been undertaken which the understanding of the regional ichthyofauna through publications, including: Ramos et al. (2005)RAMOS, R.T.C., RAMOS, T.P.A., ROSA, R.S., BELTRÃO, G.B.M. & GROTH, F. 2005. Diversidade de Peixes (Ictiofauna) da bacia do rio Curimataú, Paraíba. In Análise das variações da biodiversidade do bioma caatinga: suporte das estratégias regionais de conservação (F.S. Araujo, M.J.N. Rodal & M.R.V. Barbosa, eds.). Ministério do Meio Ambiente, Brasília, p. 291-318., Alves et al. (2008), Nascimento et al. (2011)NASCIMENTO, J.L. & CAMPOS, I.B. 2011. Atlas da fauna brasileira ameaçada de extinção em unidades de conservação federais. Instituto Chico Mendes de Conservação da Biodiversidade (ICMBio), Brasília., Cardoso (2012)CARDOSO, M.M.L., TORELLI, J.E.R.S., CRISPIM, M.C. & SIQUEIRA, R. 2012. Diversidade de peixes em poças de um rio intermitente do semi-árido paraibano, Brasil. Biotemas. 25(3): 161-171., Gurgel-Lourenço et al. (2013)GURGEL-LOURENÇO, R.C., SOUSA, W.A., SÁNCHEZ-BOTERO, J.I. & GARCEZ, D.S. 2013. Ichthyofauna of two reservoirs in the middle Acaraú river basin, Ceará, Northeastern Brazil. Check List. 9(6): 1391-1395., Novaes et al. (2013)NOVAES, J.L.C., MOREIRA, S.I.L., FREIRE, C.E.C., SOUSA, M.M.O. & COSTA, R.S. 2013. Fish assemblage in a semi-arid Neotropical reservoir: composition, structure and patterns of diversity and abundance. Braz. J. Biol. 74(2): 290-301., Sánchez-Botero et al. (2013)SÁNCHEZ-BOTERO, J., REIS, V.C., CHAVES, F.D.N. & GARCEZ, D. 2013. Fish assemblage of the Santo Anastácio reservoir (Ceará state, Brazil). Bol. Inst. Pesca. 40(1):1-15., Camelier & Zanata (2014)CAMELIER, P. & ZANATA, A.M. 2014. Biogeography of freshwater fishes from the Northeastern Mata Atlântica. Neotrop Ichthyol. 12(4):683-698., Nascimento et al. (2014)NASCIMENTO, J.L. & CAMPOS, I.B. 2011. Atlas da fauna brasileira ameaçada de extinção em unidades de conservação federais. Instituto Chico Mendes de Conservação da Biodiversidade (ICMBio), Brasília., Paiva et al. (2014)PAIVA, R.E.C., LIMA, S.M.Q., RAMOS, T.P.A. & MENDES, L. 2014. Fish fauna of Pratagi River coastal microbasin, extreme north Atlantic Forest, Rio Grande do Norte State, northeastern Brazil. Check List. 10(5): 968-975., Silva et al. (2014)SILVA, M.J., RAMOS, T.P.A., DINIZ, V.D., RAMOS, R.T.C. & MEDEIROS, E.S.F. 2014. Ichthyofauna of Seridó/Borborema: a semi-arid region of Brazil. Biota Neotrop. (14): 1-6., Ramos et al. (2014)RAMOS, T.P.A. RAMOS, R.T.C. & RAMOS, S.A.Q.A. 2014. Ichthyofauna of the Parnaíba river Basin, Northeastern Brazil. Biota Neotrop. 14(1): 1-8., Silva et al. (2015)SILVA, M.J., COSTA, B.G., RAMOS, T.P.A., AURICCHIO, P. & LIMA, S.M.Q. 2015. Ichthyofauna of the Gurgeia River, Parnaíba River basin, northeastern Brazil. Check List. 11: 1765., Gurgel-Lourenço et al. (2015)GURGEL-LOURENÇO, R.C., RODRIGUES-FILHO, C.A.S., ANGELINI, R., GARCEZ, D.S. & JORGE SÁNCHEZ-BOTERO, I. 2015. On the relation amongst limnological factors and fish abundance in reservoirs at semiarid region. Acta Limnol. 27(1): 24-38., Rodrigues-Filho et al. (2016)RODRIGUES-FILHO, C.A.S., GURGEL-LOURENCO, R.C., BEZERRA, L.A.V., SOUSA, W.A., GARCEZ, D.S., LIMA, S.M.Q., RAMOS, T.P.A. & BOTERO, J.I.S. 2016. Ichthyofauna of the humid forest enclaves in the tablelands of Ibiapaba and Araripe, Northeastern Brazil. Biota Neotrop. (14): e20160273., Costa et al. (2017)COSTA, S.Y.L., BARBOSA, J.E.DE L., VIANA, L.G. & RAMOS, T.P.A. 2017. Composition of the ichthyofauna in Brazilian semiarid reservoirs. Biota Neotrop. 17(3): 1-11. http://dx.doi.org/10.1590/1676-0611-bn-2017-0334.
http://dx.doi.org/10.1590/1676-0611-bn-2...
, Teixeira et al. (2017)TEIXEIRA, F.K., RAMOS, T.P.A., PAIVA, R.E.C., TÁVORA, M.A., LIMA, S.M.Q. & REZENDE, C. F. 2017. Ichthyofauna of Mundaú river basin, Ceará State, Northeastern Brazil. Biota Neotrop. 17: p. e20160174. and Oliveira-Silva et al. (2018)OLIVEIRA-SILVA, L., RAMOS, T.P.A., CARVALHO-ROCHA, Y.G.P., VIANA, K.M.P., AVELLAR, R.C., RAMOS, R.T.C. 2018. Ichthyofauna of the Mamanguape river basin, Northeastern, Brazil. Biota Neotrop. 18(3): e20170452. http://dx.doi.org/10.1590/1676-0611-BN-2017-0452
http://dx.doi.org/10.1590/1676-0611-BN-2...
.

Paraíba do Norte River basin is located entirely within the Paraíba State and it comprises one of the main basins from the Mid-Northeastern Caatinga freshwater ecoregion (MNCE - sensuRosa et al. 2003ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180., Albert et al. 2011ALBERT, J.S., PETRY, P. & REIS, R.E. 2011. Major biogeographic and phylogenetic patterns. In Historical Biogeography of Neotropical Freshwater Fishes (Albert, J.S. & Reis, R.E., eds.). Berkeley University of California Press, p.21-58.). This ecoregion bears hydrographic basins situated between São Francisco and Parnaíba River, and supplies water to Alagoas, Pernambuco, Paraíba, Rio Grande do Norte, Ceará States, as well as a small portion of Piauí State (Rosa et al. 2003ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180.). The hydrographic network Paraíba State is comprised basins of medium to short length such as those from Paraíba do Norte and Piranhas-Açu Rivers, as well as those of the Curimataú, Camaratuba, Mamanguape, Miriri, Gramame, Guaju and Abiaí Rivers, respectively (AESA 2017AESA. 2017. Plano Estadual de Recursos Hídricos do Estado da Paraíba. http/www.aesa.pb.gov.br. (last acess in: 20/02/2017).
http/www.aesa.pb.gov.br...
). Knowledge about the ichthyofauna from these river basins is limited, with most of the data available in grey literature.

Taxonomical studies related to freshwater fishes from Paraíba do Norte River basin are restricted to list of species from reservoirs such as those of Marinho et al. (2006)MARINHO, R.S.A., TORELLI J.E.R.S., SILVA, A.S. & RIBEIRO, L.L. 2006. Biodiversidade de peixes do semi-árido paraibano. Revista de Biologia e Ciências da Terra.1: 112-121, Montenegro et al. (2012)MONTENEGRO, A.K.A., TORELLI, J.E.R., CRISPIM, M.C., HERNÁNDEZ, M.I.M. & MEDEIROS, A.M.A. 2012. Ichthyofauna diversity of Taperoá II reservoir, semi-arid region of Paraíba, Brazil. Braz. J. Biol. (72)1: 113-120. and Costa et al. (2017)COSTA, S.Y.L., BARBOSA, J.E.DE L., VIANA, L.G. & RAMOS, T.P.A. 2017. Composition of the ichthyofauna in Brazilian semiarid reservoirs. Biota Neotrop. 17(3): 1-11. http://dx.doi.org/10.1590/1676-0611-bn-2017-0334.
http://dx.doi.org/10.1590/1676-0611-bn-2...
. Other studies are focused on ecological populational dynamics and communities, including those of Medeiros & Maltchik (2001)MEDEIROS, E.S.F. & MALTCHIK, L. 2001. Diversity and stability of fishes (teleostei) in a temporary river of the brazilian semiarid region. Iheringia, Sér. Zool.90., Montenegro et al. (2010)MONTENEGRO, A.K.A., TORELLI, J.E., MARINHO, R.S.A., CRISPIM, M.A., HERNANDEZ, M.I.M. 2010. Aspects of the feeding and population structure of Leporinus piau Fowler, 1941 (Actinopterygii, Characiformes, Anostomidae) of Taperoá II Dam, semiarid region of Paraíba, Brazil. Biotemas. 23: 101-110., Montenegro et al. (2011)MONTENEGRO, A. K. A., TORELLI, J. E., CRISPIM, M. C. & MEDEIROS, A. M. A. 2011. Population and feeding structure of Steindachnerina notonota Miranda-Ribeiro, 1937 (Actinopterygii, Characiformes, Curimatidae) in Taperoá II dam, semi-arid region of Paraíba, Brazil. Acta Limnol Bras. 23: 233-244., and Costa (2015)COSTA, S.Y.L. 2015. Composição taxonômica e ecologia trófica da ictiofauna em reservatórios do semiárido brasileiro. Unpublished Dissertation. Universidade Estadual da Paraíba, Campina Grande.. Studies on the taxonomy and systematics of freshwater fishes from Paraíba do Norte River basin is scarce. This is problematic and contributes to misleading future researches focusing on the biological aspects of the local species due to misidentifications.

