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Camilla B Di-Nizo, Ana Lazar, Carlos A Cunha-Filho, Maria José J Silva, Alexandra M R Bezerra, Elkin Y Suárez-Villota, Cibele R Bonvicino, Leila M Pessôa, Pablo R Gonçalves, Species limits in Wiedomys (Cricetidae: Sigmodontinae) reinforce the South American São Francisco River as a biogeographic barrier, Journal of Mammalogy, Volume 106, Issue 1, February 2025, Pages 2–29, https://doi.org/10.1093/jmammal/gyae129
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Abstract
Red-nosed mice (genus Wiedomys) are restricted to the Brazilian Cerrado and Caatinga biomes, distributed along the São Francisco River (SFR). Until recently, Wiedomys was considered monotypic, but 2 species with poorly defined geographic and morphological limits have been recognized: W. cerradensis and W. pyrrhorhinos. Our study used morphological, phylogenetic, and cytogenetic analyses to review and detail species limits within the genus and test whether the SFR could be associated with divergence between lineages. This integrative approach indicated that the SFR delineates the geographic boundaries between species, with W. pyrrhorhinos on the right bank and W. cerradensis on the left bank. The species are reciprocally monophyletic and diverge in cranial size, nasal morphology, and facial pelage color pattern. Karyotypic differences between and within W. pyrrhorhinos and W. cerradensis were also detected, and new chromosome complements (2n = 62, FN = 96 and 2n = 62, FN = 88, respectively) were found. Divergence time (0.339 to 0.025 Ma) is concordant with the timing of diversification of other co-distributed vertebrate taxa, and close to a younger estimate for the formation of SFR’s recent lower course to the east coast. Therefore, our study considerably expands knowledge of the geographic range of the genus, diagnoses of species, karyotypic variability between and within species, and reinforces the role of SFR as an important vicariant barrier in northeastern Brazil.
Resumo
Os ratos-bico-de-lacre (gênero Wiedomys) estão restritos aos biomas brasileiros do Cerrado e da Caatinga, distribuídos ao longo do rio São Francisco (RSF). Até recentemente, Wiedomys era considerado monotípico, mas duas espécies com limites geográficos e morfológicos pouco detalhados foram reconhecidas: W. cerradensis e W. pyrrhorhinos. No presente estudo, tivemos como objetivo revisar e detalhar os limites das espécies dentro do gênero e testar se o RSF poderia estar associado à divergência entre as linhagens, usando análises morfológicas, filogenéticas e citogenéticas. Esta abordagem integrativa indicou que o RSF é concordante com os limites geográficos das duas espécies, com W. pyrrhorhinos na margem direita e W. cerradensis na margem esquerda. As espécies são reciprocamente monofiléticas e divergem quanto ao tamanho do crânio, morfologia nasal e padrão de coloração da pelagem facial. Diferenças cariotípicas entre e dentro de W. pyrrhorhinos e W. cerradensis também foram detectadas, e novos complementos cromossômicos (2n = 62, NF = 96 e 2n = 62, NF = 88, respectivamente) foram reportados. O tempo de divergência (0,339-0,025 Ma) é concordante com eventos de diversificação em outros táxons de vertebrados co-distribuídos e se aproxima à estimativa mais recente para a formação do baixo curso do RSF. Portanto, nosso estudo expande consideravelmente o conhecimento sobre as distribuições geográficas do gênero, as diagnoses das espécies e suas variabilidades cariotípicas, e também indica o RSF como uma potencial barreira vicariante para o gênero Wiedomys no Nordeste do Brasil.
The open-dry vegetation formations of central and eastern South America, also referred to as the dry diagonal, extend across a broad latitudinal range that comprises the Chaco, Cerrado, and Caatinga biomes (Prado 2000; Werneck 2011; Silva et al. 2017). The Cerrado is the largest open vegetation biome of South America, forming a savanna that covers an area of approximately 20% of the Brazilian territory, with small enclaves in Bolivia (Werneck et al. 2012). This biome is considered an important center of endemism in South America (Cracraft 1985; Myers et al. 2000), bearing diverse physiognomies, from gallery and riverine forests to shrublands and grasslands (Eiten 1983; Oliveira-Filho and Ratter 2002; Werneck 2011). The Caatinga is the largest and isolated nucleus of Seasonally Dry Tropical Forests (Werneck 2011; Silva et al. 2017), restricted to northeastern Brazil, and characterized by deciduous and xerophilous vegetation adapted to a semiarid climate (Rizzini 1979; Barreto 1996; Ab’Sáber 1998). Both biomes are crossed by long and broad rivers, and they harbor high levels of diversity and endemism, especially for small terrestrial vertebrates such as rodents, snakes, and lizards (Rodrigues 1992, 1996; Rocha 1995; Carmignotto et al. 2012; Gutiérrez and Marinho-Filho 2017).
Large rivers may act as important dispersal barriers leading to lineage diversification (Patton et al. 1994, 2000; Peres et al. 1996; Gascon et al. 2000; Moritz et al. 2000), and their biogeographical significance has been recognized since, at least, the work of the British naturalist Alfred R. Wallace on Amazonian rivers (Wallace 1854). In northeastern Brazil, the São Francisco River is the largest and longest watercourse, flowing along 2,700 km and crossing portions of Caatinga, Cerrado, and the Atlantic Forest. It is the second largest river in Brazil (Kohler 2003) and was probably formed in the Late Cretaceous, approximately 65 million years ago (Potter 1997), presenting opportunities for a dynamic biogeographic history throughout the Cenozoic (Werneck et al. 2015). Biogeographical studies of the open diagonal biotas have suggested that the São Francisco River represents a barrier to gene flow for some vertebrate taxa. However, as recognized previously by other researchers working on Amazonian rivers (Peres et al. 1996; Gascon et al. 2000; Moritz et al. 2000; Patton et al. 2000), testing the riverine hypothesis is challenging. For one, river courses can be highly dynamic over long and short timescales. Thus, geographic data alone cannot distinguish between the hypotheses of rivers as secondary barriers limiting the distribution of lineages that diverged elsewhere or as primary vicariant barriers that promoted speciation. With the latter hypothesis, we would expect congruence among nonvolant and nonaquatic taxa in the age and location of divergence. Therefore, testing the biogeographic role of the São Francisco River requires the study of many taxa widely distributed across the Cerrado and Caatinga biomes. For many taxa in this region, taxonomic and biogeographic revisions are needed—Red-nosed mice of genus Wiedomys are a prime example.
WiedomysHershkovitz, 1959 is one of the few rodent genera of the subfamily Sigmodontinae restricted to the Cerrado and Caatinga biomes in Brazil (Bonvicino 2015). The evolutionary uniqueness of this genus was recognized by Reig (1980), who created the tribe Wiedomyini to include it as the sole extant taxon, along with the Pliocene fossil Cholomys pearsoni. The contents of this tribe have been recently revised and the living genera Juliomys, Phaenomys, and Wilfredomys were included as its additional members (Pardiñas et al. 2014; Machado et al. 2015; Gonçalves et al. 2020), while the fossil C. pearsoni and W. marplatensis have been removed from it and considered synonyms (Pardiñas and Barbière 2018). In spite of these advances, Wiedomys remains an enigmatic genus, especially regarding its alpha taxonomy. From its original description in 1821 until 2005, Wiedomys was a monotypic genus represented by W. pyrrhorhinos (Wied in Schinz 1821). Based on molecular, cytogenetic, and morphological approaches, Gonçalves et al. (2005) described a second species, W. cerradensis, which they considered endemic to the Cerrado, as it was known only from its type locality in southwestern Bahia state. In turn, W. pyrrhorhinos was thought to occupy a broad area in northeastern Brazil, throughout the Caatinga and its transitional areas with the Atlantic Forest and Cerrado, from northern Minas Gerais state to Bahia, Sergipe, eastern Alagoas, and Pernambuco states (Bonvicino 2015). At the time, these species could also be distinguished by their respective karyotypes: W. pyrrhorhinos with 2n = 62, FN = 86, 90, 98 to 99, and 104 (Maia and Langguth 1987; Souza et al. 2011; Bezerra et al. 2014; Geise et al. 2017), and Wiedomys cerradensis with 2n = 60, FN = 88 (Gonçalves et al. 2005).
Recent records based on genetically analyzed specimens have considerably expanded the geographic range of W. cerradensis to Goiás and Tocantins states (Bezerra et al. 2013), in central Cerrado biome, northwards into the Cerrado of Maranhão state (Olímpio et al. 2016), and into the Caatinga in Ceará state (Bonvicino 2015). Recent treatises of rodents (Patton et al. 2015; Pardiñas 2017) already incorporated these proposed changes, indicating that the 2 Wiedomys species were distributed along the São Francisco River. Despite this progress, the geographic limits of the 2 species remain uncertain, particularly because the morphological and cytogenetic variation distinguishing the species has not been revised since the original description of W. cerradensis. Consequently, the identification of new samples of both species has relied almost exclusively on mitochondrial Cytochrome b (mt-Cytb) sequences, without further analyses of cytogenetic and detailed morphological variation. Additionally, the broad distribution of Wiedomys in northeastern Brazil offers an excellent opportunity to evaluate whether the São Francisco River would be coincident with the variation between or within species. According to the riverine barrier hypothesis, if the São Francisco River represents a primary barrier for Wiedomys lineages, divergence between species (or populations) would be spatially and temporally coincident with the formation of the current river course separating them (Moritz et al. 2000). Alternatively, if the current river course acts as a secondary barrier to lineages that diverged elsewhere or that dispersed after the establishment of the actual river course, there would be spatial but not temporal coincidence between the river course and multiple co-distributed species boundaries. Therefore, an integrative approach to assess diversity in the genus Wiedomys has the potential to shed light on both its taxonomy and biogeography throughout the Cerrado and Caatinga biomes.
In this study, we aim to provide an updated diagnosis of Wiedomys species by integrating phylogenetic, cytogenetic, and morphological analyses, and to discuss the implication of these results for the hypothesis that São Francisco River has operated historically as a vicariant barrier in the diversification of this genus.
Materials and methods
Samples
Morphological analyses were based on 282 specimens of the genus Wiedomys, housed at the following Brazilian mammal collections: Museu Nacional/Universidade Federal do Rio de Janeiro (MN/UFRJ), Rio de Janeiro-RJ; Museu de Ciências Naturais da Pontifícia Universidade Católica de Minas Gerais (MCN/PUC-Minas), Belo Horizonte-MG; Coleção de Mamíferos, Universidade de Brasília (UnB), Brasília-DF; and Museu de História Natural da Universidade Federal de Alagoas (MHN/UFAL), Maceió-AL (Appendix I). Molecular analyses were performed on sequenced samples from 50 specimens, from which 25 were karyotyped and 26 were morphologically examined (Appendix I; Fig. 1). The specimens examined comprised the entire extant distribution known for the genus (Fig. 1), including a specimen close to the type locality of W. pyrrhorhinos (Ribeirão da Ressaca, Piripá, Bahia state; locality 10 in Fig. 1) and the holotype of W. cerradensis.

Collection localities (see Table 1 for number identification) of specimens and OTUs used in morphological and/or genetic analyses of Wiedomys spanning the known distribution of the genus. OTU ellipses are colored according to their location at the left (green) and right (blue) sides of the São Francisco River (bold blue line).
OTUs of Wiedomys examined in this study for morphological, cytogenetic, and molecular phylogenetic analyses, including distribution of OTUs in relation to the São Francisco River (SF riverside), locality identifier (LI), sample size for morphometric analyses (n morph), karyotypes with diploid (2n) and fundamental (FN) numbers, and genetic data. Localities are mapped in Fig. 1.
