Auchenipteridae belongs to the order Siluriformes and contains 25 genera and 126 species (Fricke et al., 2021) divided into two subfamilies: Centromochlinae (with nine genera) and Auchenipterinae, the latter including the species of Trachelyopterus Valenciennes, 1840 and Parauchenipterus Bleeker, 1862. Auchenipterids are small to medium-sized catfishes restricted to the Neotropical region. Several synapomorphies support the hypothesis of a monophyletic family, and its main characteristics are sexual dimorphism and internal insemination (Akama, 2004; Birindelli, 2014). Cytogenetic analyzes in this family are scarce and restricted to Ageneiosus Lacepède, 1803, Auchenipterus Valenciennes, 1840, Glanidium Lütken, 1874, Tatia Miranda Ribeiro, 1911 and Parauchenipterus (Tab. 1). Most species have 58 chromosomes (Ravedutti, Júlio, 2001; Fenocchio et al., 2008; Lui et al., 2010, 2013a), except for Ageneiosus and Tympanopleura Eigenmann, 1912 species that have 56 chromosomes (Fenocchio, Bertollo, 1992; Lui et al., 2013b), and Centromochlus heckelii (De Filippi, 1853) that has 46 chromosomes (Kowalski et al., 2020). Heterochromatin distribution pattern is located in the terminal regions of most chromosomes (Lui et al., 2010, 2015). Nucleolus Organizing Regions (NORs) are typically found on the short arm of one chromosome pair of most Auchenipteridae species studied (Lui et al., 2010, 2015). Exceptions to the most common in the group include Ageneiosus, Tympanopleura, Tatia neivai (Ihering, 1930) and Centromochlus Kner, 1858 (e.g., Fenocchio, Bertollo, 1992; Lui et al., 2013a,b; Kowalski et al., 2020). In Parauchenipterus, only P. galeatus (Linnaeus, 1766) has chromosomal data available, and all populations have 58 chromosomes (Ravedutti, Júlio, 2001; Lui et al., 2010; Araújo, Molina, 2013). However, small differences in the karyotype formula and in the AgNORs bearing pair were found. This diversity is supported by the putative chromosomal rearrangements, like pericentric inversions (Ravedutti, Júlio, 2001; Lui et al., 2009, 2010; Araújo, Molina, 2013). Moreover, according to Araújo, Molina (2013), this species is likely a species complex.
The lack of morphological diversity causes confusion in taxonomic classification in some fish groups and makes systematic organization difficult (for review, see Keat-Chuang Ng et al., 2017). The validation of Parauchenipterus has been the subject of extensive discussion for over two centuries, which has been considered valid by some researchers (Curran, 1989; Royero, 1999; Akama, 2004; Buckup et al., 2007; Graça, Pavanelli, 2007). Akama (2004) attempted to sort it out and pondered this genus valid, dividing it into two groups: “galeatus group”, composed of Parauchenipterus sp. n. and P. galeatus, which would have wide distribution occurring in the Amazon, Orinoco, Paraná-Paraguay, Guyana, São Francisco and Northeast Brazil drainages; and “striatulus group”, composed by Parauchenipterus ceratophysus (Kner, 1858), Parauchenipterus striatulus (Steindachner, 1877)and Parauchenipterus porosus (Eigenmann & Eigenmann, 1888), distributed in the Amazon basin, Paraná-Paraguay basin, drainages from eastern Brazil and possibly in the northeastern of Brazil. This classification was based on differences of osteological characters and male gonadal apparatus. Even though some researchers disagree with the validity of Parauchenipterus, following studies to the review by Akama (2004), suggest that Parauchenipterus is synonym of Trachelyopterus (Ferraris, 2007; Birindelli, 2014; Calegari et al., 2019).
The taxonomic conflict between Parauchenipterus and Trachelyopterus is due to the great morphological similarity between these two nominal genera. Therefore, three species of these genera were cytogenetically analyzed (P. striatulus from Doce River basin, and P.galeatus and Trachelyopteruscoriaceus Valenciennes, 1840 from Araguaia River basin) to highlight the historical taxonomic problematic linked to this group of Neotropical fishes. In addition, the present work attempt to contribute to the taxonomic problem of Parauchenipterus, analyzing species from the “galeatus group” and “striatulus group”. These groups were defined in the last research, which focused in discussing Parauchenipterus validation (Akama, 2004), what did not happen until now.