Recently, the Paraíba do Norte River has been artificially connected to São Francisco River basin through a water transposition project (Integration Project of São Francisco River with hydrographic basins from the North Northeast - known as PISF). This project aims to eradicate hydrological shortage in the Northeast Semi-arid region (Pittock et al. 2009PITTOCK, J., MENG, J. & CHAPAGAIN, A.K. 2009. Interbasin water transfers and water scarcity in a changing world -a solution or a pipedream? A discussion paper in a burning issue, 2nd, WWF Germany, Frankfurt., Brasil 2004BRASIL. 2004. RIMA - Projeto de Integração da Bacia do Rio São Francisco com Bacias Hidrográficas do Nordeste Setentrional. Brasília: Ministério da Integração Nacional, 136p.). The transposition began in March 2017, along the east axis, which takes the waters of the São Franscisco River to the Paraíba do Norte River. Considering the difference in species composition (São Francisco, with 241 species and NMCE with 94, Barbosa et al. 2017; Oliveira-Silva et al. 2018OLIVEIRA-SILVA, L., RAMOS, T.P.A., CARVALHO-ROCHA, Y.G.P., VIANA, K.M.P., AVELLAR, R.C., RAMOS, R.T.C. 2018. Ichthyofauna of the Mamanguape river basin, Northeastern, Brazil. Biota Neotrop. 18(3): e20170452. http://dx.doi.org/10.1590/1676-0611-BN-2017-0452
http://dx.doi.org/10.1590/1676-0611-BN-2...
, respectively) and its natural history, it is expected the occurrence of biological invasions between basins, a factor already observed in researches involving the transposition of basins (e.g., Ellender & Weyl, 2014ELLENDER, B.R., WEYL, O.L.F. 2014. A review of current knowledge, risk and ecological impacts associated with non-native freshwater fish introductions in South Africa. Aquatic Invasions 9: 117-32.; Shelton et al. 2016SHELTON, J.M., CLARK, B.M., SEPHAKA, T, TURPIE, J.K. 2016. Population crash in Lesotho's endemic Maloti minnow Pseudobarbus quathlambae following invasion by translocated smallmouth yellowfish Labeobarbus aeneus. Aquatic Conservation: Marine and Freshwater Ecosystems 27: 1-13.), which could lead to the extinction of species in these ecosystems to the detriment of competition for space and resources (Pysek & Richardson, 2006PYSEK, P., RICHARDSON, D.M. 2006. The biogeography of naturalization in alien plants. Journal of Biogeography 33: 2040-2050.). The current study aimed to provide an inventory of the ichthyofauna from Paraíba do Norte River basin prior to the transposition project. Additionally, this study provides the first identification key to freshwater species from this basin.

Material and Methods

1. Study area

The hydrographical basin of Paraíba do Norte River is located between latitudes 06º51'31" and 08º26'21" South, and longitudes 34º48'35" and 37º02'15" North (Lima & Melo 1985LIMA, A.G.M. de & MELO, A.M.B.L. 1985. Atlas Geográfico do Estado da Paraíba. Relevo. In Secretária da Educação; Governo do Estado da Paraíba; Universidade Federal da Paraíba. João Pessoa (PB): Grafset. p.26-29., Xavier et al. 2013XAVIER, R.A., DORNELLAS, C.P., MACIEL, J.S. & BÚ, J.C. 2013. Caracterização do Regime fluvial da Bacia Hidrográfica do rio Paraíba - PB, Revista Tamoios, São Gonçalo (RJ). 8(2):15-28.) (Figure 1). Its area ranges a total of 20,071.83 km2 (comprising 32% of the total extension of Paraíba State), and it is considered the second largest hydrographical basin of this State.

Figure 1
Map of Paraíba do Norte River basin, Paraíba State, Brazil, showing sampling sites.

Paraíba do Norte River is the most extensive river that drains the Western of Borborema plateau in Northeastern Brazil. Its origin is located in Alto da Serra de Jabitacá (Monteiro municipality), and runs in a Southeast-Northeast direction for about 360 km until it reaches the Atlantic Ocean (Cabedelo municipality). This river crosses over one of the most drought stricken regions of the State (Cairiri Paraibano) and disembogues in the Littoral flatland. This area is characterized by a humid climate and prevalence of typical Atlantic forest vegetation (Silva 2003SILVA, L.M.T. 2003. Nas margens do Rio Paraíba do Norte. Revista Cadernos do Logepa. Série Texto Didático. Ano 2. (4).).

This river basin is divided into three portions, the higher, middle and lower portions. The main river course of the higher portion is named Meio River, and extends from its origin to Boqueirão municipality. Waters from Taperoá River, its main affluent, supply this region. The largest reservoir of this basin, Epitácio Pessoa, is currently located in the junction between these rivers. The middle portion extends from Taperoá River mouth to Paraibinha River confluency, among Itatuba and Natuba municipalities. The lower portion of this river basin begins downstream of this reservoir and extends until the river mouth which runs into the Atlantic Ocean (Lima & Melo 1985LIMA, A.G.M. de & MELO, A.M.B.L. 1985. Atlas Geográfico do Estado da Paraíba. Relevo. In Secretária da Educação; Governo do Estado da Paraíba; Universidade Federal da Paraíba. João Pessoa (PB): Grafset. p.26-29., Silva 2013, AESA 2017AESA. 2017. Plano Estadual de Recursos Hídricos do Estado da Paraíba. http/www.aesa.pb.gov.br. (last acess in: 20/02/2017).
http/www.aesa.pb.gov.br...
).

The region surrounding Paraíba do Norte River is characterized by irregular regimes of droughts and floods, semi-arid climate, and impermeable riverbeds in the high and middle portions. These characteristics induce an intermittent superficial water-flow (Silva 2013). Typical Caatinga vegetation prevails in these portions and it is characterized by the presence of deciduous shrubs and xerophytic plants (Simões et al. 2008SIMÕES, N.R., SONODA, S.L. & RIBEIRO, S.M.M.S. 2008. Spatial and seasonal variation of microcrustaceans (Cladocera and Copepoda) in intermittent rivers in the Jequiezinho River Hydrographic Basin, in the Neotropical semiarid. Acta Limnol Bras. 20(3): 197-204.). Semi-arid climate, type BS'h (warm and dry), has temperature of 26ºC and a mean annual precipitation of 600 mm, respectively (Köppen, 1936KÖPPEN, W. 1936. Das geographische System der Klimate. In Handbuch der Klimatologie (W. Köppen & R. Geiger, eds.). Gebrüder Borntraeger, Berlin, p.1−44.; Sudene 1990SUDENE. 1990. Superintendência do Desenvolvimento do Nordeste. Dados pluviométricos mensais do Nordeste. Recife: SUDENE, Série Pluviometria 1 a 10.). The lower portion of the basin is situated in the Atlantic forest vegetation with a perennial regime of superficial water-flow. The climate in this portion is humid tropical (Am) with temperatures between 24º and 27ºC and a mean annual precipitation between 900 and 1800 mm, respectively (Lima & Melo 1985LIMA, A.G.M. de & MELO, A.M.B.L. 1985. Atlas Geográfico do Estado da Paraíba. Relevo. In Secretária da Educação; Governo do Estado da Paraíba; Universidade Federal da Paraíba. João Pessoa (PB): Grafset. p.26-29.).