OTU . | SF riverside . | LI . | Locality . | n morph . | Karyotype . | Genetic data . | |
---|---|---|---|---|---|---|---|
. | . | . | . | . | 2n . | FN . | . |
Berilo | Right | 1 | MG, Jenipapo de Minas | — | — | — | x |
Berilo | Right | 2 | MG, Leme do Prado (UHE Irapé) | 1 | — | — | — |
Berilo | Right | 3 | MG, Berilo | 16 | — | — | — |
Berilo | Right | 4 | MG, Araçuaí (Alto Caparaó) | 2 | — | — | — |
Berilo | Right | 5 | MG, Juramento (Fazenda Canoas) | 1 | — | — | x |
Berilo | Right | 6 | MG, José Gonçalves de Minas (UHE Irapé) | 7 | — | — | — |
Berilo | Right | 7 | MG, Grão Mogol (Fazenda do Matão) | 2 | — | — | — |
Berilo | Right | 8 | MG, Porteirinha | 1 | — | — | — |
Berilo | Right | 9 | MG, Jaíba (Parque Florestal de Jaíba) | 5 | — | — | — |
Caetité | Right | 10 | BA, Piripá (Ribeirão da Ressaca) | 1 | — | — | — |
Caetité | Right | 11 | BA, Vitória da Conquista (Sítio Caititu) | 10 | — | — | — |
Caetité | Right | 12 | BA, Caetité (Maniaçu) | 2 | 62 | 90 | x |
Caetité | Right | 13 | BA, Jequié (Fazenda Ipoeira) | 6 | — | — | — |
Caetité | Right | 14 | BA, Jaguaquara (Fazenda Vazante) | 5 | — | — | — |
Caetité | Right | 15 | BA, Santo Inácio | — | — | — | x |
Morro do Chapéu | Right | 16 | BA, Palmeiras (Sítio Ananaz) | 1 | — | — | — |
Morro do Chapéu | Right | 17 | BA, Seabra (Várzea da Canabrava) | 19 | — | — | — |
Morro do Chapéu | Right | 18 | BA, Morro do Chapéu (Fazenda Salinas) | 2 | 62 | 104 | x |
Feira de Santana | Right | 19 | BA, Feira de Santana (Fazenda Três Riachos) | 19 | — | — | — |
Serrinha | Right | 20 | BA, Serrinha (Fazenda Cruzeiro) | 6 | — | — | — |
Canindé de São Francisco | Right | 21 | SE, Nossa Senhora da Glória | — | 62 | 104 | x |
Canindé de São Francisco | Right | 22 | SE, Monte Alegre de Sergipe | — | 62 | 104 | x |
Canindé de São Francisco | Right | 23 | SE, Canindé de São Francisco (Miramar) | 6 | — | — | x |
Canindé de São Francisco | Right | 24 | BA, Curaçá | — | 62 | 96 | x |
Piranhas | Left | 25 | AL, Piranhas | 3 | 62 | 86 | x |
Piranhas | Left | 26 | AL, Delmiro Gouveia | 1 | 62 | 86 | x |
Piranhas | Left | 27 | AL, Olho d’Água do Casado (Curralinho) | 2 | 62 | 86 | — |
Piranhas | Left | 28 | AL, Inhapi | 2 | — | — | x |
Santana do Ipanema | Left | 29 | AL, Santana do Ipanema (Fazenda Santa Cruz II) | 8 | — | — | — |
Quebrangulo | Left | 30 | AL, Quebrangulo (Fazenda Lagoa dos Bois) | 17 | — | — | — |
Quebrangulo | Left | 31 | AL, Palmeira dos Índios (Sítio Ribeira) | 1 | — | — | — |
Quebrangulo | Left | 32 | AL, Limoeiro de Anadia (Sítio Cadoz) | 1 | — | — | — |
Garanhuns | Left | 33 | PE, Garanhuns (Sítio Canhoto) | 37 | — | — | — |
Pesqueira | Left | 34 | PE, Buíque (Serra do Catimbau) | — | 62 | 86 | x |
Pesqueira | Left | 35 | PE, Pesqueira (Sítio São Marcos) | 10 | — | — | — |
Pesqueira | Left | 36 | PE, Belo Jardim (Sítio Catota) | 1 | — | — | — |
Pesqueira | Left | 37 | PE, São Bento do Una (Sítio Mimoso) | 4 | — | — | — |
Caruaru | Left | 38 | PE, Caruaru (Sítio Preguiça) | 24 | — | — | — |
Caruaru | Left | 39 | PE, Bezerros | — | — | — | x |
Caruaru | Left | 40 | PE, Sítio Alfredo | — | — | — | x |
Ceará | Left | 41 | PE, Triunfo (Sítio Espírito Santo) | 8 | — | — | — |
Ceará | Left | 42 | PE, Bodocó (Sítio Socorro) | 10 | — | — | — |
Ceará | Left | 43 | CE, Jardim (Jardim (C02)) | 1 | — | — | — |
Ceará | Left | 44 | CE, Crato (Sítio Piaba) | 1 | — | — | — |
Ceará | Left | 45 | CE, Missão Velha (Santa Cachoeira) | 4 | — | — | — |
Ceará | Left | 46 | CE, Campos Sales | 5 | — | — | — |
Ceará | Left | 47 | CE, Russas | — | — | — | x |
Ceará | Left | 48 | CE, Jaguaruana | — | — | — | x |
Ceará | Left | 49 | CE, Monte Alegre | 3 | |||
Ceará | Left | 50 | CE, Guaraciaba do Norte | 1 | |||
Ceará | Left | 51 | CE, São Benedito | 5 | |||
Piauí | Left | 52 | PI, São João do Piauí (E13) | 2 | — | — | — |
Piauí | Left | 53 | PI, Canto do Buriti | 2 | — | — | — |
Piauí | Left | 54 | PI, Eliseu Martins | 2 | — | — | — |
Piauí | Left | 55 | PI, Uruçuí-Una | — | — | — | x |
Maranhão | Left | 56 | MA, Mirador | 1 | — | — | x |
Jaborandi | Left | 57 | TO, Paranã (Fazenda São João) | 3 | — | — | x |
Jaborandi | Left | 58 | BA, Correntina | 2 | |||
Jaborandi | Left | 59 | BA, Barreiras | 2 | |||
Jaborandi | Left | 60 | GO, São Domingos (Fazenda Cruzeiro do Sul) | 1 | — | — | — |
Jaborandi | Left | 61 | BA, Correntina (Fazenda Jatobá) | — | — | — | x |
Jaborandi | Left | 62 | BA, Jaborandi | 5 | 60 | 88 | x |
Jaborandi | Left | 63 | MG, Formoso (Parque Nacional Grande Sertão Veredas) | 1 | — | — | — |
OTU . | SF riverside . | LI . | Locality . | n morph . | Karyotype . | Genetic data . | |
---|---|---|---|---|---|---|---|
. | . | . | . | . | 2n . | FN . | . |
Berilo | Right | 1 | MG, Jenipapo de Minas | — | — | — | x |
Berilo | Right | 2 | MG, Leme do Prado (UHE Irapé) | 1 | — | — | — |
Berilo | Right | 3 | MG, Berilo | 16 | — | — | — |
Berilo | Right | 4 | MG, Araçuaí (Alto Caparaó) | 2 | — | — | — |
Berilo | Right | 5 | MG, Juramento (Fazenda Canoas) | 1 | — | — | x |
Berilo | Right | 6 | MG, José Gonçalves de Minas (UHE Irapé) | 7 | — | — | — |
Berilo | Right | 7 | MG, Grão Mogol (Fazenda do Matão) | 2 | — | — | — |
Berilo | Right | 8 | MG, Porteirinha | 1 | — | — | — |
Berilo | Right | 9 | MG, Jaíba (Parque Florestal de Jaíba) | 5 | — | — | — |
Caetité | Right | 10 | BA, Piripá (Ribeirão da Ressaca) | 1 | — | — | — |
Caetité | Right | 11 | BA, Vitória da Conquista (Sítio Caititu) | 10 | — | — | — |
Caetité | Right | 12 | BA, Caetité (Maniaçu) | 2 | 62 | 90 | x |
Caetité | Right | 13 | BA, Jequié (Fazenda Ipoeira) | 6 | — | — | — |
Caetité | Right | 14 | BA, Jaguaquara (Fazenda Vazante) | 5 | — | — | — |
Caetité | Right | 15 | BA, Santo Inácio | — | — | — | x |
Morro do Chapéu | Right | 16 | BA, Palmeiras (Sítio Ananaz) | 1 | — | — | — |
Morro do Chapéu | Right | 17 | BA, Seabra (Várzea da Canabrava) | 19 | — | — | — |
Morro do Chapéu | Right | 18 | BA, Morro do Chapéu (Fazenda Salinas) | 2 | 62 | 104 | x |
Feira de Santana | Right | 19 | BA, Feira de Santana (Fazenda Três Riachos) | 19 | — | — | — |
Serrinha | Right | 20 | BA, Serrinha (Fazenda Cruzeiro) | 6 | — | — | — |
Canindé de São Francisco | Right | 21 | SE, Nossa Senhora da Glória | — | 62 | 104 | x |
Canindé de São Francisco | Right | 22 | SE, Monte Alegre de Sergipe | — | 62 | 104 | x |
Canindé de São Francisco | Right | 23 | SE, Canindé de São Francisco (Miramar) | 6 | — | — | x |
Canindé de São Francisco | Right | 24 | BA, Curaçá | — | 62 | 96 | x |
Piranhas | Left | 25 | AL, Piranhas | 3 | 62 | 86 | x |
Piranhas | Left | 26 | AL, Delmiro Gouveia | 1 | 62 | 86 | x |
Piranhas | Left | 27 | AL, Olho d’Água do Casado (Curralinho) | 2 | 62 | 86 | — |
Piranhas | Left | 28 | AL, Inhapi | 2 | — | — | x |
Santana do Ipanema | Left | 29 | AL, Santana do Ipanema (Fazenda Santa Cruz II) | 8 | — | — | — |
Quebrangulo | Left | 30 | AL, Quebrangulo (Fazenda Lagoa dos Bois) | 17 | — | — | — |
Quebrangulo | Left | 31 | AL, Palmeira dos Índios (Sítio Ribeira) | 1 | — | — | — |
Quebrangulo | Left | 32 | AL, Limoeiro de Anadia (Sítio Cadoz) | 1 | — | — | — |
Garanhuns | Left | 33 | PE, Garanhuns (Sítio Canhoto) | 37 | — | — | — |
Pesqueira | Left | 34 | PE, Buíque (Serra do Catimbau) | — | 62 | 86 | x |
Pesqueira | Left | 35 | PE, Pesqueira (Sítio São Marcos) | 10 | — | — | — |
Pesqueira | Left | 36 | PE, Belo Jardim (Sítio Catota) | 1 | — | — | — |
Pesqueira | Left | 37 | PE, São Bento do Una (Sítio Mimoso) | 4 | — | — | — |
Caruaru | Left | 38 | PE, Caruaru (Sítio Preguiça) | 24 | — | — | — |
Caruaru | Left | 39 | PE, Bezerros | — | — | — | x |
Caruaru | Left | 40 | PE, Sítio Alfredo | — | — | — | x |
Ceará | Left | 41 | PE, Triunfo (Sítio Espírito Santo) | 8 | — | — | — |
Ceará | Left | 42 | PE, Bodocó (Sítio Socorro) | 10 | — | — | — |
Ceará | Left | 43 | CE, Jardim (Jardim (C02)) | 1 | — | — | — |
Ceará | Left | 44 | CE, Crato (Sítio Piaba) | 1 | — | — | — |
Ceará | Left | 45 | CE, Missão Velha (Santa Cachoeira) | 4 | — | — | — |
Ceará | Left | 46 | CE, Campos Sales | 5 | — | — | — |
Ceará | Left | 47 | CE, Russas | — | — | — | x |
Ceará | Left | 48 | CE, Jaguaruana | — | — | — | x |
Ceará | Left | 49 | CE, Monte Alegre | 3 | |||
Ceará | Left | 50 | CE, Guaraciaba do Norte | 1 | |||
Ceará | Left | 51 | CE, São Benedito | 5 | |||
Piauí | Left | 52 | PI, São João do Piauí (E13) | 2 | — | — | — |
Piauí | Left | 53 | PI, Canto do Buriti | 2 | — | — | — |
Piauí | Left | 54 | PI, Eliseu Martins | 2 | — | — | — |
Piauí | Left | 55 | PI, Uruçuí-Una | — | — | — | x |
Maranhão | Left | 56 | MA, Mirador | 1 | — | — | x |
Jaborandi | Left | 57 | TO, Paranã (Fazenda São João) | 3 | — | — | x |
Jaborandi | Left | 58 | BA, Correntina | 2 | |||
Jaborandi | Left | 59 | BA, Barreiras | 2 | |||
Jaborandi | Left | 60 | GO, São Domingos (Fazenda Cruzeiro do Sul) | 1 | — | — | — |
Jaborandi | Left | 61 | BA, Correntina (Fazenda Jatobá) | — | — | — | x |
Jaborandi | Left | 62 | BA, Jaborandi | 5 | 60 | 88 | x |
Jaborandi | Left | 63 | MG, Formoso (Parque Nacional Grande Sertão Veredas) | 1 | — | — | — |
OTUs of Wiedomys examined in this study for morphological, cytogenetic, and molecular phylogenetic analyses, including distribution of OTUs in relation to the São Francisco River (SF riverside), locality identifier (LI), sample size for morphometric analyses (n morph), karyotypes with diploid (2n) and fundamental (FN) numbers, and genetic data. Localities are mapped in Fig. 1.