Material and methods
Individuals of Parauchenipterus striatulus (7 males 5 females) were collected in Verde Lake, Doce River basin in Mariléia city, Minas Gerais State, Brazil, 19º49’44.5”S 42º37’52.5”W. Parauchenipterus galeatus (9 males 10 females) and Trachelyopterus coriaceus (6 males 9 females) were collected from the Marginal Lake to the Córrego do Medo, tributary of the Araguaia River in São Miguel do Araguaia city, Ana Maria farm, Goiás State, Brazil, 13º08’52.7”S 50º25’02.8”W, with fishing nets (Permanent License SISBIO 10538-1). The specimens were kept in aquaria and subsequently euthanized by clove oil overdose (Griffiths, 2000; Pereira-Da-Silva et al., 2009) (according to the Animal Experimentation Ethics Committee and Unioeste practical classes: 13/09 – CEEAAP/Unioeste), to remove tissues for cytogenetic preparations. The collected specimens were deposited in the Museu de Zoologia da Universidade de São Paulo, São Paulo, under the voucher numbers: MZUSP 109798 for P. striatulus, MZUSP 109793 and 110803 for P. galeatus, and MZUSP 106766 for T. coriaceus.
TABLE 1 | Cytogenetic data in Auchenipteridae. FN: fundamental number; 2n: diploid number; Res.: Reservoir; m: metacentric; sm: submetacentric; st: subtelocentric; a: acrocentric; p: short arm; q: long arm; W: sex chromosome. References (Ref.): 1. Ravedutti, Júlio (2001); 2. Fenocchio et al. (2008); 3. Lui et al. (2015); 4. Lui et al. (2013a); 5. Kowalski et al. (2020); 6. Fenocchio, Bertollo (1992); 7. Lui et al. (2013b); 8. Lui et al. (2010); 9. Araújo, Molina (2013); 10. Present study.
Metaphasic mitotic chromosomal cell suspensions were prepared with anterior kidney cells (Bertollo et al., 1978; Foresti et al., 1993). The best metaphases were selected for karyotyping. Chromosomal morphology was determined according to Levan et al. (1964). The heterochromatin distribution pattern was determined according to Sumner (1972) with modifications in the staining process (Lui et al., 2012). Nucleolus organizing regions (AgNORs) were identified using silver nitrate (AgNO3) staining (Howell, Black, 1980). Both heterochromatin and NOR detection methods were carried out after Giemsa staining in order to follow a sequential analysis. Fluorescent in situ Hybridization (FISH) with 18S ribosomal (rDNA) and 5S rDNA probes was performed under stringency of 77% and followed the method by Pinkel et al. (1986), with modifications suggested by Margarido, Moreira-Filho (2008). 5S rDNA and 18S rDNA probes were obtained by DNA from Leporinuselongatus Valenciennes, 1850 (Martins, Galetti, 1999) and Prochilodusargenteus Spix & Agassiz, 1829 (Hatanaka, Galetti, 2004), respectively. Probes were labeled by nick translation with digoxigenin-11-dUTP (18S rDNA for P. striatulus; 5S rDNA for P. galeatus, and T. coriaceus) and biotin-16-dUTP (5S rDNA for P. striatulus; 18S rDNA for P. galeatus, and T. coriaceus), in accordance with the manufacturer’s instructions (Roche). Chromosomes were counterstained with DAPI (50 μg/mL). The slides were photographed through BX61 epifluorescence microscope (Olympus America Inc., Center Valley, PA, United States of America) with an attached Olympus DP71 digital camera and DP Controller 126.96.36.1996 software.
Parauchenipterus striatulus: Doce River basin. Diploid number (2n) was 58 chromosomes and the karyotype was composed of 18 metacentric, 20 submetacentric, 10 subtelocentric, and 10 acrocentric chromosomes (Fig. 1A). AgNO3 staining demonstrated simple NORs allocated in terminal region on the short arm of the submetacentric pair 23 (Fig. 1A, in box). C-banding technique evidenced pale heterochromatin in terminal regions of almost all chromosome pairs (Fig. 1D). 18S rDNA-FISH confirmed previous findings by AgNO3 staining and revealed these sequences only on pair 23. 5S rDNA-FISH detected these sequences in three submetacentric pairs, on the short arm of the pair 10 and 13, and on the long arm of the pair 15 (Fig. 1G).