2. Data collection

Databases from ichthyological collections of Universidade Federal da Paraíba (UFPB) and Universidade Federal Rio Grande do Norte (UFRN) were accessed for collecting data. Other national and foreign institutions that bear a variety of representatives from the Neotropical region were also consulted, including: Museu Nacional, Rio de Janeiro (MNRJ), Museu de Zoologia da Universidade de São Paulo (MZUSP), Museu de Ciências e Tecnologia da Pontifícia Universidade Católica do Rio Grande do Sul (MCP), Universidade Federal da Bahia (UFBA), all located in Brazil; Museum of Comparative Zoology, Harvard University (MCZ) and Smithsonian National Museum of Natural History (NMNH) in the U.S.A; Museum fur Naturkunde, Berlin, Germany (ZMB); Muséum National D' Histoire Naturelle, Paris, France (MNHN); Natural History Museum (NHM), London, U.K. Digital database platforms were also accessed for obtaining data: PRONEX/Neodat (http://www.mnrj.ufrj.br), Specieslink (www.specieslink.org), GBIF (www.gibf.org), and Portal Biodiversidade/ICMBIO (https://portaldabiodiversidade.icmbio.gov.br). However, all the material included in the species list (Table 1) was analyzed and deposited in the UFPB and UFRN collections. Other institutions, whose curators claimed to have material from the studied basin, as well as data obtained from online platforms, did not register any different species when compared to the species found in the collections previously accessed (UFPB and UFRN). Therefore the data were used only to increase the distribution of the samples in the drainage. In total data from 71 sampling points were recorded (Figure 1). Some sampled areas were lacking geographic coordinates, displaying only the name of the municipalities they belonged to. In such cases, we used an approximated coordinate based on the municipality location. For that reason, we did not present any list with the geographic information of the sampling areas.

Table 1
List of Fish species of Paraíba do Norte River basin, Paraíba State, Brazil. Endemic: of MNCE; Allochthonous: introduced from other regions; Autochthonous: native to the region; Exotic: introduced from other countries. DD = deficient data, LC = Last concern, NE = not evaluated, EN = endangered, UFPB = Universidade Federal da Paraíba, UFRN = Universidade Federal do Rio Grande do Norte.

Data available in the scientific collections and online databases are results from independent initiatives of a variety of research projects. Thus, these results do not represent equivalent samplings and/or standardized collecting methodology, indicating its unfeasibility on providing comparisons about the abundance of specimens between the collection sites.

A dichotomous identification key was prepared using material held in the fish collections from UFPB and UFRN. Meristic and morphometric data were taken from Hubbs & Lagler (2004)HUBBS, C.L. & LAGLER K.F. 2004. Fishes of the Great Lakes region. University of Michigan Press.. Classification follows Eschmeyer et al. (2018)ESCHMEYER, W.N., FRICKE, R. & VAN DER LAAN, R. (eds). 2018. Catalog of fishes: genera, species, references. http://research.calacademy.org/research/ichthyology/catalog/fishcatmain.asp (the last access in 14/08/2018).
http://research.calacademy.org/research/...
. The conservation status was classified according to the Brazilian lists of endangered species, Portaria nº 445, December 17, 2014 (Brasil 2014BRASIL. 2014. Lista Nacional Oficial de Espécies da Fauna Ameaçada de Extinção - Portaria N° 443, de 17 de dezembro de 2014. Ministério do Meio Ambiente. Diário Oficial da União, Brasília, Seção 1(245): 121-130.), and 'data deficiency' (DD) species lists (ICMBio 2016ICMBio. 2016. Lista de espécies quase ameaçadas e com dados insuficientes. http://www.icmbio.gov.br/portal/faunabrasileira/lista-de-especies-dados-insuficientes (last acess in: 20/05/2018).
http://www.icmbio.gov.br/portal/faunabra...
).

Results

Material from Paraíba do Norte River basin are available in the fish collections at MCT and MCZ only. A total of 47 species of freshwater fishes are recorded and classified into 38 genera, 20 families and six orders (Table 1). There are 22 species of Characiformes that represents 47% of total recorded species, which comprises the largest order in the region (Figure 2). Species of Characiformes are spread among 17 genera and nine families. No introduced species of Characiformes were verified in this basin. The second largest order is Cichliformes and Siluriformes with 9 species each (representing 19% of total recorded species, each). Cichiformes is divided into eight genera and one family. Six introduced species of Cichliformes were registered (Astronotus ocellatus, Cichla ocellaris, Cichla monoculus, Coptodon rendalli, Parachromis managuensis and Oreochromis niloticus). The nine species of Siluriformes are distributed in seven genera and four families. Cyprinodontiformes and Gobiiformes with two species each, representing 5% of total recorded species. Within of Cyprinodontiformes, Poecilia reticulata, is considered an exotic species. Gymnotiformes, Perciformes and Synbranchiformes comprise one species each, representing 2% of total recorded species.

Figure 2
Number of species by order caught in Paraíba do Norte River basin, Paraíba State, Brazil.

Characidae (Characiformes) is the most diverse family with 10 species (or 21.3% of total recorded species) followed by Cichildae (Perciformes) and Loricariidae (Siluriformes) with nine and four species corresponding to 19.2% and 8.5% of total recorded species, respectively (Figure 3). Three species of Cichlidae are native to this region. Thus, Loricariidae comprises the second most representative group in the basin when considering only native species. Cichlidae is the third most representative group together with Erythrinidae, both with three species each (6.4% of total recorded species). Anostomidae, Callichthyidae, Curimatidae, Heptapteridae and Poeciliidae two species each, representing 4.3% of total recorded species for each family. Poeciliidae has one introduced species, Poecilia reticulata. A single species is verified for each of the other ten families (Auchenipteridae, Crenuchidae, Eleotridae, Gobiidae, Gymnotidae, Parodontidae, Prochilodontidae, Serrasalmidae, Sciaenidae, Synbranchidae and Triportheidae). Plagioscion squamosissimus is also an introduced species that belongs to the family Sciaenidae.

Figure 3
Number of species by family caught in Paraíba do Norte River basin, Paraíba State, Brazil.

Eight introduced species and 39 native species are observed out of 47 species registered in Paraíba do Norte River basin. A total of 37 native species are exclusively from freshwater environment and two species are marine-estuarine, including Awaous tajasica and Eleotris pisonis. Seven freshwater species are endemic to the MNCE (strictoRosa et al. 2003ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180.) (Table 1), in which Parotocinclus spilosoma is endemic to Paraíba do Norte River basin. Apareiodon davisi is the only threatened species among those endemic species from the MNCE. This species is currently classified as "in danger" according to the Official National List of Threatened Faunistic Species - Fishes and Aquatic Invertebrates (Brasil 2014BRASIL. 2014. Lista Nacional Oficial de Espécies da Fauna Ameaçada de Extinção - Portaria N° 443, de 17 de dezembro de 2014. Ministério do Meio Ambiente. Diário Oficial da União, Brasília, Seção 1(245): 121-130.).

Species herein evaluated are recorded from 74 sampling sites distributed throughout the three portions (higher, middle, and lower) of Paraíba do Norte River basin. A total of 5,498 specimens were counted within the 597 sampling sites. Twelve collecting sites are located within the limits of prioritization areas for conservation of the Caatinga biome (Figura 1) and 14 inside the Conservation Units.

The ichthyological collection at UFPB holds the largest number of representatives from Paraíba do Norte River basin with 4,001 specimens available and comprising 46 fish species, and distributed within 396 lots. Thus, it contains 97.9% of total ichthyofauna from the studied basin. UFRN has another important fish collection representing the diversity of the studied basin. It bears 905 specimens available, comprising 28 species (59.6% of total ichthyofauna), and distributed within 142 lots. MCZ has 219 specimens distributed within 30 lots for 30 species (63.8% of total ichthyofauna). MCT holds 366 specimens with 24 lots for 17 species (36.2% of total ichthyofauna). MZUSP only has three lots belonging to the type series of Parotocinclus jumbo (MZUSP 69513 - Holotype; MZUSP 69514 and MZUSP 69519 - Paratypes), a species described in Britski & Garavello (2002)BRITSKI, H.A. & J.C. GARAVELLO. 2002. Parotocinclus jumbo, a new species of the subfamily Hypoptopomatinae from northeastern Brazil (Ostariophysi: Loricariidae). Ichthyol. Explor. Freshwat. 13(3): 279-288.. The type locality of this species is Paraíba do Norte River, under bridge from PB-408 road, near Umbuzeiro municipality, Paraíba State, Brazil. MNRJ has a single lot from this basin (MNRJ 21924) that is regarded to be the paratype of P. jumbo, with same collecting data as the holotype of this species.

Twenty-two native species out of 39 species recorded from the studied basin occur in regions under dominion of both Caatinga and Atlantic forest biomes. Six and 11 species occur exclusively in these biomes, respectively (Table 1). Five exotic species out of eight species recorded in the area occur in both biomes. Three exotic species occur exclusively in the Caatinga biome while no exotic species are found exclusively in the Atlantic forest biome.

Discussion

Paraíba do Norte River basin has 47 fish species that correspond to 54.6% of total ichthyofauna from MNCE and 19.5% of total ichthyofauna from Caatinga biome when compared to the number of species registered in these areas (86 and 240 species, respectively, according to Rosa et al., 2003ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180.).