OTU . | SF riverside . | LI . | Locality . | n morph . | Karyotype . | Genetic data . | |
---|---|---|---|---|---|---|---|
. | . | . | . | . | 2n . | FN . | . |
Berilo | Right | 1 | MG, Jenipapo de Minas | — | — | — | x |
Berilo | Right | 2 | MG, Leme do Prado (UHE Irapé) | 1 | — | — | — |
Berilo | Right | 3 | MG, Berilo | 16 | — | — | — |
Berilo | Right | 4 | MG, Araçuaí (Alto Caparaó) | 2 | — | — | — |
Berilo | Right | 5 | MG, Juramento (Fazenda Canoas) | 1 | — | — | x |
Berilo | Right | 6 | MG, José Gonçalves de Minas (UHE Irapé) | 7 | — | — | — |
Berilo | Right | 7 | MG, Grão Mogol (Fazenda do Matão) | 2 | — | — | — |
Berilo | Right | 8 | MG, Porteirinha | 1 | — | — | — |
Berilo | Right | 9 | MG, Jaíba (Parque Florestal de Jaíba) | 5 | — | — | — |
Caetité | Right | 10 | BA, Piripá (Ribeirão da Ressaca) | 1 | — | — | — |
Caetité | Right | 11 | BA, Vitória da Conquista (Sítio Caititu) | 10 | — | — | — |
Caetité | Right | 12 | BA, Caetité (Maniaçu) | 2 | 62 | 90 | x |
Caetité | Right | 13 | BA, Jequié (Fazenda Ipoeira) | 6 | — | — | — |
Caetité | Right | 14 | BA, Jaguaquara (Fazenda Vazante) | 5 | — | — | — |
Caetité | Right | 15 | BA, Santo Inácio | — | — | — | x |
Morro do Chapéu | Right | 16 | BA, Palmeiras (Sítio Ananaz) | 1 | — | — | — |
Morro do Chapéu | Right | 17 | BA, Seabra (Várzea da Canabrava) | 19 | — | — | — |
Morro do Chapéu | Right | 18 | BA, Morro do Chapéu (Fazenda Salinas) | 2 | 62 | 104 | x |
Feira de Santana | Right | 19 | BA, Feira de Santana (Fazenda Três Riachos) | 19 | — | — | — |
Serrinha | Right | 20 | BA, Serrinha (Fazenda Cruzeiro) | 6 | — | — | — |
Canindé de São Francisco | Right | 21 | SE, Nossa Senhora da Glória | — | 62 | 104 | x |
Canindé de São Francisco | Right | 22 | SE, Monte Alegre de Sergipe | — | 62 | 104 | x |
Canindé de São Francisco | Right | 23 | SE, Canindé de São Francisco (Miramar) | 6 | — | — | x |
Canindé de São Francisco | Right | 24 | BA, Curaçá | — | 62 | 96 | x |
Piranhas | Left | 25 | AL, Piranhas | 3 | 62 | 86 | x |
Piranhas | Left | 26 | AL, Delmiro Gouveia | 1 | 62 | 86 | x |
Piranhas | Left | 27 | AL, Olho d’Água do Casado (Curralinho) | 2 | 62 | 86 | — |
Piranhas | Left | 28 | AL, Inhapi | 2 | — | — | x |
Santana do Ipanema | Left | 29 | AL, Santana do Ipanema (Fazenda Santa Cruz II) | 8 | — | — | — |
Quebrangulo | Left | 30 | AL, Quebrangulo (Fazenda Lagoa dos Bois) | 17 | — | — | — |
Quebrangulo | Left | 31 | AL, Palmeira dos Índios (Sítio Ribeira) | 1 | — | — | — |
Quebrangulo | Left | 32 | AL, Limoeiro de Anadia (Sítio Cadoz) | 1 | — | — | — |
Garanhuns | Left | 33 | PE, Garanhuns (Sítio Canhoto) | 37 | — | — | — |
Pesqueira | Left | 34 | PE, Buíque (Serra do Catimbau) | — | 62 | 86 | x |
Pesqueira | Left | 35 | PE, Pesqueira (Sítio São Marcos) | 10 | — | — | — |
Pesqueira | Left | 36 | PE, Belo Jardim (Sítio Catota) | 1 | — | — | — |
Pesqueira | Left | 37 | PE, São Bento do Una (Sítio Mimoso) | 4 | — | — | — |
Caruaru | Left | 38 | PE, Caruaru (Sítio Preguiça) | 24 | — | — | — |
Caruaru | Left | 39 | PE, Bezerros | — | — | — | x |
Caruaru | Left | 40 | PE, Sítio Alfredo | — | — | — | x |
Ceará | Left | 41 | PE, Triunfo (Sítio Espírito Santo) | 8 | — | — | — |
Ceará | Left | 42 | PE, Bodocó (Sítio Socorro) | 10 | — | — | — |
Ceará | Left | 43 | CE, Jardim (Jardim (C02)) | 1 | — | — | — |
Ceará | Left | 44 | CE, Crato (Sítio Piaba) | 1 | — | — | — |
Ceará | Left | 45 | CE, Missão Velha (Santa Cachoeira) | 4 | — | — | — |
Ceará | Left | 46 | CE, Campos Sales | 5 | — | — | — |
Ceará | Left | 47 | CE, Russas | — | — | — | x |
Ceará | Left | 48 | CE, Jaguaruana | — | — | — | x |
Ceará | Left | 49 | CE, Monte Alegre | 3 | |||
Ceará | Left | 50 | CE, Guaraciaba do Norte | 1 | |||
Ceará | Left | 51 | CE, São Benedito | 5 | |||
Piauí | Left | 52 | PI, São João do Piauí (E13) | 2 | — | — | — |
Piauí | Left | 53 | PI, Canto do Buriti | 2 | — | — | — |
Piauí | Left | 54 | PI, Eliseu Martins | 2 | — | — | — |
Piauí | Left | 55 | PI, Uruçuí-Una | — | — | — | x |
Maranhão | Left | 56 | MA, Mirador | 1 | — | — | x |
Jaborandi | Left | 57 | TO, Paranã (Fazenda São João) | 3 | — | — | x |
Jaborandi | Left | 58 | BA, Correntina | 2 | |||
Jaborandi | Left | 59 | BA, Barreiras | 2 | |||
Jaborandi | Left | 60 | GO, São Domingos (Fazenda Cruzeiro do Sul) | 1 | — | — | — |
Jaborandi | Left | 61 | BA, Correntina (Fazenda Jatobá) | — | — | — | x |
Jaborandi | Left | 62 | BA, Jaborandi | 5 | 60 | 88 | x |
Jaborandi | Left | 63 | MG, Formoso (Parque Nacional Grande Sertão Veredas) | 1 | — | — | — |
OTU . | SF riverside . | LI . | Locality . | n morph . | Karyotype . | Genetic data . | |
---|---|---|---|---|---|---|---|
. | . | . | . | . | 2n . | FN . | . |
Berilo | Right | 1 | MG, Jenipapo de Minas | — | — | — | x |
Berilo | Right | 2 | MG, Leme do Prado (UHE Irapé) | 1 | — | — | — |
Berilo | Right | 3 | MG, Berilo | 16 | — | — | — |
Berilo | Right | 4 | MG, Araçuaí (Alto Caparaó) | 2 | — | — | — |
Berilo | Right | 5 | MG, Juramento (Fazenda Canoas) | 1 | — | — | x |
Berilo | Right | 6 | MG, José Gonçalves de Minas (UHE Irapé) | 7 | — | — | — |
Berilo | Right | 7 | MG, Grão Mogol (Fazenda do Matão) | 2 | — | — | — |
Berilo | Right | 8 | MG, Porteirinha | 1 | — | — | — |
Berilo | Right | 9 | MG, Jaíba (Parque Florestal de Jaíba) | 5 | — | — | — |
Caetité | Right | 10 | BA, Piripá (Ribeirão da Ressaca) | 1 | — | — | — |
Caetité | Right | 11 | BA, Vitória da Conquista (Sítio Caititu) | 10 | — | — | — |
Caetité | Right | 12 | BA, Caetité (Maniaçu) | 2 | 62 | 90 | x |
Caetité | Right | 13 | BA, Jequié (Fazenda Ipoeira) | 6 | — | — | — |
Caetité | Right | 14 | BA, Jaguaquara (Fazenda Vazante) | 5 | — | — | — |
Caetité | Right | 15 | BA, Santo Inácio | — | — | — | x |
Morro do Chapéu | Right | 16 | BA, Palmeiras (Sítio Ananaz) | 1 | — | — | — |
Morro do Chapéu | Right | 17 | BA, Seabra (Várzea da Canabrava) | 19 | — | — | — |
Morro do Chapéu | Right | 18 | BA, Morro do Chapéu (Fazenda Salinas) | 2 | 62 | 104 | x |
Feira de Santana | Right | 19 | BA, Feira de Santana (Fazenda Três Riachos) | 19 | — | — | — |
Serrinha | Right | 20 | BA, Serrinha (Fazenda Cruzeiro) | 6 | — | — | — |
Canindé de São Francisco | Right | 21 | SE, Nossa Senhora da Glória | — | 62 | 104 | x |
Canindé de São Francisco | Right | 22 | SE, Monte Alegre de Sergipe | — | 62 | 104 | x |
Canindé de São Francisco | Right | 23 | SE, Canindé de São Francisco (Miramar) | 6 | — | — | x |
Canindé de São Francisco | Right | 24 | BA, Curaçá | — | 62 | 96 | x |
Piranhas | Left | 25 | AL, Piranhas | 3 | 62 | 86 | x |
Piranhas | Left | 26 | AL, Delmiro Gouveia | 1 | 62 | 86 | x |
Piranhas | Left | 27 | AL, Olho d’Água do Casado (Curralinho) | 2 | 62 | 86 | — |
Piranhas | Left | 28 | AL, Inhapi | 2 | — | — | x |
Santana do Ipanema | Left | 29 | AL, Santana do Ipanema (Fazenda Santa Cruz II) | 8 | — | — | — |
Quebrangulo | Left | 30 | AL, Quebrangulo (Fazenda Lagoa dos Bois) | 17 | — | — | — |
Quebrangulo | Left | 31 | AL, Palmeira dos Índios (Sítio Ribeira) | 1 | — | — | — |
Quebrangulo | Left | 32 | AL, Limoeiro de Anadia (Sítio Cadoz) | 1 | — | — | — |
Garanhuns | Left | 33 | PE, Garanhuns (Sítio Canhoto) | 37 | — | — | — |
Pesqueira | Left | 34 | PE, Buíque (Serra do Catimbau) | — | 62 | 86 | x |
Pesqueira | Left | 35 | PE, Pesqueira (Sítio São Marcos) | 10 | — | — | — |
Pesqueira | Left | 36 | PE, Belo Jardim (Sítio Catota) | 1 | — | — | — |
Pesqueira | Left | 37 | PE, São Bento do Una (Sítio Mimoso) | 4 | — | — | — |
Caruaru | Left | 38 | PE, Caruaru (Sítio Preguiça) | 24 | — | — | — |
Caruaru | Left | 39 | PE, Bezerros | — | — | — | x |
Caruaru | Left | 40 | PE, Sítio Alfredo | — | — | — | x |
Ceará | Left | 41 | PE, Triunfo (Sítio Espírito Santo) | 8 | — | — | — |
Ceará | Left | 42 | PE, Bodocó (Sítio Socorro) | 10 | — | — | — |
Ceará | Left | 43 | CE, Jardim (Jardim (C02)) | 1 | — | — | — |
Ceará | Left | 44 | CE, Crato (Sítio Piaba) | 1 | — | — | — |
Ceará | Left | 45 | CE, Missão Velha (Santa Cachoeira) | 4 | — | — | — |
Ceará | Left | 46 | CE, Campos Sales | 5 | — | — | — |
Ceará | Left | 47 | CE, Russas | — | — | — | x |
Ceará | Left | 48 | CE, Jaguaruana | — | — | — | x |
Ceará | Left | 49 | CE, Monte Alegre | 3 | |||
Ceará | Left | 50 | CE, Guaraciaba do Norte | 1 | |||
Ceará | Left | 51 | CE, São Benedito | 5 | |||
Piauí | Left | 52 | PI, São João do Piauí (E13) | 2 | — | — | — |
Piauí | Left | 53 | PI, Canto do Buriti | 2 | — | — | — |
Piauí | Left | 54 | PI, Eliseu Martins | 2 | — | — | — |
Piauí | Left | 55 | PI, Uruçuí-Una | — | — | — | x |
Maranhão | Left | 56 | MA, Mirador | 1 | — | — | x |
Jaborandi | Left | 57 | TO, Paranã (Fazenda São João) | 3 | — | — | x |
Jaborandi | Left | 58 | BA, Correntina | 2 | |||
Jaborandi | Left | 59 | BA, Barreiras | 2 | |||
Jaborandi | Left | 60 | GO, São Domingos (Fazenda Cruzeiro do Sul) | 1 | — | — | — |
Jaborandi | Left | 61 | BA, Correntina (Fazenda Jatobá) | — | — | — | x |
Jaborandi | Left | 62 | BA, Jaborandi | 5 | 60 | 88 | x |
Jaborandi | Left | 63 | MG, Formoso (Parque Nacional Grande Sertão Veredas) | 1 | — | — | — |
Research on live animals followed ASM guidelines (Sikes et al. 2016) and ethical approval was granted by CEUA/Instituto Oswaldo Cruz L-036/2018 and CEUA/Instituto Butantan nº 1260/14. Permits for the collection of specimens were issued by Instituto Chico Mendes de Conservação da Biodiversidade-ICMBio and SISBIO (ICMBIO-187/2010, SISBIO-13373-1, 11375-2, 24003-12) and by Instituto Brasileiro do Meio Ambiente-IBAMA (CGFAP-189/2010).
DNA extraction, amplification, and sequencing
DNA was isolated from liver or muscle using Chelex (Walsh et al. 1991). Gene nomenclature followed Mouse Genome Database (Blake et al. 2021). Partial and complete mt-Cytb segments were amplified by polymerase chain reaction (PCR), using primers MVZ05 and MVZ16 (Irwin et al. 1991; Smith and Patton 1993) and Cytb-REV (Casado et al. 2010), respectively. We sequenced 2 nuclear loci, exon 1 of retinoid-binding protein (IRBP) using primers A1 and F (Stanhope et al. 1992) and intron 7 of the beta-fibrinogen (i7Fgb), using primers Β17-mammL and Βfib-mammaU (Matocq et al. 2007). PCR was conducted in a thermal cycler (Eppendorf Mastercycler ep Gradient, Model 5341) by using cocktails with a final volume of 18 μL containing 0.2 units of Platinum Taq DNA Polymerase (Invitrogen), 30 ng of DNA, 25 pmol of each primer, 0.2 mM of dNTP, and 2.52 μL of reaction buffer (50 mM KCl, 2.5 mM MgCl2, and 10 mM Tris–HCl; pH 8.8), following the thermal profile described by Suárez-Villota et al. (2018). PCR products were visualized using 1% agarose gel in TAE buffer, and the purification was carried out with ExoSAP-IT (Code number US78200, GE Healthcare).
Cycle sequencing was performed with BigDye (Applied Biosystems) in an ABI PRISM 3100 Genetic Analyzer (Applied Biosystems). Electropherograms were inspected and aligned with Geneious 7.1.7 (GeneMatters Corp; Kearse et al. 2012) using the MUSCLE algorithm implemented in the same software (Edgar 2004). Sequences were submitted to a comparative similarity search on BLAST before the alignment. All sequences generated by us were submitted to GenBank. In addition to sequences generated in this work, we included 61 sequences of mt-Cytb, IRBP, and i7Fgb downloaded from GenBank (Supplementary Data SD1). These encompassed 4 specimens of W. cerradensis (including the holotype), 4 specimens of W. pyrrhorhinos, and the remaining sequences belong to outgroup species composed of Wilfredomys oenax, Juliomys pictipes, and Phaenomys ferrugineus (as part of the Wiedomyini tribe); Abrothrix longipilis and Geoxus valdivianus (Abrotrichini tribe, sister to Wiedomyini); Delomys dorsalis, D. sublineatus, together with Calomys callosus, Phyllotis haggardi, and P. xanthopygus (representing the Delomys + Phyllotini clade, sister to Wiedomyini–Abrotrichini clade); and Rheomys raptor, Sigmodon hispidus, and S. toltecus (representing the most distantly related genera within Sigmodontinae), following Gonçalves et al. (2020; Supplementary Data SD1).
Phylogenetic analyses, species tree, and molecular dating
We used the following sets of data: (i) mt-Cytb gene sequences (mt), since this was the most informative gene in terms of number of sampled specimens; and (ii) a multilocus data set using mt-Cytb, IRBP, and i7Fgb sequences (mt + nuc). Models of nucleotide substitution and partitioning schemes were evaluated in PartitionFinder 2 (Lanfear et al. 2016), using the Bayesian information criterion (BIC). The best partition scheme suggested was partitioning by gene and codon position, except for noncoding i7Fgb sequences, to which a single partition and HKY + G model were proposed. SYM + G, HKY + I, and HKY + I + G were the models selected for each mt-Cytb codon positions, respectively. For IRBP, HKY + I was selected for position 1, K80 for position 2, and K80 + I for position 3.
We inferred molecular phylogenies using maximum likelihood (ML) and Bayesian inference (BI). ML analyses were performed using IQTree Web server (Trifinopoulos et al. 2016). Statistical support for nodes was estimated by nonparametric bootstrapping (BS) (Felsenstein 1985), with 1,000 pseudoreplicates. BI was carried out in MrBayes 3.2.6 (Ronquist and Huelsenbeck 2003). Markov chains were started from a random tree and run for 1.0 × 107 generations with sampling every 1,000th generation. The stationary phase was checked using Tracer 1.6 (Rambaut et al. 2014). Sample points prior to the plateau phase were discarded as burn-in, and the remaining trees were combined to find the maximum a posteriori estimated probability of the phylogeny. Branch supports were estimated with Bayesian posterior probabilities (PP). Two simultaneous analyses were performed to ensure convergence on topologies. To evaluate genetic and geographic population structure we reconstructed a Median-Joining (MJ) network (Bandelt et al. 1999) of mt-Cytb haplotypes using NETWORK10 (http://www.fluxus-engineering.com). This analysis was based on variable sites and excluded sites containing missing data.