Parauchenipterus galeatus: Araguaia River basin. Diploid number was 58 chromosomes and karyotype was composed of 20 metacentric, 18 submetacentric, 12 subtelocentric, and 8 acrocentric (Fig. 1B). AgNO3 staining revealed simple NORs allocated in the terminal region on the short arm of the submetacentric pair 24 (Fig. 1B, in box). C-banding evidenced pale heterochromatin in terminal regions of almost all chromosome pairs (Fig. 1E). 18S rDNA-FISH confirmed previous finding by AgNO3 staining, simple NORs on pair 24. 5S rDNA-FISH detected these sites on short arm of the metacentric chromosome pair 3 (Fig. 1H).
Trachelyopterus coriaceus: Araguaia River basin. Diploid number was 58 chromosomes and karyotype was composed of 20 metacentric, 18 submetacentric, 12 subtelocentric, and 8 acrocentric (Fig. 1C). AgNO3 staining revealed simple NORs allocated in terminal region on the short arm of the submetacentric chromosome pair 23 (Fig. 1C, in box). C-banding evidenced pale heterochromatin in terminal regions on almost all karyotype pairs (Fig. 1F). 18S rDNA-FISH also revealed only the pair 23 with these sites, corresponding to what was evidenced by the AgNO3. 5S rDNA-FISH probe detected these sites on the short arm of the metacentric pair 3 and on the long arm of the submetacentric pair 16 (Fig. 1I).
FIGURE 1 | Karyotypes of A. Parauchenipterusstriatulus, B. Parauchenipterusgaleatus and C. Trachelyopteruscoriaceus. Giemsa stained karyotypes. The chromosome pairs marked with silver nitrate are in the boxes; D, E, F. C-banding sequentially karyotypes; G, H, I. Karyotypes hybridized with 5S rDNA and 18S rDNA probes. G. rDNA probe 18S (rhodamine, red signal), 5S rDNA probe (FITC, green signal). H, I. rDNA probe 18S (FITC, green signal), 5S rDNA probe (rhodamine, red signal).
The same diploid number of 58 chromosomes was found in all three species analyzed herein, which is considered basal for Auchenipteridae (Lui et al., 2013a, 2015), due to its prevalence within the species with available chromosome data (Tab. 1) and mainly because cytogenetic data in Doradidae (e.g., Eler et al., 2007; Milhomem et al., 2008; Baumgärtner et al., 2016; Takagui et al., 2017, 2019), sister-group of Auchenipteridae (Sullivan et al., 2006; Nelson et al., 2016). According Takagui et al. (2019), the most probable ancestor karyotype in Doradidae had 58 chromosomes. Ageneiosus inermis (Linnaeus, 1766) (Fenocchio, Bertollo, 1992; Lui et al., 2013b), Tympanopleura atronasus (Eigenmann & Eigenmann, 1888) (cited as A. atronasus) (Fenocchio, Bertollo, 1992) and C. heckelii (Kowalski et al., 2020) are exceptions, because they have lower diploid numbers. These reduced diploid numbers are probably result of fusion events (Lui et al., 2013b; Kowalski et al., 2020), which were confirmed by the presence of ITS (Interstitial Telomeric Sequence) in a metacentric chromosome pair detected in A. inermis (Lui et al., 2013b).
Small karyotype formula differences are found among the species analyzed in the present study. Parauchenipterus striatulus has higher amount of acrocentric (10 chromosomes) than P. galeatus and T. coriaceus (8 chromosomes). The presence of eight acrocentric chromosomes has already been reported in other three populations of P. galeatus (Lui et al., 2010), and their karyotype formulas are also very similar to the population from this study. Therefore, it shows irrelevant karyotype variation between these taxa, and these karyotype differences might be related to non-Robertsonian events, which do not imply diploid number changes. Nonetheless, the population of P. galeatus from Porto Rico in the Paraná River had 18 acrocentric chromosomes, and this difference is probably related to methodological problems, such as the chromosomal condensation pattern, which difficult the classification of chromosomes by different researchers, as already proposed for other fish groups (e.g., Carvalho, Dias 2005; Moraes-Neto et al., 2011). The two sympatric species (P. galeatus and T. coriaceus) had the same karyotype formula that indicates large chromosomal similarity between these two species. Moreover, researchers suggest that these species belong to different genera, supported by morphological data, as initially considered in this paper by Akama (2004); however, these chromosomal data reinforce the phylogenetic closeness between these two nominal genera.