Siluriformes becomes the most representative group when considering only autochthone ichthyofauna. Cichliformes comprises the second most representative order in the region. This result is in agreement with Bizerril (1994)BIZERRIL, C.R.S.F. 1994. Análise taxonômica e biogeográfica da ictiofauna de água doce do leste brasileiro. Acta Biológica Leopoldensia. 16: 51-80., Mazzoni (1998)MAZZONI, R. 1998. Estrutura de comunidades e produção de peixes de um sistema fluvial costeiro de Mata Atlântica. Unpublished Ph.D. Universidade Federal de São Carlos, São Paulo., Castro (1999)CASTRO, R.M.C. 1999. Evolução da ictiofauna de riachos sul-americanos: padrões gerais e possíveis processos causais. In Ecologia de peixes de riachos: estado atual e perspectivas (E.P. Caramaschi, R. Mazzoni, C.R.S.F. Bizerril & P.R. Peres-Neto, eds.), Oecologia Brasiliensis, vol. 7, Rio de Janeiro, p. 139-155., Reis et al. (2003)REIS, R.E., KULLANDER, S.O. & FERRARIS JR., C.J. 2003. Check list of the freshwater fishes of South and Central America. Editora da Pontifícia Universidade Católica do Rio Grande do Sul. Porto Alegre, Brazil., Rosa et al. (2003)ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180., Buckup et al. (2007)BUCKUP, P.A., MENEZES, N.A. & GHAZZI, M.S. 2007. Catálogo das espécies de peixes de água doce do Brasil. Museu Nacional, Rio de Janeiro. 149 p., Serra et al. (2007)SERRA, J.P., CARVALHO, F.R. & LANGEANI, F. 2007. Ichthyofauna of the rio Itatinga in the Parque das Neblinas, Bertioga, São Paulo: composition and biogeography. Biota Neotrop. 7(1): http://dx.doi.org/10.1590/S1676-06032007000100011.
http://dx.doi.org/10.1590/S1676-06032007...
, Albert & Reis (2011)ALBERT, J.S. & REIS, R.E. 2011. Historical Biogeography of Neotropical Freshwater Fishes. University of California Press. London. England, 406p., and Ramos et al. (2014)RAMOS, T.P.A. RAMOS, R.T.C. & RAMOS, S.A.Q.A. 2014. Ichthyofauna of the Parnaíba river Basin, Northeastern Brazil. Biota Neotrop. 14(1): 1-8. that supported Characiformes and Siluriformes as the group of greatest representation in the neotropical riverine systems. Lowe-McConnel (1999)LOWE-MCCONNELL, R.H. 1999. Estudo ecológico de comunidades de peixes tropicais. São Paulo, EDUSP, 584p. reported that Siluriformes exceeds Characiformes in number of species in the South American ichthyofauna. However, the taxonomical composition varies in different basins (Bizerril 1994BIZERRIL, C.R.S.F. 1994. Análise taxonômica e biogeográfica da ictiofauna de água doce do leste brasileiro. Acta Biológica Leopoldensia. 16: 51-80.). Characiformes order stands out from those groups in the, Parnaíba, São Francisco and Paraná basins. At family level, Characidae and Loricariidae are the most representative groups in the neotropical region when considering native species (Reis et al. 2003REIS, R.E., KULLANDER, S.O. & FERRARIS JR., C.J. 2003. Check list of the freshwater fishes of South and Central America. Editora da Pontifícia Universidade Católica do Rio Grande do Sul. Porto Alegre, Brazil., Buckup et al. 2007BUCKUP, P.A., MENEZES, N.A. & GHAZZI, M.S. 2007. Catálogo das espécies de peixes de água doce do Brasil. Museu Nacional, Rio de Janeiro. 149 p.), which is in accordance to the current results for Paraíba do Norte River basin.

One collecting site from this basin is available at the list of species from MCZ. The collectors are Maj. J.M.S. Coutinho and Dr. Justa from the expedition Thayer that occurred between 1865 and 1866 in Brazil under leadership of Louis Agassiz. The collecting site is Paraíba do Norte River near João Pessoa municipality and collecting date is 2 August 1865 (Dick 1977DICK, M.M. 1977. Stations of the Thayer Expedition to Brazil 1865-1866. Breviora (444): 1-37., Higuchi 1996HIGUCHI H. 1996. An updated list of ichthyological collecting stations of the Thayer Expedition to Brazil (1865-1866). Available from: www.mcz.harvard.edu/Departments/Ichthyology/docs/Higuchi_1996_Thayer_Formated_prelim.pdf.
www.mcz.harvard.edu/Departments/Ichthyol...
). This material is very valuable because it contributes to the ichthyofauna database from this region prior to environmental impacts that have since taken place in the Northeast Brazilian region.

Environmental degradation is common in this region, directly affecting the local freshwater ichthyofauna. Anthropic changes such as dam constructions, deforestation, implementation of powerplants and distilleries, and distribution of ichthyo-toxics in the natural habitat for eradication of weed species, introduction of allochthonous species, and alterations on river courses are examples. Reduction of fish populations or extinction of local species may have occurred due to these anthropic interferences (Rosa et al. 2003ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180.). Introduction of exotic species is also very common in Northeast Brazil (Leão et al. 2011LEÃO, T.C.C., ALMEIDA, W.R. DE., DECHOUM, M.D.E.S. & ZILLER, S.R. 2011. Espécies exóticas invasoras no nordeste do Brasil: contextualização, manejo e políticas públicas. CEPAN e Instituto Hórus. 99p., Levis et al. 2013LEVIS, C., RAMOS, T.P.A. & LIMA, S.M.Q. 2013. A disputa desigual entre peixes nativos e exóticos do semiárido. ISBN: 978-85-425-0242-8. Natal: EDUFRN. 67p.) as observed in other areas of the country (Gomes et al. 2008GOMES, J.H.C., DIAS, A.C.I.M. & BRANCO, C.C. 2008. Fish assemblage composition in three reservoirs in the State of Rio de Janeiro. Acta Limnol. Bras. 20(4): 373-380., Biagioni et al. 2013BIAGIONI, R.C., RIBEIRO, A.R. & SMITH, W.S. 2013. Checklist of non-native fish species of Sorocaba River Basin, in the State of São Paulo, Brazil. Check List. 9(2): 235-239., Frota et al. 2016FROTA, A., DEPRÁ, G.C., PETENUCCI, L.M. & GRAÇA, W.J. 2016. Inventory of the fish fauna from Ivaí River basin, Paraná State, Brazil. Biota Neotrop. 16(3): 1-11. http://dx.doi.org/10.1590/1676-0611-BN-2015-0151.
http://dx.doi.org/10.1590/1676-0611-BN-2...
). Many allochthonous species were intentionally introduced in this region through national campaigns from the Departamento Nacional de Obras Contra a Seca (DNOCS) in the 1930 decade, especially in the MNCE basin. Tucunaré (Cichla ocellaris and C. temensis) and pescada-do-Piauí (Plagioscion squamosissimus), originally from Amazonas and Parnaíba basins respectively, are examples of introduced species through DNOCS campaigns. African tilapias (Oreochromis niloticus and Coptodon rendalli) (Gurgel & Fernando 1994GURGEL, J.J.S. & FERNANDO, C.H. 1994. Fishes in semi-arid northeast Brazil with special reference to the role of tilapias. Internationale Revue der gesamten Hydrobiologie und Hydrographie. 79(1): 77-94., Reaser et al. 2005REASER, J.K., GALINDO-LEAL, C. & ZILLER, S.R. 2005. Visitas indesejadas: a invasão de espécies exóticas. In Mata Atlântica Biodiversidade, Ameaças e Perspectivas (C. Galindo-Leal e I.G. Câmara eds.). Fundação SOS Mata Atlântica e Conservação Internacional, Belo Horizonte. p. 392-405., Paiva & Mesquita 2013PAIVA, M.P. & MESQUITA, P.E.C. 2013. Uma semente fecunda: Comissão Técnica de Piscicultura do Nordeste (1932 - 1945). Revista do Instituto do Ceará. p.10-40.) are also examples of species introduced through DNOCS. Parachromis managuensis is registered for the first time in Paraíba do Norte River basin at Soledade dam. This Cichlidae species is originally from the east side of Central America (Conkel 1993CONKEL, D. 1993. Cichlids of North and Central America. Tropical Fish Hobbyist Publications, Inc., Neptune City, New York, 118p.), and has been introduced in many countries, including Brazil (Agasen et al. 2006AGASEN, E.V., CLEMENTE, J.P., ROSANA, M.R. & KAWIT, N.S. 2006. Biological investigation of Jaguar Guapote Parachromis managuensis (Gunther) in Taal Lake, Philippines. Journal of Environmental Science and Management. 9(2): 20-30., Barros et al. 2012BARROS, L.C., SANTOS, U., ZANUNCIO, J.C. & DERGAM, J.A. 2012. Plagioscion squamosissimus (Sciaenidae) and Parachromis managuensis (Cichlidae): A threat to native fishes of the Doce river in Minas Gerais, Brazil. Plos One. 7: 39138. http://dx.doi.org/10.1371/journal.pone.0039138.
http://dx.doi.org/10.1371/journal.pone.0...
). Barbosa et al. (2006)BARBOSA, J.M., MENDONÇA, I.T.L. & PONZI JR., M. 2006. Comportamento Social e Crescimento em Parachromis managuensis (Günther, 1867) (Pisces, Cichlidae): Uma Espécie Introduzida no Brasil. Revista Brasileira de Engenharia de Pesca. 1(1): 65-74. first recorded P. managuensis in Northeast Brazil at the middle portion of São Francisco River. It piscivorous and aggressive species that reaches up to 65 cm total length (Conkel 1993CONKEL, D. 1993. Cichlids of North and Central America. Tropical Fish Hobbyist Publications, Inc., Neptune City, New York, 118p., Barbosa et al. 2006BARBOSA, J.M., MENDONÇA, I.T.L. & PONZI JR., M. 2006. Comportamento Social e Crescimento em Parachromis managuensis (Günther, 1867) (Pisces, Cichlidae): Uma Espécie Introduzida no Brasil. Revista Brasileira de Engenharia de Pesca. 1(1): 65-74., Barros et al. 2012BARROS, L.C., SANTOS, U., ZANUNCIO, J.C. & DERGAM, J.A. 2012. Plagioscion squamosissimus (Sciaenidae) and Parachromis managuensis (Cichlidae): A threat to native fishes of the Doce river in Minas Gerais, Brazil. Plos One. 7: 39138. http://dx.doi.org/10.1371/journal.pone.0039138.
http://dx.doi.org/10.1371/journal.pone.0...
).