The evolutionary distance between pairs of sequences was estimated with MEGA 11 (Tamura et al. 2021), using the Tamura–Nei model with gamma rate among sites for mt-Cytb gene and Kimura 2-parameter model for nuclear sequences data sets (IRBP and i7Fgb). The goodness of fit of these models to data sets was measured also in MEGA 11 by the BIC and corrected by Akaike information criterion. For mt-Cytb, we analyzed a total of 51 sequences (32 from W. cerradensis and 19 from W. pyrrhorhinos). For nuclear data sets, 38 sequences of i7Fgb (24 from W. cerradensis and 14 from W. pyrrhorhinos) and 25 sequences of IRBP (18 from W. cerradensis and 7 from W. pyrrhorhinos) were analyzed.
We inferred the species tree by using multispecies coalescent analyses and molecular dating in BEAST 2.7.3 (Drummond and Rambaut 2007; Suchard and Rambaut 2009). Gene trees for the partitioned mt + nuc data set were simultaneously estimated and reconciled onto a species tree using the Bayesian multispecies coalescent (MSC) method (Heled and Drummond 2010). The mt + nuc data set used in the MSC included all Wiedomys samples (44 terminals) with the 3 loci sequenced and 3 samples for each genus used as outgroup (Supplementary Data SD1). We used a Yule model as the prior to genes and species trees and the multispecies coalescent population size was set to “Constant population.” The MCMC was run for 400 million generations, sampling parameters values, gene trees, and species trees every 10,000 generations. We checked the convergence through effective sample sizes (ESS > 200) of estimated parameters on TRACER 1.6 and by comparing the topologies across multiple independent runs. Consensus for species trees and gene trees were annotated from MCMC samples using TreeAnnotator 2.4.2, with the first 10% of samples discarded as burn-in.
In the same analyses, the crown age for the genus Wiedomys was estimated. Ages of 6 clades were constrained as calibration points with time units in millions of years ago (Ma) based on Gonçalves et al. (2020), Ronez et al. (2021), Parada et al. (2021), and Salazar-Bravo et al. (2023): (i) Sigmodontalia (offset: 6.79); (ii) Sigmodon (offset: 2.5); (iii) Phyllotini (offset: 4.3 Ma); (iv) Abrotrichini (offset: 1.7 Ma); (v) Wiedomyini–Abrotrichini (offset: 5.19 Ma); and (vi) Wiedomyini (offset: 0.85 Ma). For calibration points, we used log-normal distribution priors (Ho and Phillips 2009) with offsets adjusted to accommodate fossil dates (i.e., clade minimum age) within the first fifth percentile of a log-normal distribution with mean 0.01 and standard deviation 1.0.
Chromosome analyses
Chromosome suspensions were obtained from different sampling collections and using 2 methods, respectively: in vivo, from spleen and bone marrow following Ford and Hamerton (1956); and in vitro, with short-term bone marrow cultures incubated for 2 h (around 37 °C) in 15-mL polypropylene tubes containing sterile medium (80% RPMI, 20% fetal calf serum, 5 μg of ethidium bromide, and 10-6 M colchicine). Conventional Giemsa staining and CBG-banding (when possible) were performed according to Sumner (1972). Metaphases were captured with visible light on an Axioskop 40 microscope (Zeiss) using AxioVision software.
Morphological analyses
Specimens were classified into 7 age classes based on molar tooth eruption and wear according to criteria defined in Sobral and Oliveira (2014). Morphometric analyses included only skulls of adult specimens (age classes 5 to 7). Twenty craniodental and mandibular measurements (Supplementary Data SD2) were taken with the aid of a digital caliper nearest to 0.01 mm of precision. Adult specimens with less than 4 missing measurements were used for morphometric analyses, which resulted in a matrix of 165 specimens. To make this matrix complete, we inferred values for up to 4 missing measurements per specimen (20% of the total) using the Expectation-Maximization Bootstrapping routine in the R v. 4.2.1 (R Core Team 2022) package “Amelia II” (Honaker et al. 2011).
As most localities had less than 5 specimens, geographic samples were pooled into 16 operational taxonomic units (OTUs) based on their geographical proximity and absence of geographical barriers among collecting localities (Table 1). Among these OTUs, 8 comprised specimens included in cytogenetic and molecular analyses, 1 included topotypes of W. pyrrhorhinos (OTU Caetité—Bahia state, right riverside), and 1 included the holotype of W. cerradensis (OTU Jaborandi—Bahia state, left riverside). This correspondence among data types allowed us to assign OTUs inferred by morphological groupings to genetic lineages, karyotypes, and species (Table 1).
To estimate patterns of craniometric discrimination among Wiedomys OTUs, a canonical variate analysis (CVA) was carried out based on the 20 log-transformed cranial measurements (Supplementary Data SD2). The specimen OTUs were used as prior classification in CVA so that we could test whether patterns of morphometric discrimination were congruent with the genetic lineages revealed by molecular analysis. After species names were assigned to morphological groups revealed by the CVA, we assessed the amount of a posteriori correct classifications between species based on 1,000 jack-knife pseudoreplicates of the discrimination functions estimated in the OTUs CVA.
We also evaluated qualitative variation among and within OTUs in the following external and cranial characters: size and distribution of chromogenic patches of hairs on the head; alisphenoid strut presence; mesopterygoid fossa terminal edge shape; frontal–parietal–squamosal suture shape; nasal morphology; and molar characters. We used the anatomical terminology of Carleton and Musser (1989), Voss (1991), Weksler (2006), and Barbière et al. (2019) for these characters.
Results
Phylogenetic relationships and divergence time estimation
The topology based on the mt + nuc data set using the multispecies coalescent method recovered Wiedomys as monophyletic and Wilfredomys as the sister genus with both relationships highly supported (PP = 1.0; Fig. 2A). This topology was supported by all gene trees derived from different partitions of the mt + nuc data set, although mt-Cytb third positions and IRBP first and second positions yielded lower support values (PP < 0.85) for the monophyly of Wiedomys (Supplementary Data SD3). The relationship between Wiedomys and Wilfredomys inferred exclusively from the mt data set using the ML and BI methods (Supplementary Data SD4) differed from that inferred from the mt + nuc data set. The mt topology recovered 3 highly supported clades (BS—100%/PP = 1), but recovered Wiedomys as paraphyletic, with W. pyrrhorhinos as the sister to W. oenax (BS = 73%/PP = 0.88; Supplementary Data SD4).

(A) Multispecies coalescent tree analysis of Wiedomys using mt-Cytb, IRBP, and i7Fgb sequences. Circles indicate posterior probability (above) and bootstrap (below) values: black > 0.95% and 90%, gray 75% to 90%, and white < 0.95% and 75%. * represents W. cerradensis type series. (B) Divergence time estimates of Wiedomys species based on multispecies coalescent analysis of the multilocus data set (mt-Cytb, IRBP, i7Fgb). Numbers below branches are mean height and maximum and minimum height. Bars on nodes indicate 95% credibility intervals of date estimates.
In all analyses of mt and mt + nuc data sets, the W. pyrrhorhinos lineage was recovered grouping samples from the right bank of the São Francisco River—distributed throughout Bahia, Sergipe, and Minas Gerais states—and the W. cerradensis lineage included samples from the left bank of the São Francisco River, distributed throughout localities of Cerrado and Caatinga of Alagoas, Bahia, Ceará, Goiás, Maranhão, Pernambuco, Piauí, and Tocantins states (Figs. 1 and 2A; Supplementary Data SD4). The mean genetic distance of mt-Cytb between W. pyrrhorhinos and W. cerradensis was 17% (ranging from 13% to 19%), within W. pyrrhorhinos 0.7% (range: 0.0% to 1.5%), and within W. cerradensis 1% (range: 0.0% to 2.5%). The mean genetic distance obtained using nuclear sequences (IRBP + i7Fgb) between W. pyrrhorhinos and W. cerradensis was 1% (ranging from 0.0% to 3.0%), within W. pyrrhorhinos 0.4% (range: 0.0% to 1.4%), and within W. cerradensis 0.5% (range: 0.0% to 2.9%). The genus Wiedomys showed high haplotype diversity (Hd = 0.99). The MJ network (Fig. 3) of 46 sequences of at least 771 bp was highly concordant with the pattern shown in the phylogenetic analyses, recovering 2 haplogroups separated by 84 substitutions: the W. pyrrhorhinos haplogroup with 15 haplotypes (n = 19 sequences); and the W. cerradensis haplogroup with 24 haplotypes (n = 27). The network did not show any clear structure among specimens with the same haplogroup.

Median-joining network of Wiedomys specimen haplotypes based on mt-Cytb (n = 165). Circle size corresponds to the number of individuals with a given haplotype. Diploid and fundamental numbers (when available) are shown below the haplotype indication, as well as the Brazilian state abbreviation (see Table 1) from where the individuals were collected. Black circles represent median vectors. Numbers and lines in connecting branches denote more than 2 nucleotide substitutions; straight lines indicate one nucleotide substitution.
Molecular dating showed that the divergence between lineages in the Wiedomys–Wilfredomys clade occurred during the Late Quaternary. Wilfredomys and Wiedomys diverged at approximately 0.38 Ma (Highest Posterior Density (HPD) 95% interval = 0.09 to 0.8 Ma), while W. pyrrhorhinos and W. cerradensis split approximately at 0.15 Ma (HPD 95% interval = 0.02 to 0.34 Ma; Fig. 2B).
Cytogenetic variation
The karyotypes of W. pyrrhorhinos from Curaçá (Bahia state) and W. cerradensis from Jaguaruana (Ceará state) are described for the first time. Wiedomys pyrrhorhinos had a karyotype of 2n = 62, FN = 96, with the autosome complement composed of 18 biarmed pairs and 12 acrocentric pairs; the X chromosome is a large submetacentric and the Y is a small acrocentric (Fig. 4A).

New karyotypes described for Wiedomys. (A) Wiedomys pyrrhorhinos (CIT959), male, from Curaçá (Bahia State) with 2n = 62, FN = 96; (B) W. cerradensis (LBCE5255), female, from Jaguaruana (Ceará s tate) with 2n = 62, FN = 88.
Wiedomys cerradensis had a karyotype of 2n = 62, FN = 86 for samples from Piranhas and Delmiro Gouveia (Alagoas state), and 2n = 62, FN = 88 for samples from Jaguaruana (Ceará state). Autosome complement is composed of 13 biarmed pairs and 17 acrocentric pairs in samples from Alagoas (not shown) and 14 biarmed pairs and 16 acrocentric pairs in samples from Ceará. The 2 karyotypes showed a large acrocentric pair, the largest chromosome pair of the complement; the X is a large acrocentric (Fig. 4B) and the Y is a small acrocentric (not shown).
Morphological variation
The first 3 canonical variates (CVA), based on 20 craniometric measurements, summarized 60.15% of total variation among the 16 morphological OTUs (Fig. 5). CV1 predominantly represented a gradient of cranial size variation among samples, as all characters were positively correlated with this axis, while CV2 and CV3 represented different trends of cranial shape variation. The major trend of discrimination between OTUs was evidenced along CV1, mirroring the geographic distribution of samples between opposite sides of the São Francisco River. In general, OTUs on the left side of the river could be discriminated from OTUs on the right side by their relatively smaller cranial size. The sample from Piauí state illustrates a single exception to this trend as it presented the largest crania among the left-side OTUs, overlapping its 95% confidence ellipses more extensively with right-side OTUs such as samples from Feira de Santana (Bahia state) and Canindé de São Francisco (Sergipe state). However, discrimination between left-side and right-side OTUs was consistent in all other cases, even when left-side and right-side OTUs were geographically close, such as the Piranhas (Alagoas State) and Canindé de São Francisco OTUs (Fig. 1).

Craniometric discrimination among Wiedomys OTUs provided by CVA: (A, C) centroids and 95% confidence ellipses of OTUs along the first 3 canonical variates; and (B, D) respective vector correlations among characters and canonical variates.
Jaborandi is the type locality, since it includes the holotype of W. cerradensis, and this OTU was found to be on the left side of the São Francisco River, while Caetité, which includes a topotype of W. pyrrhorhinos and also presents the largest crania of all samples, is an OTU distributed on the right side of the São Francisco River. Therefore, OTUs from the left riverside can be referred to W. cerradensis, whereas OTUs from the right riverside are referred to W. pyrrhorhinos, consistent with the taxonomic assignment of left-side and right-side lineages delineated in the molecular phylogenetic analyses (Fig. 2A). When OTUs are assigned to these 2 species, the discriminant functions correctly classify 71.4% of the specimens of W. pyrrhorhinos and 82% of the specimens of W. cerradensis.
We also observed consistent variation between species in the size of the ring of orangish hairs around the eyes (periocular ring) and in its connection to the patch of orangish hairs in the muzzle (Fig. 6; Table 2). In all skins of W. cerradensis analyzed (n = 65), specimens present a wide and conspicuous periocular ring, which in most of them (84%) extends along the infraorbital region and reaches the patch of orangish hairs in the muzzle (Fig. 6A). The wide periocular ring gives the appearance that these 2 chromogenic patches are contiguous. In contrast, most specimens (n = 50) of W. pyrrhorhinos present a narrower periocular ring (90%), sometimes incomplete or inconspicuous (10%), which is always separated from the muzzle patch by a strip of grizzled hairs along the infraorbital region. These grizzled hairs are of similar color to those from the frontal and/or cheek regions of the head, giving the appearance that the periocular ring and the orangish patches on the muzzle are completely separated or discontinuous. In some W. cerradensis specimens (16% examined here), the 2 chromogenic patches are discontinuous, approaching the most common condition seen in W. pyrrhorhinos. But no W. pyrrhorhinos specimen analyzed exhibited the most common condition seen in W. cerradensis (broad periocular ring connected to the muzzle patch).
Frequencies of the orangish periocular ring character-states in population samples and species of Wiedomys (see Fig. 6A–C). Average frequencies for the 2 species are in bold.