Heterochromatin distribution was similar among the three analyzed species. Pale heterochromatin was found in terminal region of almost all chromosomes, as observed in other P.galeatus populations (Ravedutti, Júlio, 2001; Lui et al., 2009, 2010).
This pattern is typically found in other Auchenipteridae species, such as Ageneiosus inermis (cited as A. brevifilis), Tympanopleura atronasus (cited as A. atronasus), Auchenipterus osteomystax (Miranda-Ribeiro, 1918) (cited as A. nuchalis), and Glanidium ribeiroi Haseman, 1911 (Fenocchio, Bertollo, 1992; Ravedutti, Júlio, 2001; Fenocchio et al., 2008; Lui et al., 2013b, 2015), suggesting to be a common family trait. On the other hand, small differences are found in some of these species: heterochromatin in terminal regions is strongly reported for A. inermis (Lui et al., 2013b); heterochromatin in centromeric region of chromosomes is observed for Tatia jaracatia Pavanelli & Bifi, 2009, and a conspicuous block in the interstitial region of a submetacentric pair is reported for T. neivai (Lui et al., 2013a).
AgNO3 impregnation and FISH with 18S rDNA probe evidenced simple NORs in the terminal position on a subtelocentric pair 23 in P. galeatus and P. striatulus, and on a subtelocentric pair 24 in T. coriaceus. According to Ravedutti, Júlio (2001), simple NORs may be a common characteristic of Auchenipteridae, which has been confirmed by recent studies on this family (Tab. 1). Even though only one chromosomes pair bearing NORs is found in almost all auchenipterids, the location varies (terminal and interstitial), due to pericentric inversions, as aforementioned to explain the differences between karyotypic formulas. The three species in this study also had 18S rDNA present in subtelocentric chromosomes, as in most P. galeatus populations studied (Lui et al., 2009, 2010), however, there are populations with this marker located either in a pair of acrocentric (Ravedutti, Júlio, 2001) or submetacentric chromosomes (Araújo, Molina, 2013). As mentioned above, these differences might be associated with different chromatin condensation levels, which hinder their classification by researchers. Moreover, by analyzing the karyotypes of these last two papers, the pair bearing the NORs could have been classified as subtelocentric.
Despite the conservatism in the number of 18S rDNA sites for this family and small variation in the bearing pair, 5S rDNA has been found to be the chromosomal marker with the highest variability among Auchenipteridae species (Tab. 1). 5S rDNA has shown to be more dynamic, also evident in the data presented in this study. These cistrons were found in only one pair of chromosomes in G. ribeiroi and A. inermis (Lui et al., 2013b, 2015), but multiple 5S rDNA is more prevalent in the species of the genus Tatia: four pairs in T. jaracatia (metacentric pair 4, submetacentric pairs 18 and 19, and subtelocentric pair 29) and three pairs in T. neivai (metacentric pair 4 and submetacentric pairs 21 and 22) (Lui et al., 2013a). 5S rDNA submetacentric pairs reported for Tatia and Parauchenipterus species can be considered corresponding to the submetacentric pairs found in the species of this study, as they have similar measures, morphology, and position. Physical mapping of rDNA is considered a promising implement for evolutionary and taxonomic analyzes in fishes (Moraes-Neto et al., 2011), and the three species analyzed in this study indicate variation in the number of 5S rDNA bearing chromosome pairs. Therefore, this marker seems to be remarkable to understand chromosomal evolution of Auchenipteridae.
Regarding 5S rDNA data in Parauchenipterus and Trachelyopterus, FISH made it possible to identify differences among the three species of this paper. There are similar results found in other populations of P. galeatus, from different watersheds and all of these populations have two 5S rDNA submetacentric pairs (Lui et al., 2010). Trachelyopterus coriaceus also has two chromosome pairs carrying 5S rDNA sites, one metacentric and one submetacentric. Even though the morphology of these chromosomes is different from the two pairs of Parauchenipterus, these chromosomes can be considered corresponding. Similarly, P. striatulus also has two chromosomes (one with these clusters on short arm and the other one on the long arm) that might be corresponding to the same pairs. Moreover, the extra third 5S rDNA carrier submetacentric pair of P. striatulus, can be considered an autapomorphy of this species. It confirms that 5S rDNA is a good marker for the group, because these data differentiate P. striatulus from other phylogenetically close species. It is important to highlight that this species has distribution in coastal basins of the South American continent, different from P. galeatus and T. coriaceus, which are present in basins in the interior of the continent, thus there is no overlap in distribution and it suggests ancient diversification of P. striatulus from the other Trachelyopterus and explains the exclusive third 5S rDNA chromosome pair of this species.