Metynnis lippincottianus, known locally as "peixe CD", is reported to occur at the lower portion of Paraíba do Norte River basin according to the fishing community. This species was previously recorded in other regional basins such as Gramame in Paraíba State (Beltrão et al. 2009BELTRÃO, G.B.M., MEDEIROS, E.S.F. & RAMOS, R.T.C. 2009. Effects of riparian vegetation on the structure of the marginal aquatic habitat and the associated fish assemblage in a tropical Brazilian reservoir. Biota Neotrop. 9(4): 37-43. http://dx.doi.org/10.1590/S1676-06032009000400003.
http://dx.doi.org/10.1590/S1676-06032009...
), Pratagi (Paiva et al. 2014PAIVA, R.E.C., LIMA, S.M.Q., RAMOS, T.P.A. & MENDES, L. 2014. Fish fauna of Pratagi River coastal microbasin, extreme north Atlantic Forest, Rio Grande do Norte State, northeastern Brazil. Check List. 10(5): 968-975.), Maxaranguape, Ceará-Mirim and Pirangí River basins (Nascimento et al. 2014NASCIMENTO, W.S., BARROS, N.H.C., ARAÚJO, A.S., GURGEL, L.L., CANAN, B., MOLINA, W.F., ROSA, R.S. & CHELLAPPA, S. 2014. Composição da ictiofauna das bacias hidrográficas do Rio Grande do Norte, Brasil. Biota Amazônia 4(1): 126-131. http://dx.doi.org/10.18561/2179 5746/biotaamazonia.v4n1p126-131
http://dx.doi.org/10.18561/2179 5746/bio...
), all located in Rio Grande do Norte State. Beltrão et al. (2009)BELTRÃO, G.B.M., MEDEIROS, E.S.F. & RAMOS, R.T.C. 2009. Effects of riparian vegetation on the structure of the marginal aquatic habitat and the associated fish assemblage in a tropical Brazilian reservoir. Biota Neotrop. 9(4): 37-43. http://dx.doi.org/10.1590/S1676-06032009000400003.
http://dx.doi.org/10.1590/S1676-06032009...
considers M. lippincottianus as an introduced species in Gramame River basin. However, other authors recognize it as a native species from Northeast river basins Canan & Gurgel (1997)CANAN, B. & GURGEL, H.D.C.B. 1997. Estrutura populacional de Metynnis roosevelti Eigenmann, 1915 (Characidae, Myleinae) da lagoa do Jiqui, Parnamirim, Rio Grande do Norte. Rev. UNIMAR. 19(2): 479-491., Rosa et al. (2003)ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180., Morais et al. (2012)MORAIS, A.L.S., PESSOA, E.K.R., CHELLAPPA, S. & CHELLAPPA, N.T. 2012. Composição ictiofaunística da Lagoa do Jiqui, Rio Grande do Norte, Brasil. Biota Amazônia. 2(1): 51-58., Nascimento et al. (2014)NASCIMENTO, W.S., BARROS, N.H.C., ARAÚJO, A.S., GURGEL, L.L., CANAN, B., MOLINA, W.F., ROSA, R.S. & CHELLAPPA, S. 2014. Composição da ictiofauna das bacias hidrográficas do Rio Grande do Norte, Brasil. Biota Amazônia 4(1): 126-131. http://dx.doi.org/10.18561/2179 5746/biotaamazonia.v4n1p126-131
http://dx.doi.org/10.18561/2179 5746/bio...
, and Paiva et al. (2014)PAIVA, R.E.C., LIMA, S.M.Q., RAMOS, T.P.A. & MENDES, L. 2014. Fish fauna of Pratagi River coastal microbasin, extreme north Atlantic Forest, Rio Grande do Norte State, northeastern Brazil. Check List. 10(5): 968-975.. Metynnis roosevelti Eigenmann, 1915 is usually cited in many studies although this species has been considered a junior synonym of M. lippincottianus (Cope 1870) in Zarske & Géry (1999)ZA ZARSKE, A. & GÉRY, J. 1999. Revision der neotropischen Gattung Metynnis Cope, 1878. 1. Evaluation der Typusexemplare der nominellen Arten (Teleostei: Characiformes: Serrasalmidae). Zoologische Abhandlungen (Dresden). 50(2): 169-216. The oldest record of Metynnis in the MNCE region is provided in Starks (1913)STARKS, E.C. 1913. The fishes of the Stanford Expedition to Brazil. Palo Alto: Stanford University Publications. as M. maculatus (Kner 1858), collected in Papary lake, Trairi River basin, Rio Grande do Norte State. The species was collected 20 years prior to the introduction of fish species in the region as described earlier in this study. There is no species from this genus listed as introduced species from the Northeast region (Leão et al. 2011LEÃO, T.C.C., ALMEIDA, W.R. DE., DECHOUM, M.D.E.S. & ZILLER, S.R. 2011. Espécies exóticas invasoras no nordeste do Brasil: contextualização, manejo e políticas públicas. CEPAN e Instituto Hórus. 99p., Levis et al. 2013LEVIS, C., RAMOS, T.P.A. & LIMA, S.M.Q. 2013. A disputa desigual entre peixes nativos e exóticos do semiárido. ISBN: 978-85-425-0242-8. Natal: EDUFRN. 67p., Gurgel & Oliveira, 1987GURGEL, J.J.S. & OLIVEIRA, A.G. 1987. Efeitos da introdução de peixes e crustáceos no semi-árido do Nordeste brasileiro. Coleção Mossoroense. 455(1): 7-32.). Thus, M. lippincottianus is supported herein as a non-introduced species in the MNCE region.

Two marine-estuarine species were observed at the studied basin, Awaous tajasica and Eleotris pisonis. These species have broad distributions along the Brazilian coast, and occasionally occur in the freshwater environment (Kullander 2003KULLANDER, S.O. 2003. Family Cichlidae. In Check list of the freshwater fishes of South and Central America (R.E. Reis, S.O. Kullander & C.J. Ferraris Jr., eds.). Edipucrs, Porto Alegre, p.605-654.). It is important to notice that the first species also occurs in the Caatinga biome, which is an area outside the Atlantic forest region. Another important record is the presence of the, Cheirodon jaguaribensis, described from Jaguaribe River, Ceará State in Fowler (1941)FOWLER, H.W. 1941. A collection of freshwater fishes Basin, Brazil, with notes on phylogeny and biogeography of annual fishes obtained in Eastern Brazil by Dr. Rodolph Von Ihering. Proceedings of the Academy of Natural Sciences of Philadelphia 93: 123-193. and considered restricted to this basin (Reis et al. 2003REIS, R.E., KULLANDER, S.O. & FERRARIS JR., C.J. 2003. Check list of the freshwater fishes of South and Central America. Editora da Pontifícia Universidade Católica do Rio Grande do Sul. Porto Alegre, Brazil., Buckup et al. 2007BUCKUP, P.A., MENEZES, N.A. & GHAZZI, M.S. 2007. Catálogo das espécies de peixes de água doce do Brasil. Museu Nacional, Rio de Janeiro. 149 p.). However, the current results also recognize this species to occur in Paraíba do Norte River basin. Occurrences of this species in other basins within the MNCE ecoregion in Texeira et al. (2017) and Gouveia et al. (2017)GOUVEIA, R.S.D., LIRA, G.L.A., RAMOS, T.P.A., MEDEIROS, E.S.F. 2017. Ichthyofauna of the Reserva Biológica Guaribas and surrounding areas, state of Paraíba, Brazil. Check List. 13(5): 581-590. https://doi.org/10.15560/13.5.581.
https://doi.org/10.15560/13.5.581...
indicate that C. jaguaribensis is not restricted to the Jaguaribe River.