Species/OTU . | n . | Periocular ring . | ||
---|---|---|---|---|
Broad and contiguous to the muzzle patch . | Narrow and separated from muzzle patch . | Incomplete and separated from muzzle patch . | ||
Wiedomys cerradensis | ||||
Caruaru | 2 | 0.50 | 0.50 | 0.00 |
Ceará | 28 | 0.83 | 0.17 | 0.00 |
Garanhuns | 19 | 0.79 | 0.21 | 0.00 |
Jaborandi | 6 | 0.67 | 0.33 | 0.00 |
Maranhão | 1 | 1.00 | 0.00 | 0.00 |
Pesqueira | 14 | 0.93 | 0.07 | 0.00 |
Piauí | 4 | 0.75 | 0.25 | 0.00 |
Piranhas | 1 | 1.00 | 0.00 | 0.00 |
Quebrangulo | 13 | 1.00 | 0.00 | 0.00 |
Santana do Ipanema | 5 | 0.80 | 0.20 | 0.00 |
Total | 65 | 0.84 | 0.16 | 0.00 |
Wiedomys pyrrhorhinos | ||||
Berilo | 10 | 0.00 | 0.90 | 0.10 |
Caetité | 13 | 0.00 | 0.92 | 0.08 |
Canindé de São Francisco | 1 | 0.00 | 1.00 | 0.00 |
Feira de Santana | 17 | 0.00 | 0.82 | 0.18 |
Morro do Chapéu | 4 | 0.00 | 1.00 | 0.00 |
Serrinha | 5 | 0.00 | 1.00 | 0.00 |
Total | 50 | 0.00 | 0.91 | 0.09 |
Species/OTU . | n . | Periocular ring . | ||
---|---|---|---|---|
Broad and contiguous to the muzzle patch . | Narrow and separated from muzzle patch . | Incomplete and separated from muzzle patch . | ||
Wiedomys cerradensis | ||||
Caruaru | 2 | 0.50 | 0.50 | 0.00 |
Ceará | 28 | 0.83 | 0.17 | 0.00 |
Garanhuns | 19 | 0.79 | 0.21 | 0.00 |
Jaborandi | 6 | 0.67 | 0.33 | 0.00 |
Maranhão | 1 | 1.00 | 0.00 | 0.00 |
Pesqueira | 14 | 0.93 | 0.07 | 0.00 |
Piauí | 4 | 0.75 | 0.25 | 0.00 |
Piranhas | 1 | 1.00 | 0.00 | 0.00 |
Quebrangulo | 13 | 1.00 | 0.00 | 0.00 |
Santana do Ipanema | 5 | 0.80 | 0.20 | 0.00 |
Total | 65 | 0.84 | 0.16 | 0.00 |
Wiedomys pyrrhorhinos | ||||
Berilo | 10 | 0.00 | 0.90 | 0.10 |
Caetité | 13 | 0.00 | 0.92 | 0.08 |
Canindé de São Francisco | 1 | 0.00 | 1.00 | 0.00 |
Feira de Santana | 17 | 0.00 | 0.82 | 0.18 |
Morro do Chapéu | 4 | 0.00 | 1.00 | 0.00 |
Serrinha | 5 | 0.00 | 1.00 | 0.00 |
Total | 50 | 0.00 | 0.91 | 0.09 |
Frequencies of the orangish periocular ring character-states in population samples and species of Wiedomys (see Fig. 6A–C). Average frequencies for the 2 species are in bold.
Species/OTU . | n . | Periocular ring . | ||
---|---|---|---|---|
Broad and contiguous to the muzzle patch . | Narrow and separated from muzzle patch . | Incomplete and separated from muzzle patch . | ||
Wiedomys cerradensis | ||||
Caruaru | 2 | 0.50 | 0.50 | 0.00 |
Ceará | 28 | 0.83 | 0.17 | 0.00 |
Garanhuns | 19 | 0.79 | 0.21 | 0.00 |
Jaborandi | 6 | 0.67 | 0.33 | 0.00 |
Maranhão | 1 | 1.00 | 0.00 | 0.00 |
Pesqueira | 14 | 0.93 | 0.07 | 0.00 |
Piauí | 4 | 0.75 | 0.25 | 0.00 |
Piranhas | 1 | 1.00 | 0.00 | 0.00 |
Quebrangulo | 13 | 1.00 | 0.00 | 0.00 |
Santana do Ipanema | 5 | 0.80 | 0.20 | 0.00 |
Total | 65 | 0.84 | 0.16 | 0.00 |
Wiedomys pyrrhorhinos | ||||
Berilo | 10 | 0.00 | 0.90 | 0.10 |
Caetité | 13 | 0.00 | 0.92 | 0.08 |
Canindé de São Francisco | 1 | 0.00 | 1.00 | 0.00 |
Feira de Santana | 17 | 0.00 | 0.82 | 0.18 |
Morro do Chapéu | 4 | 0.00 | 1.00 | 0.00 |
Serrinha | 5 | 0.00 | 1.00 | 0.00 |
Total | 50 | 0.00 | 0.91 | 0.09 |
Species/OTU . | n . | Periocular ring . | ||
---|---|---|---|---|
Broad and contiguous to the muzzle patch . | Narrow and separated from muzzle patch . | Incomplete and separated from muzzle patch . | ||
Wiedomys cerradensis | ||||
Caruaru | 2 | 0.50 | 0.50 | 0.00 |
Ceará | 28 | 0.83 | 0.17 | 0.00 |
Garanhuns | 19 | 0.79 | 0.21 | 0.00 |
Jaborandi | 6 | 0.67 | 0.33 | 0.00 |
Maranhão | 1 | 1.00 | 0.00 | 0.00 |
Pesqueira | 14 | 0.93 | 0.07 | 0.00 |
Piauí | 4 | 0.75 | 0.25 | 0.00 |
Piranhas | 1 | 1.00 | 0.00 | 0.00 |
Quebrangulo | 13 | 1.00 | 0.00 | 0.00 |
Santana do Ipanema | 5 | 0.80 | 0.20 | 0.00 |
Total | 65 | 0.84 | 0.16 | 0.00 |
Wiedomys pyrrhorhinos | ||||
Berilo | 10 | 0.00 | 0.90 | 0.10 |
Caetité | 13 | 0.00 | 0.92 | 0.08 |
Canindé de São Francisco | 1 | 0.00 | 1.00 | 0.00 |
Feira de Santana | 17 | 0.00 | 0.82 | 0.18 |
Morro do Chapéu | 4 | 0.00 | 1.00 | 0.00 |
Serrinha | 5 | 0.00 | 1.00 | 0.00 |
Total | 50 | 0.00 | 0.91 | 0.09 |

Variation in the size of periocular ring of orangish hairs and on its connection with the patch of orangish hairs in the muzzle of Wiedomys: (A) broad periocular ring contiguously connected to the muzzle patch (Wiedomys cerradensis, MN67022); (B) narrower periocular ring disconnected from the muzzle patch (W. cerradensis, MN18554); and (C) incomplete or inconspicuous periocular ring disconnected from the muzzle patch (Wiedomys pyrrhorhinos, MN18762).
Among qualitative cranial characters, nasal bone morphology was the most useful to differentiate W. cerradensis and W. pyrrhorhinos, showing no polymorphism within OTUs (Table 2). Wiedomys cerradensis present relatively short nasals, with their posterior margin terminating in level with the frontal–premaxillary sutures, while W. pyrrhorhinos present longer nasals, with their posterior margins extending beyond the frontal–premaxillary sutures (Fig. 7). The anterior outlines of nasals also vary between species. In W. cerradensis, the anterior margins of nasals taper continuously to the midline, producing a more pointed and shorter rostrum, while in W. cerradensis the nasal anterior margins are rounded, giving the rostrum a more blunt and stocky appearance (Figs. 7 and 8).

Dorsal views of the rostrum showing variation in the morphology of the posterior margin of nasals: (A) Wiedomys cerradensis (MUFAL249, Piranhas, Alagoas state) exhibiting a short nasal with its posterior margin terminating in level with the frontal–premaxillary suture, and (B) Wiedomys pyrrhorhinos (MUFAL265, Canindé de São Francisco, Sergipe state) showing a long nasal with the posterior margin extending beyond the frontal–premaxillary suture.

Dorsal, ventral, and lateral views of skulls and lateral view of mandibles of Wiedomys cerradensis (MUFAL250, Piranhas, Alagoas state) and W. pyrrhorhinos (MUFAL265, Canindé de São Francisco, Sergipe state).
All other cranial qualitative characters presented high levels of polymorphism and were not informative for discrimination between species (Table 3). These polymorphic characters include the occurrence of a bony alisphenoid strut, which was considered as diagnostic by Gonçalves et al. (2005) but exhibited variation within the OTUs examined here (Table 3). Dental characters also exhibited polymorphism within the 2 species, but when young adults of the same age category are compared, W. cerradensis most frequently exhibit a broader anteromedian style in the procingulum of M1 relative to W. pyrrhorhinos.
Frequencies of cranial character-states in population samples (n shown) and species of Wiedomys. Total frequencies for the 2 species are in bold.
Species/OTU . | n . | Nasals . | Alisphenoid strut . | Mesopterygoid fossa margin . | Frontoparietal suture . | |||||
---|---|---|---|---|---|---|---|---|---|---|
. | . | Short . | Long . | Absent . | Present . | Rounded . | Pointed . | Squared . | U . | V . |
W. cerradensis | ||||||||||
Caruaru | 23 | 1.00 | 0.00 | 1.00 | 0.00 | 0.46 | 0.00 | 0.54 | 0.26 | 0.74 |
Ceará | 18 | 1.00 | 0.00 | 0.19 | 0.81 | 0.13 | 0.07 | 0.80 | 0.06 | 0.94 |
Garanhuns | 18 | 1.00 | 0.00 | 0.89 | 0.11 | 0.82 | 0.00 | 0.18 | 0.00 | 1.00 |
Jaborandi | 8 | 1.00 | 0.00 | 0.22 | 0.78 | 1.00 | 0.00 | 0.00 | 0.11 | 0.89 |
Pesqueira | 9 | 1.00 | 0.00 | 0.42 | 0.58 | 0.78 | 0.00 | 0.22 | 0.00 | 1.00 |
Piauí | 4 | 1.00 | 0.00 | 0.33 | 0.67 | 0.67 | 0.00 | 0.33 | 0.00 | 1.00 |
Piranhas | 7 | 1.00 | 0.00 | 1.00 | 0.00 | 0.89 | 0.00 | 0.11 | 0.00 | 1.00 |
Quebrangulo | 11 | 1.00 | 0.00 | 0.37 | 0.63 | 0.63 | 0.00 | 0.37 | 0.15 | 0.85 |
Santana do Ipanema | 6 | 1.00 | 0.00 | 0.09 | 0.91 | 0.71 | 0.00 | 0.29 | 0.23 | 0.77 |
Total/mean | 104 | 1.00 | 0.00 | 0.50 | 0.50 | 0.68 | 0.01 | 0.32 | 0.09 | 0.91 |
W. pyrrhorhinos | ||||||||||
Berilo | 26 | 0.00 | 1.00 | 0.31 | 0.77 | 0.59 | 0.35 | 0.07 | 0.00 | 1.00 |
Caetité | 17 | 0.00 | 1.00 | 0.50 | 0.50 | 0.68 | 0.23 | 0.09 | 0.14 | 0.86 |
Canindé de São Francisco | 5 | 0.00 | 1.00 | 0.80 | 0.20 | 1.00 | 0.00 | 0.00 | 0.00 | 1.00 |
Feira de Santana | 17 | 0.00 | 1.00 | 0.71 | 0.29 | 1.00 | 0.00 | 0.00 | 0.35 | 0.65 |
Morro do Chapéu | 28 | 0.00 | 1.00 | 0.40 | 0.60 | 0.73 | 0.15 | 0.13 | 0.11 | 0.89 |
Serrinha | 6 | 0.00 | 1.00 | 0.29 | 0.71 | 0.86 | 0.00 | 0.14 | 0.29 | 0.71 |
Total/Mean | 99 | 0.00 | 1.00 | 0.50 | 0.51 | 0.81 | 0.12 | 0.07 | 0.15 | 0.85 |
Species/OTU . | n . | Nasals . | Alisphenoid strut . | Mesopterygoid fossa margin . | Frontoparietal suture . | |||||
---|---|---|---|---|---|---|---|---|---|---|
. | . | Short . | Long . | Absent . | Present . | Rounded . | Pointed . | Squared . | U . | V . |
W. cerradensis | ||||||||||
Caruaru | 23 | 1.00 | 0.00 | 1.00 | 0.00 | 0.46 | 0.00 | 0.54 | 0.26 | 0.74 |
Ceará | 18 | 1.00 | 0.00 | 0.19 | 0.81 | 0.13 | 0.07 | 0.80 | 0.06 | 0.94 |
Garanhuns | 18 | 1.00 | 0.00 | 0.89 | 0.11 | 0.82 | 0.00 | 0.18 | 0.00 | 1.00 |
Jaborandi | 8 | 1.00 | 0.00 | 0.22 | 0.78 | 1.00 | 0.00 | 0.00 | 0.11 | 0.89 |
Pesqueira | 9 | 1.00 | 0.00 | 0.42 | 0.58 | 0.78 | 0.00 | 0.22 | 0.00 | 1.00 |
Piauí | 4 | 1.00 | 0.00 | 0.33 | 0.67 | 0.67 | 0.00 | 0.33 | 0.00 | 1.00 |
Piranhas | 7 | 1.00 | 0.00 | 1.00 | 0.00 | 0.89 | 0.00 | 0.11 | 0.00 | 1.00 |
Quebrangulo | 11 | 1.00 | 0.00 | 0.37 | 0.63 | 0.63 | 0.00 | 0.37 | 0.15 | 0.85 |
Santana do Ipanema | 6 | 1.00 | 0.00 | 0.09 | 0.91 | 0.71 | 0.00 | 0.29 | 0.23 | 0.77 |
Total/mean | 104 | 1.00 | 0.00 | 0.50 | 0.50 | 0.68 | 0.01 | 0.32 | 0.09 | 0.91 |
W. pyrrhorhinos | ||||||||||
Berilo | 26 | 0.00 | 1.00 | 0.31 | 0.77 | 0.59 | 0.35 | 0.07 | 0.00 | 1.00 |
Caetité | 17 | 0.00 | 1.00 | 0.50 | 0.50 | 0.68 | 0.23 | 0.09 | 0.14 | 0.86 |
Canindé de São Francisco | 5 | 0.00 | 1.00 | 0.80 | 0.20 | 1.00 | 0.00 | 0.00 | 0.00 | 1.00 |
Feira de Santana | 17 | 0.00 | 1.00 | 0.71 | 0.29 | 1.00 | 0.00 | 0.00 | 0.35 | 0.65 |
Morro do Chapéu | 28 | 0.00 | 1.00 | 0.40 | 0.60 | 0.73 | 0.15 | 0.13 | 0.11 | 0.89 |
Serrinha | 6 | 0.00 | 1.00 | 0.29 | 0.71 | 0.86 | 0.00 | 0.14 | 0.29 | 0.71 |
Total/Mean | 99 | 0.00 | 1.00 | 0.50 | 0.51 | 0.81 | 0.12 | 0.07 | 0.15 | 0.85 |
Frequencies of cranial character-states in population samples (n shown) and species of Wiedomys. Total frequencies for the 2 species are in bold.