Comparison of 5S rDNA distribution data among all populations of P. galeatus previously studied, T. coriaceus and P. striatulus shows greater similarity between P. galeatus from Araguaia River and T. coriaceus than with other P. galeatus populations. At a minimum, these data reinforce the phylogenetic proximity between these two nominal genera, and may even give rise to an interpretation contrary to Parauchenipterus validation. Thus, the differences in P. galeatus 5S rDNA data from Araguaia River basin, regarding the variation in number of sites from all other populations in this group, and the greater similarity with the sympatric population of T. coriaceus make it possible to suggest the existence of a new taxonomic unity. According to Birindelli et al. (2012), Trachelyopterus can be diagnosed by its gas bladder morphology among other characters. Trachelyopterus galeatus specimens analyzed showed differences in the gas bladder morphology (Birindelli et al., 2012), which could be interpreted as an indicative of cryptic diversity. Our data also suggest a population as a potentially new taxon in this fish group.
Considering the proposal of Akama (2004), the species belonging to Trachelyopterus analyzed in this study are the first report of cytogenetic data for this genus, and also the first record for a P.striatulus population. Comparing the data of Parauchenipterus and Trachelyopterus described here with those already found in the literature, it is possible to note the great similarity concerning chromosomal markers (diploid number, heterochromatin distribution, number and location of nucleolus organizing regions) and differences in 5S rDNA number and location. This way, our data reaffirm that Parauchenipterus should be considered synonymous of Trachelyopterus, contrary to what was suggested by last diagnosis reviewed of Parauchenipterus and closely related species (Akama, 2004), but in agreement with some other more recent studies in Auchenipteridae that were not focused on this issue (Ferraris, 2007; Birindelli, 2014; Calegari et al., 2019). It is noteworthy that maintaining Parauchenipterus as a junior synonym of Trachelyopterus is based on the greatest similarity between the sympatric species P.galeatus and T. coriaceus, compared to all others Auchenipteridae previously studied, mainly Trachelyopterus species, through the following chromosomal data: equal karyotype formula and metacentric pair 3 with marking on the short arm bearing rDNA 5S (for more detail, see Tab. 1). The 5S rDNA is an excellent marker to understand chromosomal evolution of Auchenipteridae and helped to suggest the existence of a new taxonomic unit distributed in the Araguaia River basin, which reaffirms the status of species complex in P. galeatus.
We are grateful to Dr. Heraldo Antonio Britski (MZUSP) and Dr. José Luís Olivan Birindelli (MZUEL) for the identification of the specimens; to the laboratory technicians Pedro Luis Gallo and Luis Henrique da Silva for their assistance in sampling; to Chico Mendes Institute for Biodiversity Conservation (Permit number 10538–1) for authorizing the collection of the specimens; to Minas Gerais State Forestry Institute for assisting the specimens collections in the state (Rio Doce State Park); and to Sr. Osmar Pereira de Barros, owner of the Ana Maria farm in São Miguel do Araguaia, who helped us to collect the fishes in this region. This study was funded by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and Fundação Araucária de Apoio ao Desenvolvimento Científico e Tecnológico do Estado do Paraná (FA).
Akama A. Sistemática dos gêneros Parauchenipterus Bleeker, 1862 e Trachelyopterus Valenciennes, 1840 (Siluriformes, Auchenipteridae). [PhD Thesis]. São Paulo: Universidade de São Paulo; 2004.
Araújo WC, Molina WF. Citótipo exclusivo para Parauchenipterus galeatus (Siluriformes, Auchenipteridae) na Bacia do Atlântico NE Oriental do Brasil: Indicações de um complexo de espécies. Biota Amazon. 2013; 3(2):33–39. http://dx.doi.org/10.18561/2179-5746/biotaamazonia.v3n2p33-39
Baumgärtner L, Paiz LM, Margarido VP, Portela-Castro ALB. Cytogenetics of the Thorny Catfish Trachydoras paraguayensis (Eigenmann & Ward, 1907), Siluriformes, Doradidae): Evidence of pericentric inversions and chromosomal fusion. Cytogenet Genome Res. 2016; 149(3):201–06. https://doi.org/10.1159/000448126
Bertollo LAC, Takahashi CS, Moreira-Filho O. Cytotaxonomic consideration on Hoplias lacerdae (Pisces, Erythrinidae). Rev Bras Genet. 1978; 1:103–20.