There are seven official Conservation Units (UCs) in Paraíba do Norte hydrographic network: Parque Estadual do Poeta e Repentista Juvenal de Oliveira (419,51 ha), Parque Estadual Mata do Xém-Xém (182,00 ha), Área de Proteção Ambiental (APA) do Cariri (18.560,00 ha), Área de Proteção Ambiental (APA) das Onças (36.000,00 ha) all under State supervision; and three private reserves, including Reservas Particular do Patrimônio Natural (RPPN), RPPN Fazenda Almas (3.505,00 ha), RPPN Fazenda Santa Clara (750,50 ha) and RPPN Fazenda Pacatuba (266,53 ha) with a total of 59.685,54 ha of protected land. There are fish records in RPPN Fazenda Almas and Fazenda Pacatuba, and at the Parque Estadual Mata do Xém-Xém. Twenty-seven species were recorded from the UCs, comprising 71% of the native ichthyofauna of Paraíba do Norte River basin.

The source of the Paraíba do Norte River is located at Serra de Jabitacá, a region known to also separate water to the Pajeú River sub-basin which is an affluent from the São Francisco River. Paraíba do Norte River basin shares 20 native species with São Francisco River basin out of 38 native species recognized in the present study. Ten species originally from this basin were introduced at MNCE basins: Brycon hilarii (Valenciennes, 1850), Conorhynchos conirostris (Valenciennes, 1840), Franciscodoras marmoratus (Lütken, 1874), Megaleporinus elongatus (Valenciennes, 1850), Myleus micans (Lütken 1875), Pachyurus francisci (Cuvier, 1830), Pachyurus squamipennis Agassiz, 1831 and Pimelodus maculatus Lacepède, 1803 (Gurgel & Oliveira 1987GURGEL, J.J.S. & OLIVEIRA, A.G. 1987. Efeitos da introdução de peixes e crustáceos no semi-árido do Nordeste brasileiro. Coleção Mossoroense. 455(1): 7-32.). Neither of these species was recorded in the Paraíba do Norte river basin in this work.

Water transposition between different river basins has contributed to impacts in the diversity and abundance of local fish fauna (Izique 2005IZIQUE, C. 2005. As águas vão rolar; transposição do rio São Francisco divide opiniões e instiga polêmica entre governo e pesquisadores. Pesquisa FAPESP, 112: 26-29.). Transposition of waters from São Francisco River to MNCE basins aimed to supply water for local populations that suffer from regular drought crises due to intermittent river flows. Paraíba do Norte (Paraíba), Apodi-Mossoró (Rio Grande do Norte), Jaguaribe (Ceará) and Piranhas-Açu (Paraíba, Rio Grande do Norte) river basins were connected artificially to water channels from São Francisco River (Pittock et al. 2009PITTOCK, J., MENG, J. & CHAPAGAIN, A.K. 2009. Interbasin water transfers and water scarcity in a changing world -a solution or a pipedream? A discussion paper in a burning issue, 2nd, WWF Germany, Frankfurt.). The first basin to receive waters from this process was Paraíba do Norte River basin, and thus it has its regime changed to perennial. According to Moreira-Filho & Buckup (2005)MOREIRA-FILHO, O. & BUCKUP, P.A. 2005. A poorly known case of watershed transposition between the São Francisco and upper Paraná river basins. Scientific note. Neotrop Ichthyol. 3(3): 449-452., changes in species composition and abundance are imminent after water transposition took place. Consequences include competition among species, propagation of populations over others, and possibly extinction of native species.

The current inventory of freshwater fish species from Paraíba do Norte River basin is of importance as it provides an updated list of the local ichthyofauna, and contributes to the improvement of the knowledge about the diversity and evolutionary history of freshwater fish species from the region. The current study also provides an ichthyological overview of its composition prior to systemic anthropic interferences in the environment through the water transposition from São Francisco River, which will contribute to future comparative studies for understanding the environmental changes in the region.

Acknowledgments

The authors thank curators and staff from Museu Nacional do Rio de Janeiro (MNRJ), Museu de Zoologia da Universidade de São Paulo (MZUSP), Museu de Ciências e Tecnologia da Pontifícia Universidade Católica do Rio Grande do Sul (MCT), Universidade Federal da Bahia (UFBA), Museum of Comparative Zoology, Harvard University (MCZ), Smithsonian National Museum of Natural History (NMNH), Museum fur Naturkunde (ZMB), Muséum National D' Histoire Naturelle and Natural History Museum, London (MNHM) for providing relevant information related to specimens included in this study. Special thanks to Dr. Ricardo Rosa (UFPB) and Dr. Sergio Lima (UFRN) for assisting with specimen data, and Dr. Robson Tamar (UFPB) for his contributions on the development of this study.

Supplementary material

The following online material is available for this article:

Appendix: Identification key to fish species from Paraíba of North River basin

References

  • AESA. 2017. Plano Estadual de Recursos Hídricos do Estado da Paraíba. http/www.aesa.pb.gov.br (last acess in: 20/02/2017).
    » http/www.aesa.pb.gov.br
  • AGASEN, E.V., CLEMENTE, J.P., ROSANA, M.R. & KAWIT, N.S. 2006. Biological investigation of Jaguar Guapote Parachromis managuensis (Gunther) in Taal Lake, Philippines. Journal of Environmental Science and Management. 9(2): 20-30.
  • ALBERT, J.S. & REIS, R.E. 2011. Historical Biogeography of Neotropical Freshwater Fishes. University of California Press. London. England, 406p.
  • ALBERT, J.S., PETRY, P. & REIS, R.E. 2011. Major biogeographic and phylogenetic patterns. In Historical Biogeography of Neotropical Freshwater Fishes (Albert, J.S. & Reis, R.E., eds.). Berkeley University of California Press, p.21-58.
  • BARBOSA, J.M., MENDONÇA, I.T.L. & PONZI JR., M. 2006. Comportamento Social e Crescimento em Parachromis managuensis (Günther, 1867) (Pisces, Cichlidae): Uma Espécie Introduzida no Brasil. Revista Brasileira de Engenharia de Pesca. 1(1): 65-74.
  • BARROS, L.C., SANTOS, U., ZANUNCIO, J.C. & DERGAM, J.A. 2012. Plagioscion squamosissimus (Sciaenidae) and Parachromis managuensis (Cichlidae): A threat to native fishes of the Doce river in Minas Gerais, Brazil. Plos One. 7: 39138. http://dx.doi.org/10.1371/journal.pone.0039138
    » http://dx.doi.org/10.1371/journal.pone.0039138
  • BELTRÃO, G.B.M., MEDEIROS, E.S.F. & RAMOS, R.T.C. 2009. Effects of riparian vegetation on the structure of the marginal aquatic habitat and the associated fish assemblage in a tropical Brazilian reservoir. Biota Neotrop. 9(4): 37-43. http://dx.doi.org/10.1590/S1676-06032009000400003
    » http://dx.doi.org/10.1590/S1676-06032009000400003
  • BIAGIONI, R.C., RIBEIRO, A.R. & SMITH, W.S. 2013. Checklist of non-native fish species of Sorocaba River Basin, in the State of São Paulo, Brazil. Check List. 9(2): 235-239.
  • BIZERRIL, C.R.S.F. 1994. Análise taxonômica e biogeográfica da ictiofauna de água doce do leste brasileiro. Acta Biológica Leopoldensia. 16: 51-80.
  • BRASIL. 2004. RIMA - Projeto de Integração da Bacia do Rio São Francisco com Bacias Hidrográficas do Nordeste Setentrional Brasília: Ministério da Integração Nacional, 136p.
  • BRASIL. 2014. Lista Nacional Oficial de Espécies da Fauna Ameaçada de Extinção - Portaria N° 443, de 17 de dezembro de 2014. Ministério do Meio Ambiente. Diário Oficial da União, Brasília, Seção 1(245): 121-130.
  • BRITSKI, H.A. & J.C. GARAVELLO. 2002. Parotocinclus jumbo, a new species of the subfamily Hypoptopomatinae from northeastern Brazil (Ostariophysi: Loricariidae). Ichthyol. Explor. Freshwat. 13(3): 279-288.
  • BUCKUP, P.A., MENEZES, N.A. & GHAZZI, M.S. 2007. Catálogo das espécies de peixes de água doce do Brasil. Museu Nacional, Rio de Janeiro. 149 p.
  • CAMELIER, P. & ZANATA, A.M. 2014. Biogeography of freshwater fishes from the Northeastern Mata Atlântica. Neotrop Ichthyol. 12(4):683-698.
  • CANAN, B. & GURGEL, H.D.C.B. 1997. Estrutura populacional de Metynnis roosevelti Eigenmann, 1915 (Characidae, Myleinae) da lagoa do Jiqui, Parnamirim, Rio Grande do Norte. Rev. UNIMAR. 19(2): 479-491.
  • CARDOSO, M.M.L., TORELLI, J.E.R.S., CRISPIM, M.C. & SIQUEIRA, R. 2012. Diversidade de peixes em poças de um rio intermitente do semi-árido paraibano, Brasil. Biotemas. 25(3): 161-171.
  • CASTRO, R.M.C. 1999. Evolução da ictiofauna de riachos sul-americanos: padrões gerais e possíveis processos causais. In Ecologia de peixes de riachos: estado atual e perspectivas (E.P. Caramaschi, R. Mazzoni, C.R.S.F. Bizerril & P.R. Peres-Neto, eds.), Oecologia Brasiliensis, vol. 7, Rio de Janeiro, p. 139-155.
  • CONKEL, D. 1993. Cichlids of North and Central America. Tropical Fish Hobbyist Publications, Inc., Neptune City, New York, 118p.
  • COSTA, S.Y.L. 2015. Composição taxonômica e ecologia trófica da ictiofauna em reservatórios do semiárido brasileiro. Unpublished Dissertation. Universidade Estadual da Paraíba, Campina Grande.
  • COSTA, S.Y.L., BARBOSA, J.E.DE L., VIANA, L.G. & RAMOS, T.P.A. 2017. Composition of the ichthyofauna in Brazilian semiarid reservoirs. Biota Neotrop. 17(3): 1-11. http://dx.doi.org/10.1590/1676-0611-bn-2017-0334
    » http://dx.doi.org/10.1590/1676-0611-bn-2017-0334
  • DICK, M.M. 1977. Stations of the Thayer Expedition to Brazil 1865-1866. Breviora (444): 1-37.
  • ELLENDER, B.R., WEYL, O.L.F. 2014. A review of current knowledge, risk and ecological impacts associated with non-native freshwater fish introductions in South Africa. Aquatic Invasions 9: 117-32.
  • ESCHMEYER, W.N., FRICKE, R. & VAN DER LAAN, R. (eds). 2018. Catalog of fishes: genera, species, references. http://research.calacademy.org/research/ichthyology/catalog/fishcatmain.asp (the last access in 14/08/2018).
    » http://research.calacademy.org/research/ichthyology/catalog/fishcatmain.asp
  • FOWLER, H.W. 1941. A collection of freshwater fishes Basin, Brazil, with notes on phylogeny and biogeography of annual fishes obtained in Eastern Brazil by Dr. Rodolph Von Ihering. Proceedings of the Academy of Natural Sciences of Philadelphia 93: 123-193.
  • FROTA, A., DEPRÁ, G.C., PETENUCCI, L.M. & GRAÇA, W.J. 2016. Inventory of the fish fauna from Ivaí River basin, Paraná State, Brazil. Biota Neotrop. 16(3): 1-11. http://dx.doi.org/10.1590/1676-0611-BN-2015-0151
    » http://dx.doi.org/10.1590/1676-0611-BN-2015-0151
  • GOMES, J.H.C., DIAS, A.C.I.M. & BRANCO, C.C. 2008. Fish assemblage composition in three reservoirs in the State of Rio de Janeiro. Acta Limnol. Bras. 20(4): 373-380.
  • GOUVEIA, R.S.D., LIRA, G.L.A., RAMOS, T.P.A., MEDEIROS, E.S.F. 2017. Ichthyofauna of the Reserva Biológica Guaribas and surrounding areas, state of Paraíba, Brazil. Check List. 13(5): 581-590. https://doi.org/10.15560/13.5.581
    » https://doi.org/10.15560/13.5.581
  • GURGEL, J.J.S. & OLIVEIRA, A.G. 1987. Efeitos da introdução de peixes e crustáceos no semi-árido do Nordeste brasileiro. Coleção Mossoroense. 455(1): 7-32.
  • GURGEL, J.J.S. & FERNANDO, C.H. 1994. Fishes in semi-arid northeast Brazil with special reference to the role of tilapias. Internationale Revue der gesamten Hydrobiologie und Hydrographie. 79(1): 77-94.
  • GURGEL-LOURENÇO, R.C., SOUSA, W.A., SÁNCHEZ-BOTERO, J.I. & GARCEZ, D.S. 2013. Ichthyofauna of two reservoirs in the middle Acaraú river basin, Ceará, Northeastern Brazil. Check List. 9(6): 1391-1395.
  • GURGEL-LOURENÇO, R.C., RODRIGUES-FILHO, C.A.S., ANGELINI, R., GARCEZ, D.S. & JORGE SÁNCHEZ-BOTERO, I. 2015. On the relation amongst limnological factors and fish abundance in reservoirs at semiarid region. Acta Limnol. 27(1): 24-38.
  • HIGUCHI H. 1996. An updated list of ichthyological collecting stations of the Thayer Expedition to Brazil (1865-1866). Available from: www.mcz.harvard.edu/Departments/Ichthyology/docs/Higuchi_1996_Thayer_Formated_prelim.pdf
    » www.mcz.harvard.edu/Departments/Ichthyology/docs/Higuchi_1996_Thayer_Formated_prelim.pdf
  • HUBBS, C.L. & LAGLER K.F. 2004. Fishes of the Great Lakes region. University of Michigan Press.
  • IZIQUE, C. 2005. As águas vão rolar; transposição do rio São Francisco divide opiniões e instiga polêmica entre governo e pesquisadores. Pesquisa FAPESP, 112: 26-29.
  • ICMBio. 2016. Lista de espécies quase ameaçadas e com dados insuficientes. http://www.icmbio.gov.br/portal/faunabrasileira/lista-de-especies-dados-insuficientes (last acess in: 20/05/2018).
    » http://www.icmbio.gov.br/portal/faunabrasileira/lista-de-especies-dados-insuficientes
  • KÖPPEN, W. 1936. Das geographische System der Klimate. In Handbuch der Klimatologie (W. Köppen & R. Geiger, eds.). Gebrüder Borntraeger, Berlin, p.1−44.
  • KULLANDER, S.O. 2003. Family Cichlidae. In Check list of the freshwater fishes of South and Central America (R.E. Reis, S.O. Kullander & C.J. Ferraris Jr., eds.). Edipucrs, Porto Alegre, p.605-654.
  • LANGEANI, F., BUCKUP, P.A., MALABARBA, L.R., PY-DANIEL, L.H.R., LUCENA, C.A.S., ROSA, R.S., ZUANON, J.A.S., LUCENA, Z.M.S., DE BRITTO, M.R., OYAKAWA, O.T. & GOMES-FILHO, G. 2009. Peixes de Água Doce. In Estado da arte e perspectivas para a zoologia no Brasil (R.M. Rocha & W.A.P. Boeger, orgs.). Ed. UFPR, Curitiba, p.211-230.
  • LEÃO, T.C.C., ALMEIDA, W.R. DE., DECHOUM, M.D.E.S. & ZILLER, S.R. 2011. Espécies exóticas invasoras no nordeste do Brasil: contextualização, manejo e políticas públicas. CEPAN e Instituto Hórus. 99p.