Species/OTU . | n . | Nasals . | Alisphenoid strut . | Mesopterygoid fossa margin . | Frontoparietal suture . | |||||
---|---|---|---|---|---|---|---|---|---|---|
. | . | Short . | Long . | Absent . | Present . | Rounded . | Pointed . | Squared . | U . | V . |
W. cerradensis | ||||||||||
Caruaru | 23 | 1.00 | 0.00 | 1.00 | 0.00 | 0.46 | 0.00 | 0.54 | 0.26 | 0.74 |
Ceará | 18 | 1.00 | 0.00 | 0.19 | 0.81 | 0.13 | 0.07 | 0.80 | 0.06 | 0.94 |
Garanhuns | 18 | 1.00 | 0.00 | 0.89 | 0.11 | 0.82 | 0.00 | 0.18 | 0.00 | 1.00 |
Jaborandi | 8 | 1.00 | 0.00 | 0.22 | 0.78 | 1.00 | 0.00 | 0.00 | 0.11 | 0.89 |
Pesqueira | 9 | 1.00 | 0.00 | 0.42 | 0.58 | 0.78 | 0.00 | 0.22 | 0.00 | 1.00 |
Piauí | 4 | 1.00 | 0.00 | 0.33 | 0.67 | 0.67 | 0.00 | 0.33 | 0.00 | 1.00 |
Piranhas | 7 | 1.00 | 0.00 | 1.00 | 0.00 | 0.89 | 0.00 | 0.11 | 0.00 | 1.00 |
Quebrangulo | 11 | 1.00 | 0.00 | 0.37 | 0.63 | 0.63 | 0.00 | 0.37 | 0.15 | 0.85 |
Santana do Ipanema | 6 | 1.00 | 0.00 | 0.09 | 0.91 | 0.71 | 0.00 | 0.29 | 0.23 | 0.77 |
Total/mean | 104 | 1.00 | 0.00 | 0.50 | 0.50 | 0.68 | 0.01 | 0.32 | 0.09 | 0.91 |
W. pyrrhorhinos | ||||||||||
Berilo | 26 | 0.00 | 1.00 | 0.31 | 0.77 | 0.59 | 0.35 | 0.07 | 0.00 | 1.00 |
Caetité | 17 | 0.00 | 1.00 | 0.50 | 0.50 | 0.68 | 0.23 | 0.09 | 0.14 | 0.86 |
Canindé de São Francisco | 5 | 0.00 | 1.00 | 0.80 | 0.20 | 1.00 | 0.00 | 0.00 | 0.00 | 1.00 |
Feira de Santana | 17 | 0.00 | 1.00 | 0.71 | 0.29 | 1.00 | 0.00 | 0.00 | 0.35 | 0.65 |
Morro do Chapéu | 28 | 0.00 | 1.00 | 0.40 | 0.60 | 0.73 | 0.15 | 0.13 | 0.11 | 0.89 |
Serrinha | 6 | 0.00 | 1.00 | 0.29 | 0.71 | 0.86 | 0.00 | 0.14 | 0.29 | 0.71 |
Total/Mean | 99 | 0.00 | 1.00 | 0.50 | 0.51 | 0.81 | 0.12 | 0.07 | 0.15 | 0.85 |
Species/OTU . | n . | Nasals . | Alisphenoid strut . | Mesopterygoid fossa margin . | Frontoparietal suture . | |||||
---|---|---|---|---|---|---|---|---|---|---|
. | . | Short . | Long . | Absent . | Present . | Rounded . | Pointed . | Squared . | U . | V . |
W. cerradensis | ||||||||||
Caruaru | 23 | 1.00 | 0.00 | 1.00 | 0.00 | 0.46 | 0.00 | 0.54 | 0.26 | 0.74 |
Ceará | 18 | 1.00 | 0.00 | 0.19 | 0.81 | 0.13 | 0.07 | 0.80 | 0.06 | 0.94 |
Garanhuns | 18 | 1.00 | 0.00 | 0.89 | 0.11 | 0.82 | 0.00 | 0.18 | 0.00 | 1.00 |
Jaborandi | 8 | 1.00 | 0.00 | 0.22 | 0.78 | 1.00 | 0.00 | 0.00 | 0.11 | 0.89 |
Pesqueira | 9 | 1.00 | 0.00 | 0.42 | 0.58 | 0.78 | 0.00 | 0.22 | 0.00 | 1.00 |
Piauí | 4 | 1.00 | 0.00 | 0.33 | 0.67 | 0.67 | 0.00 | 0.33 | 0.00 | 1.00 |
Piranhas | 7 | 1.00 | 0.00 | 1.00 | 0.00 | 0.89 | 0.00 | 0.11 | 0.00 | 1.00 |
Quebrangulo | 11 | 1.00 | 0.00 | 0.37 | 0.63 | 0.63 | 0.00 | 0.37 | 0.15 | 0.85 |
Santana do Ipanema | 6 | 1.00 | 0.00 | 0.09 | 0.91 | 0.71 | 0.00 | 0.29 | 0.23 | 0.77 |
Total/mean | 104 | 1.00 | 0.00 | 0.50 | 0.50 | 0.68 | 0.01 | 0.32 | 0.09 | 0.91 |
W. pyrrhorhinos | ||||||||||
Berilo | 26 | 0.00 | 1.00 | 0.31 | 0.77 | 0.59 | 0.35 | 0.07 | 0.00 | 1.00 |
Caetité | 17 | 0.00 | 1.00 | 0.50 | 0.50 | 0.68 | 0.23 | 0.09 | 0.14 | 0.86 |
Canindé de São Francisco | 5 | 0.00 | 1.00 | 0.80 | 0.20 | 1.00 | 0.00 | 0.00 | 0.00 | 1.00 |
Feira de Santana | 17 | 0.00 | 1.00 | 0.71 | 0.29 | 1.00 | 0.00 | 0.00 | 0.35 | 0.65 |
Morro do Chapéu | 28 | 0.00 | 1.00 | 0.40 | 0.60 | 0.73 | 0.15 | 0.13 | 0.11 | 0.89 |
Serrinha | 6 | 0.00 | 1.00 | 0.29 | 0.71 | 0.86 | 0.00 | 0.14 | 0.29 | 0.71 |
Total/Mean | 99 | 0.00 | 1.00 | 0.50 | 0.51 | 0.81 | 0.12 | 0.07 | 0.15 | 0.85 |
Discussion
Species boundaries and genus monophyly
Molecular and morphological analyses were congruent in supporting the presence of 2 species within living Wiedomys, corroborating the previous taxonomic assessment of the genus (Gonçalves et al. 2005). Phylogenetic analyses of mt-Cytb and the species tree approach evidenced a clear separation between the 2 species and did not reveal any geographic subdivision within either of them. This is evident in the low genetic distance among individuals within species compared to divergence among individuals between species. Morphological analyses also allowed both quantitative and qualitative discrimination of W. cerradensis and W. pyrrhorhinos. Previous analyses that relied on 2 adults and 1 young of W. cerradensis could not detect consistent morphometric discrimination between species despite including a large series of W. pyrrhorhinos (Gonçalves et al. 2005). Molecular and morphological results presented herein also revealed that samples from Alagoas and Pernambuco states treated by Gonçalves et al. (2005) as W. pyrrhorhinos are in fact W. cerradensis, posing considerable changes in the distributions of both species and in their cytogenetic variability. Current evidence suggests that W. cerradensis presents a much wider distribution than previous proposals, occurring throughout the Cerrado and Caatinga habitats of central and northeastern Brazil, respectively, while W. pyrrhorhinos presents a more restricted distribution to Caatinga habitats of Bahia and northern Minas Gerais states (Fig. 9).

Geographic distribution of Wiedomys cerradensis (green, circles) and W. pyrrhorhinos (blue, triangles) showing their corresponding karyotypes according to data from the present study and literature (see text).
The analysis based exclusively on mt-Cytb sequences found weak support for a paraphyletic Wiedomys, with W. pyrrhorhinos more closely related to W. oenax than to W. cerradensis (Supplementary Data SD4), as in the arrangement obtained by Machado et al. (2015). In contrast, the multilocus analysis with a coalescent species tree approach (Fig. 2A) and concatenated nuclear phylogenetic analyses (not shown) recovered strong support for a monophyletic Wiedomys with W. oenax as its sister lineage. Divergence between the 2 genera is recent (Fig. 2B), and the short branch between the common ancestors of Wiedomys and of Wiedomys + Wilfredomys suggests that the diversification of Wiedomys occurred shortly after its separation from Wilfredomys. Successive cladogenetic events separated by a short interval, like those in the Wilfredomys + Wiedomys clade, are more prone to incomplete lineage sorting across the genome during cladogenesis, leading to higher discordance among genes and species trees (Maddison and Knowles 2006; Feng et al. 2022). Under this scenario, the likelihood that a given gene genealogy differs from those of other loci increases as the interval between cladogenetic events becomes shorter and population sizes grow larger. In the present study, the consensus among different loci favors the monophyly of Wiedomys, but divergence within the Wilfredomys + Wiedomys clade deserves greater attention and should be reevaluated using more loci or genomic approaches. Phylogenetic discordance between mitochondrial and nuclear genes is a common occurrence (e.g., Reddy et al. 2017), having been attributed to various factors such as introgressive hybridization, incomplete lineage sorting, selection, or distinct mutation rates in specific genes (Toews and Brelsford 2012). Detailed studies using a representative number of samples from Wilfredomys and other lines of evidence will be necessary to discriminate among these alternatives. We conclude that the multispecies coalescent method applied here is more appropriate to infer the species tree than a single locus, especially when discordance among gene trees is evident (Parada et al. 2021).
Karyotypic diversity
Although with the same diploid number (2n = 62), the W. cerradensis karyotypes reported here can be clearly distinguished from W. pyrrhorhinos due to the presence of a large-sized acrocentric pair and the difference in the number of biarmed and acrocentric pairs reflected in the fundamental numbers (FN = 88 and FN = 96, respectively; Fig. 4).
In addition to the novel karyotypes described herein, another 6 different chromosome complements were previously reported in Wiedomys (Fig. 9). Four of these karyotypes were assigned to W. pyrrhorhinos: (i) 2n = 62, FN = 90 from Caetité (Gonçalves et al. 2005); (ii) 2n = 62, FN = 96 from Curaçá (this study), both in Bahia state; (iii) 2n = 62, FN = 98 to 99 from Minas Gerais state (Geise et al. 2017), and (iv) 2n = 62, FN = 104 from Morro do Chapéu, Bahia state (Souza et al. 2011), and from Canindé do São Francisco and Nossa Senhora da Glória, Sergipe state (Bezerra et al. 2014). Although no comparative banding pattern was performed, the difference between these karyotypes could be related to pericentric inversions or centromere repositioning in the small pairs, or even by different interpretations among authors.
As many as 3 karyotypes have now been described for W. cerradensis: 2n = 60, FN = 88 (holotype, Gonçalves et al. 2005); 2n = 62, FN = 88 from Ceará state (this study); and 2n = 62, FN = 86 from Alagoas (this study) and Pernambuco states (Maia and Langguth 1987; Geise et al. 2010). The difference observed in the FN (86 and 88) for karyotypes with 2n = 62 is probably due to pericentric inversion or centromere repositioning, while the difference found between 2n = 60 and 2n = 62 karyotypes could be due to Robertsonian rearrangements involving the largest acrocentric pair and one medium/small acrocentric.
Despite the changes in the chromosome morphology within Wiedomys altering diploid and fundamental numbers, the phylogenetic and network analyses were unable to detect genetic structure among these samples. We hypothesize that these karyological events have occurred in a relatively short period of time (0.34 to 0.02 Ma; Fig. 2B), considering the results of molecular dating in this study.
A wide diploid number variation can be observed in the tribe Wiedomyini, ranging from 2n = 20 in J. ossitenuis and J. rimofrons, to 2n = 78 in P. ferrugineus (Di-Nizo et al. 2017). Karyotypic changes can play an important role in several evolutionary processes, including speciation (King 1993). First, they can cause meiotic problems as hetero-karyotypes may fail to pair completely, causing meiotic arrest. They may also produce unbalanced gametes through crossovers in rearranged regions or malsegregation during meiotic recombination. In addition, rearrangements such as several pericentric inversions and centric fusion/fission can cause suppression of recombination and reduction in gene flow, leading to the accumulation of incompatibilities fueling the process of speciation (King 1993; Rieseberg 2001; Sumner 2003).
São Francisco River as a putative vicariant barrier
Redefined geographic, genetic, and morphological boundaries between W. cerradensis and W. pyrrhorhinos are coincident with the current course of the São Francisco River, as both species occur on opposite banks of its course, and invite an appraisal of this river as a putative cause of speciation. This hypothesis has been evoked to explain divergence in other Caatinga vertebrate taxa with sister lineages currently separated by the river (Nascimento et al. 2013; Werneck et al. 2015; Bruschi et al. 2019; Recoder and Rodrigues 2020; Thomé et al. 2021). If the river acted as a primary barrier promoting vicariant allopatric speciation in Wiedomys, the splitting date between W. cerradensis and W. pyrrhorhinos, here estimated for the Late Pleistocene, should coincide with the age of formation of the São Francisco modern watercourse dividing the 2 taxa.
The course of the São Francisco River has evolved substantially since its emergence during the Late Cretaceous, when it flowed from Minas Gerais and Bahia states northward, connecting to the Piauí and Parnaíba river basins, and discharging to the equatorial Atlantic Ocean (King 1956; Grabert 1968; Mabesoone 1994; Potter 1997). During the Middle–Late Miocene, the uplift of the Serra Grande and Serra de Ibiapaba Mountains interrupted the northward paleocourse, and the river probably became endorheic, draining its waters into a large lake located at its middle course, in Bahia state (Mabesoone 1994). The river did not achieve its current lower course, making its way to the Brazilian east coast until sometime during the Pliocene–Pleistocene. Mabesoone (1994), based on analyses of the Caatinga limestones formed by the watercourse shift, dated the formation of the modern lower river course to 0.475 to 0.400 Mya, while Auler et al. (2003) proposed that these limestones are much older (>0.500 Mya), possibly of Pliocene–Early Pleistocene origin. No further geological studies have been carried out on the Caatinga limestones to provide a more conclusive date for the formation of the current lower course of the São Francisco River, leaving us to evaluate the 2 ages based on biogeographic evidence alone. This major course shift could have separated populations that were continuously distributed throughout the Caatinga during the endorheic phase, including the ancestor of W. cerradensis and W. pyrrhorhinos. In this case, the divergence date between W. cerradensis and W. pyrrhorhinos is more concordant with a younger formation of the lower course of the São Francisco River, as its 95% lower limit (0.34 Mya) is close to the age proposed by Mabesoone (1994).