Birindelli JLO. Phylogenetic relationships of the South American Doradoidea (Ostariophysi: Siluriformes). Neotrop Ichthyol. 2014; 12(3):451–564. http://dx.doi.org/10.1590/1982-0224-20120027
Birindelli JLO, Akama A, Britski HA. Comparative morphology of the gas bladder in driftwood catfishes (Silurformes: Auchenipteridae). J Morphol. 2012; 273(6):651–60. https://doi.org/10.1002/jmor.20012
Buckup PA, Menezes NA, Guazzi MS, editors. Catálogo das espécies de peixes de água doce do Brasil. Rio de Janeiro: Museu Nacional; 2007.
Calegari BB, Vari RP, Reis RE. Phylogenetic systematics of the driftwood catfishes (Siluriformes: Auchenipteridae): a combined morphological and molecular analysis. Zool J Linn Soc. 2019; 187(3):661–773. https://doi.org/10.1093/zoolinnean/zlz036
Carvalho RA, Dias AL. Cytogenetic characterization of B chromosomes in two populations of Iheringichthys labrosus (Pisces, Pimelodidae) from the Capivara reservoir (Parana, Brazil). Caryologia G Citol Citosistematica Citogenet. 2005; 58(3):269–73. https://doi.org/10.1080/00087114.2005.10589462
Curran DJ. Phylogenetic relationships among the catfish genera of the family Auchenipteridae (Teleostei: Siluroidea). Copeia. 1989; 1989(2):408–19. https://doi.org/10.2307/1445438
Eler ES, Dergam JA, Vênere PC, Paiva LC, Miranda GA, Oliveira AA. The karyotypes of the thorny catfishes Wertheimeria maculata Steindachner, 1877 and Hassar wilderi Kindle, 1895 (Siluriformes, Doradidae) and their relevance in doradids chromosomal evolution. Genetica. 2007; 130(1):99–103. https://doi.org/10.1007/s10709-006-0023-4
Fenocchio AS, Bertollo LAC. Karyotype, C-bands and NORs of the neotropical siluriform fish Ageneiosus brevifilis and Ageneiosus atronases (Ageneiosidae). Cytobios. 1992; 72(288):19–22.
Fenocchio AS, Dias AL, Margarido VP, Swarça AC. Molecular cytogenetic characterization of Glanidium ribeiroi (Siluriformes) endemic to the Iguaçu River. Brazil. Chromosome Sci. 2008; 11:61–66.
Ferraris CJ Jr. Checklist of catfishes, recent and fossil (Osteichthyes: Siluriformes), and catalogue of siluriform primary types. Zootaxa. 2007; 1418(1):1–628. https://doi.org/10.11646/zootaxa.1418.1.1
Foresti F, Oliveira C, Almeida-Toledo LF. A method for chromosome preparations from large fish specimens using in vitro short-term treatment with colchicines. Experientia. 1993; 49:810–13. https://doi.org/10.1007/BF01923555
Fricke R, Eschmeyer WN, Fong JD. Eschmeyer’s catalog of fishes: species by family/subfamily [Internet]. San Francisco: California Academy of Sciences; 2021. Available from: http://researcharchive.calacademy.org/research/ichthyology/catalog/SpeciesByFamily.asp
Graça WJ, Pavanelli CS. Peixes de planície de inundação do Alto rio Paraná e áreas adjacentes. Maringá: EDUEM; 2007.