  • LEVIS, C., RAMOS, T.P.A. & LIMA, S.M.Q. 2013. A disputa desigual entre peixes nativos e exóticos do semiárido. ISBN: 978-85-425-0242-8. Natal: EDUFRN. 67p.
  • LIMA, A.G.M. de & MELO, A.M.B.L. 1985. Atlas Geográfico do Estado da Paraíba. Relevo. In Secretária da Educação; Governo do Estado da Paraíba; Universidade Federal da Paraíba. João Pessoa (PB): Grafset. p.26-29.
  • LOWE-MCCONNELL, R.H. 1999. Estudo ecológico de comunidades de peixes tropicais. São Paulo, EDUSP, 584p.
  • MARINHO, R.S.A., TORELLI J.E.R.S., SILVA, A.S. & RIBEIRO, L.L. 2006. Biodiversidade de peixes do semi-árido paraibano. Revista de Biologia e Ciências da Terra.1: 112-121
  • MAZZONI, R. 1998. Estrutura de comunidades e produção de peixes de um sistema fluvial costeiro de Mata Atlântica. Unpublished Ph.D. Universidade Federal de São Carlos, São Paulo.
  • MEDEIROS, E.S.F. & MALTCHIK, L. 2001. Diversity and stability of fishes (teleostei) in a temporary river of the brazilian semiarid region. Iheringia, Sér. Zool.90.
  • MONTENEGRO, A.K.A., TORELLI, J.E.R., CRISPIM, M.C., HERNÁNDEZ, M.I.M. & MEDEIROS, A.M.A. 2012. Ichthyofauna diversity of Taperoá II reservoir, semi-arid region of Paraíba, Brazil. Braz. J. Biol. (72)1: 113-120.
  • MONTENEGRO, A. K. A., TORELLI, J. E., CRISPIM, M. C. & MEDEIROS, A. M. A. 2011. Population and feeding structure of Steindachnerina notonota Miranda-Ribeiro, 1937 (Actinopterygii, Characiformes, Curimatidae) in Taperoá II dam, semi-arid region of Paraíba, Brazil. Acta Limnol Bras. 23: 233-244.
  • MONTENEGRO, A.K.A., TORELLI, J.E., MARINHO, R.S.A., CRISPIM, M.A., HERNANDEZ, M.I.M. 2010. Aspects of the feeding and population structure of Leporinus piau Fowler, 1941 (Actinopterygii, Characiformes, Anostomidae) of Taperoá II Dam, semiarid region of Paraíba, Brazil. Biotemas. 23: 101-110.
  • MORAIS, A.L.S., PESSOA, E.K.R., CHELLAPPA, S. & CHELLAPPA, N.T. 2012. Composição ictiofaunística da Lagoa do Jiqui, Rio Grande do Norte, Brasil. Biota Amazônia. 2(1): 51-58.
  • MOREIRA-FILHO, O. & BUCKUP, P.A. 2005. A poorly known case of watershed transposition between the São Francisco and upper Paraná river basins. Scientific note. Neotrop Ichthyol. 3(3): 449-452.
  • NASCIMENTO, J.L. & CAMPOS, I.B. 2011. Atlas da fauna brasileira ameaçada de extinção em unidades de conservação federais. Instituto Chico Mendes de Conservação da Biodiversidade (ICMBio), Brasília.
  • NASCIMENTO, W.S., BARROS, N.H.C., ARAÚJO, A.S., GURGEL, L.L., CANAN, B., MOLINA, W.F., ROSA, R.S. & CHELLAPPA, S. 2014. Composição da ictiofauna das bacias hidrográficas do Rio Grande do Norte, Brasil. Biota Amazônia 4(1): 126-131. http://dx.doi.org/10.18561/2179 5746/biotaamazonia.v4n1p126-131
    » http://dx.doi.org/10.18561/2179 5746/biotaamazonia.v4n1p126-131
  • NOVAES, J.L.C., MOREIRA, S.I.L., FREIRE, C.E.C., SOUSA, M.M.O. & COSTA, R.S. 2013. Fish assemblage in a semi-arid Neotropical reservoir: composition, structure and patterns of diversity and abundance. Braz. J. Biol. 74(2): 290-301.
  • OLIVEIRA-SILVA, L., RAMOS, T.P.A., CARVALHO-ROCHA, Y.G.P., VIANA, K.M.P., AVELLAR, R.C., RAMOS, R.T.C. 2018. Ichthyofauna of the Mamanguape river basin, Northeastern, Brazil. Biota Neotrop. 18(3): e20170452. http://dx.doi.org/10.1590/1676-0611-BN-2017-0452
    » http://dx.doi.org/10.1590/1676-0611-BN-2017-0452
  • PAIVA, M.P. & MESQUITA, P.E.C. 2013. Uma semente fecunda: Comissão Técnica de Piscicultura do Nordeste (1932 - 1945). Revista do Instituto do Ceará. p.10-40.
  • PAIVA, R.E.C., LIMA, S.M.Q., RAMOS, T.P.A. & MENDES, L. 2014. Fish fauna of Pratagi River coastal microbasin, extreme north Atlantic Forest, Rio Grande do Norte State, northeastern Brazil. Check List. 10(5): 968-975.
  • PITTOCK, J., MENG, J. & CHAPAGAIN, A.K. 2009. Interbasin water transfers and water scarcity in a changing world -a solution or a pipedream? A discussion paper in a burning issue, 2nd, WWF Germany, Frankfurt.
  • PYSEK, P., RICHARDSON, D.M. 2006. The biogeography of naturalization in alien plants. Journal of Biogeography 33: 2040-2050.
  • RAMOS, R.T.C., RAMOS, T.P.A., ROSA, R.S., BELTRÃO, G.B.M. & GROTH, F. 2005. Diversidade de Peixes (Ictiofauna) da bacia do rio Curimataú, Paraíba. In Análise das variações da biodiversidade do bioma caatinga: suporte das estratégias regionais de conservação (F.S. Araujo, M.J.N. Rodal & M.R.V. Barbosa, eds.). Ministério do Meio Ambiente, Brasília, p. 291-318.
  • RAMOS, T.P.A. RAMOS, R.T.C. & RAMOS, S.A.Q.A. 2014. Ichthyofauna of the Parnaíba river Basin, Northeastern Brazil. Biota Neotrop. 14(1): 1-8.
  • REASER, J.K., GALINDO-LEAL, C. & ZILLER, S.R. 2005. Visitas indesejadas: a invasão de espécies exóticas. In Mata Atlântica Biodiversidade, Ameaças e Perspectivas (C. Galindo-Leal e I.G. Câmara eds.). Fundação SOS Mata Atlântica e Conservação Internacional, Belo Horizonte. p. 392-405.
  • REIS, R.E., KULLANDER, S.O. & FERRARIS JR., C.J. 2003. Check list of the freshwater fishes of South and Central America. Editora da Pontifícia Universidade Católica do Rio Grande do Sul. Porto Alegre, Brazil.
  • RODRIGUES-FILHO, C.A.S., GURGEL-LOURENCO, R.C., BEZERRA, L.A.V., SOUSA, W.A., GARCEZ, D.S., LIMA, S.M.Q., RAMOS, T.P.A. & BOTERO, J.I.S. 2016. Ichthyofauna of the humid forest enclaves in the tablelands of Ibiapaba and Araripe, Northeastern Brazil. Biota Neotrop. (14): e20160273.
  • ROSA, R.S., MENEZES, N.A., BRITSKI, H.A., COSTA, W.J.E. & GROTH F. 2003. Diversidade, padrões de distribuição e conservação dos peixes da caatinga. In Ecologia e Conservação da Caatinga (I.R. Leal, M. Tabarelli & J.M.C. Silva eds.). Editora Universitária da Universidade Federal de Pernambuco, Recife, p.135-180.
  • SÁNCHEZ-BOTERO, J., REIS, V.C., CHAVES, F.D.N. & GARCEZ, D. 2013. Fish assemblage of the Santo Anastácio reservoir (Ceará state, Brazil). Bol. Inst. Pesca. 40(1):1-15.
  • SERRA, J.P., CARVALHO, F.R. & LANGEANI, F. 2007. Ichthyofauna of the rio Itatinga in the Parque das Neblinas, Bertioga, São Paulo: composition and biogeography. Biota Neotrop. 7(1): http://dx.doi.org/10.1590/S1676-06032007000100011
    » http://dx.doi.org/10.1590/S1676-06032007000100011
  • SILVA, L.M.T. 2003. Nas margens do Rio Paraíba do Norte. Revista Cadernos do Logepa. Série Texto Didático. Ano 2. (4).
  • SILVA, M.J., COSTA, B.G., RAMOS, T.P.A., AURICCHIO, P. & LIMA, S.M.Q. 2015. Ichthyofauna of the Gurgeia River, Parnaíba River basin, northeastern Brazil. Check List. 11: 1765.
  • SILVA, M.J., RAMOS, T.P.A., DINIZ, V.D., RAMOS, R.T.C. & MEDEIROS, E.S.F. 2014. Ichthyofauna of Seridó/Borborema: a semi-arid region of Brazil. Biota Neotrop. (14): 1-6.
  • SIMÕES, N.R., SONODA, S.L. & RIBEIRO, S.M.M.S. 2008. Spatial and seasonal variation of microcrustaceans (Cladocera and Copepoda) in intermittent rivers in the Jequiezinho River Hydrographic Basin, in the Neotropical semiarid. Acta Limnol Bras. 20(3): 197-204.
  • SHELTON, J.M., CLARK, B.M., SEPHAKA, T, TURPIE, J.K. 2016. Population crash in Lesotho's endemic Maloti minnow Pseudobarbus quathlambae following invasion by translocated smallmouth yellowfish Labeobarbus aeneus Aquatic Conservation: Marine and Freshwater Ecosystems 27: 1-13.
  • STARKS, E.C. 1913. The fishes of the Stanford Expedition to Brazil. Palo Alto: Stanford University Publications.
  • SUDENE. 1990. Superintendência do Desenvolvimento do Nordeste. Dados pluviométricos mensais do Nordeste. Recife: SUDENE, Série Pluviometria 1 a 10.
  • TEIXEIRA, F.K., RAMOS, T.P.A., PAIVA, R.E.C., TÁVORA, M.A., LIMA, S.M.Q. & REZENDE, C. F. 2017. Ichthyofauna of Mundaú river basin, Ceará State, Northeastern Brazil. Biota Neotrop. 17: p. e20160174.
  • XAVIER, R.A., DORNELLAS, C.P., MACIEL, J.S. & BÚ, J.C. 2013. Caracterização do Regime fluvial da Bacia Hidrográfica do rio Paraíba - PB, Revista Tamoios, São Gonçalo (RJ). 8(2):15-28.
  • ZA ZARSKE, A. & GÉRY, J. 1999. Revision der neotropischen Gattung Metynnis Cope, 1878. 1. Evaluation der Typusexemplare der nominellen Arten (Teleostei: Characiformes: Serrasalmidae). Zoologische Abhandlungen (Dresden). 50(2): 169-216

Publication Dates

  • Publication in this collection
    17 Sept 2018
  • Date of issue
    2018

History

  • Received
    21 Oct 2017
  • Reviewed
    15 Aug 2018
  • Accepted
    22 Aug 2018
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