Important complementary biogeographic evidence favoring a younger age for the lower river course was provided by Coelho et al. (2022). Analyzing multilocus and genomic data under a coalescent model approach, these authors found the same phylogeographic breaks observed in Wiedomys in another 6 co-distributed vertebrate taxa (3 lizards, 1 frog, 1 bird, and 1 mammal species), with divergence times also close to the 0.475 to 0.400 Mya interval proposed by Mabesoone (1994) for the formation of the lower São Francisco River course. Studies of other vertebrate taxa from the Caatinga found older (2.2 to 1.0 Mya) divergence time estimates for sister lineages separated by the middle course of the São Francisco River midcourse (Siedchlag et al. 2010; Nascimento et al. 2013; Bruschi et al. 2019; Recoder and Rodrigues 2020), suggesting the possibility that different portions of the river promoted divergence at different times, as also recognized by studies on Amazonian rivers (e.g., Gascon et al. 2000; Patton et al. 2000; Leite and Rogers 2013). Nonetheless, in the absence of further geological evidence, the temporal and spatial congruence among Wiedomys and the taxa analyzed by Coelho et al. (2022) suggests that the lower course of the river acted as a vicariant barrier during the Late Pleistocene, promoting divergence in the Caatinga biota.
Final considerations
Our revision based on an integrative approach evidenced that Wiedomys has 2 genetically divergent and morphologically diagnosable species, W. cerradensis and W. pyrrhorhinos, which present much of their geographical limits defined by the São Francisco River. Different chromosome complements were not found in sympatry, but samples of the same species sharing the same karyotype can be less closely related than samples with different karyotypes, corroborating the polymorphic condition of the karyotypes in each species. Despite the karyotype variation in 2n and FN in W. cerradensis (2n = 60, 62, FN = 86, 88) and the karyotype variation in FN in W. pyrrhorhinos (2n = 62, FN = 90, 96, 98, 99, 104), the molecular analyses did not find any population structure within either species. We provide emended descriptions for the species below.
Taxonomic accounts
Wiedomys cerradensisGonçalves, Almeida, and Bonvicino, 2005
Wiedomys cerradensis is a monotypic species, commonly known as: rato-de-nariz-vermelho do Cerrado (Cerrado Red-nosed Mouse), rato-da-fava (Fava mouse), rato-bico-de-lacre (Waxbill mouse), rato-de-palmatória (Paddle mouse), and rato-do-algodão (Cotton mouse; Carvalho 1979).
Type locality
Fazenda Sertão do Formoso (14°37.888ʹS and 45°51.293ʹW), Jaborandi, Bahia state, Brazil (Gonçalves et al. 2005).
Synonyms
Wiedomys cerradensisGonçalves, Almeida, and Bonvicino, 2005; Wiedomys pyrrhorhinus: Gonçalves et al. 2005 [part, samples from Alagoas and Pernambuco states]; Wiedomys pyrrhorhinos: Bonvicino 2015 [part, samples from Alagoas and Pernambuco states].
Emended diagnosis
A relatively small red-nosed mouse of the genus Wiedomys with head-and-body length varying from 72 to 130 mm (Table 4). General dorsal coloration is pale grizzled-brown (relative to W. pyrrhorhinos), but with rump, periocular region, ears, muzzle, manus, and pes covered by bright orange hairs. Conspicuous and broad periocular ring of orangish hairs, in most specimens continuously extending along the infraorbital region to reach the orange muzzle patch. Skull relatively small compared to W. pyrrhorhinos (greatest skull length varying from 22.64 to 31.2 mm), and with a short and pointed rostrum gradually tapering toward its anterior tip. Nasals short, with caudal margins that do not extend posteriorly beyond the frontomaxillary suture.
Summary statistics of external and cranial measurements of Wiedomys species (mean ± standard deviation, minimum and maximum values, and sample size) based on adult specimens (age classes 5 to 7) used in morphometric analyses. Measurements in millimeters (mm), mass in grams (g). Character abbreviation in Fig. S1.
. | Wiedomys cerradensis . | Wiedomys pyrrhorhinos . |
---|---|---|
Head-and-body length | 108.71 ± 11.45 (72 to 130) 99 | 115.2 ± 19.52 (80 to 205) 50 |
Tail length | 165.47 ± 16.53 (119 to 201) 100 | 173.65 ± 25.72 (100 to 211) 49 |
Hindfoot length | 24.71 ± 2.08 (20 to 30) 96 | 26.69 ± 2.49 (19 to 30) 48 |
Ear length | 19.47 ± 2.02 (15 to 30) 96 | 19.83 ± 2.73 (12 to 26) 48 |
Mass | 36.21 ± 9.71 (11 to 60) 99 | 40.84 ± 11 (18 to 70) 47 |
GSL | 28.74 ± 1.49 (22.64 to 31.20) 106 | 30.35 ± 1.24 (26.15 to 34.27) 59 |
NL | 10.28 ± 0.94 (7.10 to 12.75) 106 | 11.26 ± 1.01 (7.77 to 14.50) 59 |
RB | 3.56 ± 0.31 (2.96 to 4.47) 106 | 3.72 ± 0.35 (3.21 to 4.77) 59 |
AB | 8.34 ± 0.65 (5.58 to 9.55) 106 | 8.76 ± 0.52 (7.60 to 9.90) 59 |
LIB | 4.42 ± 0.2 (3.79 to 4.96) 106 | 4.61 ± 0.2 (4.18 to 5.08) 59 |
BB | 12.79 ± 0.56 (10.19 to 14.10) 106 | 13.34 ± 0.67 (9.91 to 14.58) 59 |
IPB | 9.71 ± 0.63 (8.13 to 11.67) 106 | 10.17 ± 0.56 (9.04 to 11.35) 59 |
IPL | 3.88 ± 0.44 (2.98 to 5.15) 106 | 4.19 ± 0.44 (3.23 to 5.28) 59 |
PL | 10.96 ± 0.8 (7.70 to 13.25) 106 | 11.72 ± 0.61 (10.31 to 13.20) 59 |
IFL | 5.58 ± 0.61 (3.57 to 7.26) 106 | 5.75 ± 0.52 (4.25 to 6.67) 59 |
PBL | 4.47 ± 0.38 (3.37 to 5.34) 106 | 4.99 ± 0.33 (4.39 to 5.95) 59 |
LM | 4.45 ± 0.18 (3.59 to 4.86) 106 | 4.65 ± 0.21 (4.15 to 5.10) 59 |
M1M | 5.09 ± 0.24 (4.25 to 5.66) 106 | 5.23 ± 0.29 (4.46 to 5.91) 59 |
ABD | 4.42 ± 0.45 (3.21 to 5.41) 106 | 4.73 ± 0.47 (3.01 to 5.62) 59 |
ABB | 4.51 ± 0.35 (3.13 to 5.18) 106 | 4.82 ± 0.43 (4.06 to 5.97) 59 |
ZPL | 2.75 ± 0.31 (2.07 to 3.64) 106 | 2.89 ± 0.4 (2.07 to 3.86) 59 |
ZB | 14.80 ± 0.82 (11.53 to 16.64) 106 | 15.49 ± 0.78 (13.48 to 17.23) 59 |
OL | 9.76 ± 0.66 (8.13 to 11.48) 106 | 10.31 ± 0.54 (8.77 to 11.28) 59 |
BD | 9.53 ± 0.64 (7.59 to 11.12) 106 | 9.94 ± 0.57 (8.06 to 11.31) 59 |
ML | 14.58 ± 0.99 (10.08 to 16.55) 106 | 15.38 ± 0.75 (13.77 to 17.07) 59 |
. | Wiedomys cerradensis . | Wiedomys pyrrhorhinos . |
---|---|---|
Head-and-body length | 108.71 ± 11.45 (72 to 130) 99 | 115.2 ± 19.52 (80 to 205) 50 |
Tail length | 165.47 ± 16.53 (119 to 201) 100 | 173.65 ± 25.72 (100 to 211) 49 |
Hindfoot length | 24.71 ± 2.08 (20 to 30) 96 | 26.69 ± 2.49 (19 to 30) 48 |
Ear length | 19.47 ± 2.02 (15 to 30) 96 | 19.83 ± 2.73 (12 to 26) 48 |
Mass | 36.21 ± 9.71 (11 to 60) 99 | 40.84 ± 11 (18 to 70) 47 |
GSL | 28.74 ± 1.49 (22.64 to 31.20) 106 | 30.35 ± 1.24 (26.15 to 34.27) 59 |
NL | 10.28 ± 0.94 (7.10 to 12.75) 106 | 11.26 ± 1.01 (7.77 to 14.50) 59 |
RB | 3.56 ± 0.31 (2.96 to 4.47) 106 | 3.72 ± 0.35 (3.21 to 4.77) 59 |
AB | 8.34 ± 0.65 (5.58 to 9.55) 106 | 8.76 ± 0.52 (7.60 to 9.90) 59 |
LIB | 4.42 ± 0.2 (3.79 to 4.96) 106 | 4.61 ± 0.2 (4.18 to 5.08) 59 |
BB | 12.79 ± 0.56 (10.19 to 14.10) 106 | 13.34 ± 0.67 (9.91 to 14.58) 59 |
IPB | 9.71 ± 0.63 (8.13 to 11.67) 106 | 10.17 ± 0.56 (9.04 to 11.35) 59 |
IPL | 3.88 ± 0.44 (2.98 to 5.15) 106 | 4.19 ± 0.44 (3.23 to 5.28) 59 |
PL | 10.96 ± 0.8 (7.70 to 13.25) 106 | 11.72 ± 0.61 (10.31 to 13.20) 59 |
IFL | 5.58 ± 0.61 (3.57 to 7.26) 106 | 5.75 ± 0.52 (4.25 to 6.67) 59 |
PBL | 4.47 ± 0.38 (3.37 to 5.34) 106 | 4.99 ± 0.33 (4.39 to 5.95) 59 |
LM | 4.45 ± 0.18 (3.59 to 4.86) 106 | 4.65 ± 0.21 (4.15 to 5.10) 59 |
M1M | 5.09 ± 0.24 (4.25 to 5.66) 106 | 5.23 ± 0.29 (4.46 to 5.91) 59 |
ABD | 4.42 ± 0.45 (3.21 to 5.41) 106 | 4.73 ± 0.47 (3.01 to 5.62) 59 |
ABB | 4.51 ± 0.35 (3.13 to 5.18) 106 | 4.82 ± 0.43 (4.06 to 5.97) 59 |
ZPL | 2.75 ± 0.31 (2.07 to 3.64) 106 | 2.89 ± 0.4 (2.07 to 3.86) 59 |
ZB | 14.80 ± 0.82 (11.53 to 16.64) 106 | 15.49 ± 0.78 (13.48 to 17.23) 59 |
OL | 9.76 ± 0.66 (8.13 to 11.48) 106 | 10.31 ± 0.54 (8.77 to 11.28) 59 |
BD | 9.53 ± 0.64 (7.59 to 11.12) 106 | 9.94 ± 0.57 (8.06 to 11.31) 59 |
ML | 14.58 ± 0.99 (10.08 to 16.55) 106 | 15.38 ± 0.75 (13.77 to 17.07) 59 |
Summary statistics of external and cranial measurements of Wiedomys species (mean ± standard deviation, minimum and maximum values, and sample size) based on adult specimens (age classes 5 to 7) used in morphometric analyses. Measurements in millimeters (mm), mass in grams (g). Character abbreviation in Fig. S1.