Griffiths SP. The use of clove oil as an anaesthetic and method for sampling intertidal rockpool fishes. J Fish Biol. 2000; 57(6):1453–64. https://doi.org/10.1111/j.1095-8649.2000.tb02224.x
Hatanaka T, Galetti PM. Mapping of the 18S and 5S ribossomal RNA genes in the fish Prochilodus argenteus Agassiz, 1829 (Characiformes, Prochilodontidae). Genetica. 2004; 122(3):239–44. https://doi.org/10.1007/s10709-004-2039-y
Howell WM, Black DA. Controlled silver-staining of nucleolus organizer regions with a protective colloidal developer: A 1-step method. Experientia. 1980; 6:1014–15. https://doi.org/10.1007/BF01953855
Keat-Chuang Ng C, Aun-Chuan Ooi P, Wong WL, Khoo G. A review of fish taxonomy conventions and species identification techniques. J Surv Fish Sci. 2017; 4(1):54–93. https://doi.org/10.18331/SFS2017.4.1.6
Kowalski S, Paiz LM, Silva M, Machado AS, Feldberg E, Traldi JB, Margarido VP, Lui RL. Chromosomal analysis of Centromochlus heckelii (Siluriformes: Auchenipteridae), with a contribution to Centromochlus definition. Neotrop Ichthyol. 2020; 18(3):e200009. https://doi.org/10.1590/1982-0224-2020-0009
Levan A, Fredga K, Sandberg AA. Nomenclature for centromeric position on chromosomes. Hereditas. 1964; 52(2):201–20. https://doi.org/10.1111/j.1601-5223.1964.tb01953.x
Lui RL, Blanco DR, Margarido VP, Moreira-Filho O. First description of B chromosomes in the family Auchenipteridae, Parauchenipterus galeatus (Siluriformes) of the São Francisco river basin (MG, Brazil). Micron. 2009; 40(5–6):552–59. https://doi.org/10.1016/j.micron.2009.03.004
Lui RL, Blanco DR, Margarido VP, Moreira-Filho O. Chromosome characterization and biogeographic relations among three populations of the driftwood catfish Parauchenipterus galeatus (Linnaeus, 1766) (Siluriformes: Auchenipteridae) in Brazil. Biol J Linn Soc Lond. 2010; 99(3):648–56. https://doi.org/10.1111/j.1095-8312.2009.01389.x
Lui RL, Blanco DR, Margarido VP, Troy WP, Moreira-Filho O. Comparative chromosomal analysis and evolutionary considerations concerning two species of genus Tatia (Siluriformes, Auchenipteridae). Comp Cytogenet. 2013a; 7(1):63–71. https://doi.org/10.3897/CompCytogen.v7i1.4368
Lui RL, Blanco DR, Martinez JF, Margarido VP, Venere PC, Moreira-Filho O. The role of chromosomal fusion in the karyotypic evolution of the genus Ageneiosus (Siluriformes, Auchenipteridae). Neotrop Ichthyol. 2013b; 11(2):327–34. https://doi.org/10.1590/S1679-62252013005000004
Lui RL, Blanco DR, Moreira-Filho O, Margarido VP. Propidium iodide for making heterochromatin more evident in the C-banding technique. Biotech Histochem. 2012; 87(7):433–38. https://doi.org/10.3109/10520295.2012.696700
Lui RL, Blanco DR, Traldi JB, Margarido VP, Moreira-Filho O. Karyotypic variation of Glanidium ribeiroi Haseman, 1911 (Siluriformes, Auchenipteridae) along the Iguazu river basin. Braz J Biol. 2015; 75(4):215–21. https://doi.org/10.1590/1519-6984.10714
Margarido VP, Moreira-Filho O. Karyotypic differentiation through chromosome fusion and number reduction in Imparfinis hollandi (Ostariophysi, Heptapteridae). Genet Mol Biol. 2008; 31(1):235–38. https://doi.org/10.1590/S1415-47572008000200012
Martins C, Galetti PM Jr. Chromosomal localization of 5S rDNA genes in Leporinus fish (Anostomidae, Characiformes). Chromosome Res. 1999; 7:363–67. https://doi.org/10.1023/A:1009216030316
Milhomem SSR, Souza ACP, Nascimento AL, Carvalho JR Jr., Feldberg E, Pieczarka JC, Nagamachi CY. Cytogenetic studies in fishes of the genera Hassar, Platydoras and Opsodoras (Doradidae, Siluriformes) from Jarí and Xingú Rivers, Brazil. Genet Mol Biol. 2008; 31(1):256–60. https://doi.org/10.1590/S1415-47572008000200017
Moraes-Neto A, Silva M, Matoso DA, Vicari MR, Almeida MC, Collares-Pereira MJ, Artoni RF. Karyotype variability in neotropical catfishes of the family Pimelodidae (Teleostei: Siluriformes). Neotrop Ichthyol. 2011; 9(1):27–105. https://doi.org/10.1590/S1679-62252011005000002
Nelson JS, Grande TC, Wilson MVH, editors. Fishes of the world. Hoboken: John Wiley & Sons; 2016.
Pereira-Da-Silva EM, Oliveira RHF, Ribeiro MAR, Coppola MP. Efeito anestésico do óleo de cravo em alevinos de lambari. Cienc Rural. 2009; 39(6):1851–56. https://doi.org/10.1590/S0103-84782009005000127
Pinkel D, Straume T, Gray JW. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc Natl Acad Sci U S A. 1986; 83(9):2934–38. https://doi.org/10.1073/pnas.83.9.2934
Ravedutti CG, Júlio HF Jr. Cytogenetic analysis of three species of the neotropical family Auchenipteridae (Pisces, Siluriformes) from the Paraná river basin, Brazil. Cytologia. 2001; 66(1):65–70. https://doi.org/10.1508/cytologia.66.65
Royero RL. Studies on the systematics and phylogeny of the catfish family Auchenipteridae (Teleostei: Siluriformes). [PhD Thesis]. Bristol: University of Bristol; 1999.
Sullivan JP, Lundberg JG, Hardman M. A phylogenetic analysis of the major groups of catfishes (Teleostei: Siluriformes) using rag1 and rag2 nuclear gene sequences. Mol Phylogenet Evol. 2006; 41(3):636–62. https://doi.org/10.1016/j.ympev.2006.05.044
Sumner AT. A simple technique for demonstrating centromeric heterochromatin. Exp Cell Res. 1972; 75(1):304–06. https://doi.org/10.1016/0014-4827(72)90558-7
Takagui FH, Moura LF, Ferreira DC, Centofante L, Vitorino CA, Bueno V, Margarido VP, Venere PC. Karyotype diversity in Doradidae (Siluriformes, Doradoidea) and presence of the heteromorphic ZZ/ZW sex chromosome system in the family. Zebrafish. 2017; 14(3):236–43. https://doi.org/10.1089/zeb.2016.1368
Takagui FH, Baumgärtner L, Baldissera JN, Lui RL, Margarido VP, Fonteles SBA, Garcia C, Birindelli JO, Moreira-Filho O, Almeida FS, Giuliano-Caetano L. Chromosomal diversity of thorny catfishes (Siluriformes-Doradidae): a case of allopatric speciation among Wertheimerinae species of São Francisco and Brazilian Eastern Coastal Drainages. Zebrafish. 2019; 16(5):477–85. https://doi.org/10.1089/zeb.2019.1769
 Universidade Estadual do Oeste do Paraná, Centro de Ciências Biológicas e da Saúde, R. Universitária, 1619, Universitário, 85819-170 Cascavel, PR, Brazil. (DPS) firstname.lastname@example.org; (DF) email@example.com; (LB) firstname.lastname@example.org; (VMP) email@example.com; (RLL) firstname.lastname@example.org (corresponding author)
Dayane Petik dos Santos: Data curation, Investigation, Methodology, Writing-original draft.
Denise Felicetti: Investigation, Methodology, Writing-original draft, Writing-review and editing.
Lucas Baumgärtner: Formal analysis, Investigation, Methodology, Writing-original draft, Writing-review and editing.
Vladimir Pavan Margarido: Conceptualization, Data curation, Formal analysis, Funding acquisition, Resources, Supervision, Writing-original draft, Writing-review and editing.
Daniel Rodrigues Blanco: Conceptualization, Data curation, Investigation, Methodology, Writing-original draft, Writing-review and editing.
Orlando Moreira-Filho: Conceptualization, Project administration, Writing-original draft.
Roberto Laridondo Lui: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Writing-original draft, Writing-review and editing.
Permanent License SISBIO 10538-1. The specimens were kept in aquaria and subsequently euthanized by clove oil overdose (Griffiths, 2000; Pereira-Da-Silva et al., 2009) (according to the Animal Experimentation Ethics Committee and Unioeste practical classes: 13/09 – CEEAAP/Unioeste).
The authors declare no competing interests.
How to cite this article
Santos DP, Felicetti D, Baumgärtner L, Margarido VP, Blanco DR, Moreira-Filho O, Lui RL. Contributions to the taxonomy of Trachelyopterus (Siluriformes): comparative cytogenetic analysis in three species of Auchenipteridae. Neotrop Ichthyol. 2021; 19(1):e200115. https://doi.org/10.1590/1982-0224-2020-0115
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Creative Commons CC-BY 4.0
© 2021 The Authors.
Diversity and Distributions Published by SBI
Submitted October 15, 2020
Accepted February 10, 2021
by Carlos Do Nascimiento
Epub March 31, 2021