. | Wiedomys cerradensis . | Wiedomys pyrrhorhinos . |
---|---|---|
Head-and-body length | 108.71 ± 11.45 (72 to 130) 99 | 115.2 ± 19.52 (80 to 205) 50 |
Tail length | 165.47 ± 16.53 (119 to 201) 100 | 173.65 ± 25.72 (100 to 211) 49 |
Hindfoot length | 24.71 ± 2.08 (20 to 30) 96 | 26.69 ± 2.49 (19 to 30) 48 |
Ear length | 19.47 ± 2.02 (15 to 30) 96 | 19.83 ± 2.73 (12 to 26) 48 |
Mass | 36.21 ± 9.71 (11 to 60) 99 | 40.84 ± 11 (18 to 70) 47 |
GSL | 28.74 ± 1.49 (22.64 to 31.20) 106 | 30.35 ± 1.24 (26.15 to 34.27) 59 |
NL | 10.28 ± 0.94 (7.10 to 12.75) 106 | 11.26 ± 1.01 (7.77 to 14.50) 59 |
RB | 3.56 ± 0.31 (2.96 to 4.47) 106 | 3.72 ± 0.35 (3.21 to 4.77) 59 |
AB | 8.34 ± 0.65 (5.58 to 9.55) 106 | 8.76 ± 0.52 (7.60 to 9.90) 59 |
LIB | 4.42 ± 0.2 (3.79 to 4.96) 106 | 4.61 ± 0.2 (4.18 to 5.08) 59 |
BB | 12.79 ± 0.56 (10.19 to 14.10) 106 | 13.34 ± 0.67 (9.91 to 14.58) 59 |
IPB | 9.71 ± 0.63 (8.13 to 11.67) 106 | 10.17 ± 0.56 (9.04 to 11.35) 59 |
IPL | 3.88 ± 0.44 (2.98 to 5.15) 106 | 4.19 ± 0.44 (3.23 to 5.28) 59 |
PL | 10.96 ± 0.8 (7.70 to 13.25) 106 | 11.72 ± 0.61 (10.31 to 13.20) 59 |
IFL | 5.58 ± 0.61 (3.57 to 7.26) 106 | 5.75 ± 0.52 (4.25 to 6.67) 59 |
PBL | 4.47 ± 0.38 (3.37 to 5.34) 106 | 4.99 ± 0.33 (4.39 to 5.95) 59 |
LM | 4.45 ± 0.18 (3.59 to 4.86) 106 | 4.65 ± 0.21 (4.15 to 5.10) 59 |
M1M | 5.09 ± 0.24 (4.25 to 5.66) 106 | 5.23 ± 0.29 (4.46 to 5.91) 59 |
ABD | 4.42 ± 0.45 (3.21 to 5.41) 106 | 4.73 ± 0.47 (3.01 to 5.62) 59 |
ABB | 4.51 ± 0.35 (3.13 to 5.18) 106 | 4.82 ± 0.43 (4.06 to 5.97) 59 |
ZPL | 2.75 ± 0.31 (2.07 to 3.64) 106 | 2.89 ± 0.4 (2.07 to 3.86) 59 |
ZB | 14.80 ± 0.82 (11.53 to 16.64) 106 | 15.49 ± 0.78 (13.48 to 17.23) 59 |
OL | 9.76 ± 0.66 (8.13 to 11.48) 106 | 10.31 ± 0.54 (8.77 to 11.28) 59 |
BD | 9.53 ± 0.64 (7.59 to 11.12) 106 | 9.94 ± 0.57 (8.06 to 11.31) 59 |
ML | 14.58 ± 0.99 (10.08 to 16.55) 106 | 15.38 ± 0.75 (13.77 to 17.07) 59 |
. | Wiedomys cerradensis . | Wiedomys pyrrhorhinos . |
---|---|---|
Head-and-body length | 108.71 ± 11.45 (72 to 130) 99 | 115.2 ± 19.52 (80 to 205) 50 |
Tail length | 165.47 ± 16.53 (119 to 201) 100 | 173.65 ± 25.72 (100 to 211) 49 |
Hindfoot length | 24.71 ± 2.08 (20 to 30) 96 | 26.69 ± 2.49 (19 to 30) 48 |
Ear length | 19.47 ± 2.02 (15 to 30) 96 | 19.83 ± 2.73 (12 to 26) 48 |
Mass | 36.21 ± 9.71 (11 to 60) 99 | 40.84 ± 11 (18 to 70) 47 |
GSL | 28.74 ± 1.49 (22.64 to 31.20) 106 | 30.35 ± 1.24 (26.15 to 34.27) 59 |
NL | 10.28 ± 0.94 (7.10 to 12.75) 106 | 11.26 ± 1.01 (7.77 to 14.50) 59 |
RB | 3.56 ± 0.31 (2.96 to 4.47) 106 | 3.72 ± 0.35 (3.21 to 4.77) 59 |
AB | 8.34 ± 0.65 (5.58 to 9.55) 106 | 8.76 ± 0.52 (7.60 to 9.90) 59 |
LIB | 4.42 ± 0.2 (3.79 to 4.96) 106 | 4.61 ± 0.2 (4.18 to 5.08) 59 |
BB | 12.79 ± 0.56 (10.19 to 14.10) 106 | 13.34 ± 0.67 (9.91 to 14.58) 59 |
IPB | 9.71 ± 0.63 (8.13 to 11.67) 106 | 10.17 ± 0.56 (9.04 to 11.35) 59 |
IPL | 3.88 ± 0.44 (2.98 to 5.15) 106 | 4.19 ± 0.44 (3.23 to 5.28) 59 |
PL | 10.96 ± 0.8 (7.70 to 13.25) 106 | 11.72 ± 0.61 (10.31 to 13.20) 59 |
IFL | 5.58 ± 0.61 (3.57 to 7.26) 106 | 5.75 ± 0.52 (4.25 to 6.67) 59 |
PBL | 4.47 ± 0.38 (3.37 to 5.34) 106 | 4.99 ± 0.33 (4.39 to 5.95) 59 |
LM | 4.45 ± 0.18 (3.59 to 4.86) 106 | 4.65 ± 0.21 (4.15 to 5.10) 59 |
M1M | 5.09 ± 0.24 (4.25 to 5.66) 106 | 5.23 ± 0.29 (4.46 to 5.91) 59 |
ABD | 4.42 ± 0.45 (3.21 to 5.41) 106 | 4.73 ± 0.47 (3.01 to 5.62) 59 |
ABB | 4.51 ± 0.35 (3.13 to 5.18) 106 | 4.82 ± 0.43 (4.06 to 5.97) 59 |
ZPL | 2.75 ± 0.31 (2.07 to 3.64) 106 | 2.89 ± 0.4 (2.07 to 3.86) 59 |
ZB | 14.80 ± 0.82 (11.53 to 16.64) 106 | 15.49 ± 0.78 (13.48 to 17.23) 59 |
OL | 9.76 ± 0.66 (8.13 to 11.48) 106 | 10.31 ± 0.54 (8.77 to 11.28) 59 |
BD | 9.53 ± 0.64 (7.59 to 11.12) 106 | 9.94 ± 0.57 (8.06 to 11.31) 59 |
ML | 14.58 ± 0.99 (10.08 to 16.55) 106 | 15.38 ± 0.75 (13.77 to 17.07) 59 |
Distribution
Wiedomys cerradensis occurs in the Caatinga and Cerrado biomes. Occupies the left bank of the São Francisco River from the northwest Minas Gerais state, through southeast Goiás state, and south Tocantins state to the central-eastern region of Maranhão state and the Ceará state, expanding eastwards through Pernambuco and Alagoas states.
Fossils
Pardiñas and Barbière (2018) demonstrated that the fossil species from Argentina (Cholomys pearsoni and Wiedomys marplatensis), previously considered either allied to or included in Wiedomys by Reig (1980) and Quintana (2002), lack the diagnostic dental characters of Wiedomyini and should not be included in this tribe. If this hypothesis is accepted, the fossil record of Wiedomys is limited to remnants found in limestone caves from Bahia and Piauí states in Brazil. Neves et al. (2017) reported specimens identified as Wiedomys sp. from Serra da Capivara caves, at Piauí state, associated with dated materials of Late Pleistocene (~26,000 years ago) to Holocene (~1,670 years ago) ages. We provisionally assign those specimens to W. cerradensis based on the geographic distribution of this species and on the fact that the specimen illustrated in Neves et al. (2017: Fig. 3d) exhibits a broad anteromedian cingulum in M1, a condition most commonly seen in W. cerradensis.
Wiedomys pyrrhorhinos (Wied in Schinz 1821)
Wiedomys pyrrhorhinos is a monotypic species, commonly known as: rato-de-nariz-vermelho da Caatinga (Caatinga Red-nosed Mouse), rato-da-fava (Fava mouse), rato-bico-de-lacre (Waxbill mouse), rato-de-palmatória (Paddle mouse), and rato-do-algodão (Cotton mouse; Carvalho 1979).
Type locality
Ribeirão da Ressaca (14°51ʹS, 41°24ʹW), state of Bahia, Brazil. The Ribeirão da Ressaca, formerly known “Riacho da Ressaca,” is a short tributary of the Rio Gavião, in Bahia state, near the border with Minas Gerais state, flowing from the municipality of Ilha Dentro to the neighboring municipality of Tremedal. Prince Maximilian Alexander Philip of Wied-Neuwied (hereafter Wied, in accordance with Vanzolini and Myers 2015) collected the holotype of W. pyrrhorhinos in the “caatingas along the Riacho da Ressaca” while traveling between the farms of “Tamboril” and “Ilha” (Avila-Pires 1965), areas that are now part of the municipalities of Tremedal and Ilha Dentro, respectively (Bockermann 1957). Wied reported that W. pyrrhorhinos was found inhabiting one of the chambers of a nest of the Rufous-fronted Thornbird (Phallocedomus rufifrons rufifrons), a species also described by Wied (as Anabates rufifronsWied 1821) based on specimens collected during the same trip between “Tamboril” and “Ilha” (Wied 1821). The type locality of W. pyrrhorhinos assumed by us, thus, follows the same type-locality restriction proposed by LeCroy and Sloss (2000) for A. rufifronsWied 1821.
Correct spelling of the specific epithet
The correct spelling of the scientific name of the Caatinga Red-nosed Mouse has been a matter of controversy, assuming 3 different forms in recent taxonomic publications: pyrrhorinos (e.g., Pardiñas 2017), pyrrhorhinos (e.g., Bonvicino 2015), and pyrrhorhinus (e.g., Gonçalves et al. 2005). The spelling pyrrhorinos was used by Wied in a short description of the Caatinga Red-nosed Mouse in the second volume of his book “Reise nach Brasilien in den Jahren 1815 bis 1817” (Wied 1821). In the same year, Schinz (1821) published another description of the same species, crediting Wied as its author (“Mus pyrrhorhinos Princ. Max.”) but using the alternative spelling pyrrhorhinos. This spelling was published in the first volume of Schinz’ book “Das Thierreich, eingetheilt nach dem Bau der Thiere als Grundlage ihrer Naturgeschichte und der vergleichenden Anatomie von den Herrn Ritter von Cuvier, Erster: Band Säugethiere und Vögel,” and was adopted by most subsequent authors (Hershkovitz 1959; Cabrera 1961; Avila-Pires 1965; Honacki et al. 1982; Maia and Langguth 1987; Corbet and Hill 1991; Musser and Carleton 2005; Bonvicino 2015). Until 2023 there was no way to establish priority between the 2 spellings, both of which were published in 1821, but in 2023 it was reported that the first volume of Schinz’ book was published in October 1821, before the second volume of Wied’s book, which was published in December 1821 (Nascimento and Garbino 2023). Therefore, the name published in Schinz’ book has priority over the one published in Wied’s and the correct spelling of the Caatinga Red-nosed Mouse is Wiedomys pyrrhorhinos (Wied in Schinz 1821). The latinization of Schinz’ spelling made by Wied in subsequent publications (Wied 1823, 1826), and followed by several authors (see synonyms) is considered unjustified according to the International Code of Zoological Nomenclature (Article 33.2.3.1). Interestingly, Wied latinized Schinz’ epithet pyrrhorhinos instead of his own epithet pyrrhorinos, suggesting the lack of an “h” in the epithet originally published in his “Reise nach Brasilien” was a printing error.
Synonyms
Mus pyrrhorhinos Wied in Schinz (1821) [original description]; Mus pyrrhorinosWied (1821) [incorrect spelling]; Mus pyrrhorhinusWied 1823 [Latinization of Schinz’ pyrrhorhinos, unjustified emendation]; Hesperomys pyrrhorhinus: Burmeister 1856 [new name combination]; Hesperomys (Rhipidomys) pyrrhorhinus: Thomas 1882 [new name combination]; Oryzomys pyrrhorhinus: Thomas 1886 [new name combination]; Thomasomys pyrrhorinos: Moojen 1952 [new name combination of Wied’s incorrect spelling]; Wiedomys pyrrhorhinos: Hershkovitz 1959 [current name combination]; Wiedomys pirrhorhynos: Pardiñas 2017 [incorrect spelling].
Emended diagnosis
A relatively large red-nosed mouse of the genus Wiedomys with head-and-body length varying from 80 to 205 mm (Table 4). General dorsal coloration grizzled-brown, but with rump, periocular region, ears, muzzle, manus, and pes covered by bright orange hairs. Narrow or incomplete periocular ring of orangish hairs, separated from the orangish muzzle patch by a strip of grizzled hairs along the infraorbital region. Skull relatively larger (greatest skull length ranging from 26.15 to 34.27 mm) and with a long and blunt rostrum. Nasals are long, with pointed caudal margins that extend posteriorly beyond the frontomaxillary suture.
Distribution
Wiedomys pyrrhorhinos is endemic to Brazil and to the Caatinga biome. It is distributed from the north Minas Gerais state, extending through Bahia to Sergipe states, on the right bank of the São Francisco River.
Fossils
Gomes et al. (2020) documented specimens of W. pyrrhorhinos recovered from owl pellets collected in the Toca dos Ossos cave of Bahia state, but they have indeterminate age.
Supplementary data
Supplementary data are available at Journal of Mammalogy online.
Supplementary Data SD1. Ingroup and outgroup sequences extracted from GenBank used for phylogenetic analyses: species, mitochondrial gene (mt-Cytb), and nuclear genes (IRBP and i7FGB).
Supplementary Data SD2. Craniodental measurements of Wiedomys used in quantitative morphological analyses.
Supplementary Data SD3. Gene trees obtained from the different partitions of the multilocus data set by Bayesian multispecies coalescent analysis.
Supplementary Data SD4. Phylogenetic tree based on Bayesian analysis using mt-Cytb sequences. Maximum likelihood analysis recovered a similar topology. Numbers close to branches are bootstrap values followed by posterior probability (PP) values. The sign “-” indicates absence of bootstrap in maximum likelihood due to collapsed phylogenetic branches.
Acknowledgments
We thank the following curators and technicians for the access and loan of specimens under their care: João Alves de Oliveira, Marcelo Weskler, and Aldo Caccavo de Araujo (MN/UFRJ); Cláudia Guimarães Costa and Albert Carl Cavalcante (PUC-Minas); Jader Marinho-Filho and Pedro de Podestá (UNB). We also thank Gabriel Marroig (USP), Alfredo Langguth (UFPB), and Juliana Bragança Campos (UNB) for providing tissues from specimens used in this study, Renata Cecília Amaro for the cytogenetic preparations, and Miguel T. Rodrigues and his team for some of the samples from Bahia, Tocantins, Piauí, and Pernambuco states. We are also indebted to Anna Ludmilla C. P. Nascimento and Mariana Dias Guilardi for helping with field trips and the field team of the Laboratório de Biologia e Parasitologia de Mamíferos Silvestres Reservatórios, IOC/FIOCRUZ. We also thank Regiane Spirandelli and Leonardo Kobashi for technical assistance. We are also indebted to Ulyses F. J. Pardiñas and an anonymous reviewer for important and constructive criticisms to a previous version of this paper.
Author contributions
CBD-N: conceptualization, formal analysis, investigation, methodology, writing—original draft; AL: conceptualization, formal analysis, investigation, methodology, writing—original draft; CAC-F: conceptualization, formal analysis, investigation, methodology, writing—original draft; MJJS: conceptualization, data curation, funding acquisition, supervision, writing—original draft; AMRB: data curation, writing—original draft; EYS-V: formal analysis, investigation, methodology, writing—review & editing; CRB: conceptualization, data curation, funding acquisition, supervision, writing—original draft; LMP: conceptualization, data curation, funding acquisition, supervision, writing—original draft; PRG: conceptualization, data curation, funding acquisition, supervision, writing—original draft.
Funding
This study was funded in part by Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ grants n° E26/102.804/2011, E26/201/200/2014, FAPERJ No. 08/2020 and E-26/200.415/2023), Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP: 2014/02885-2 for MJJS), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brazil (CAPES)—Finance Code 001, CAPES/PNPD, and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (grants n° 305564/2010-2, 307669/2013-0, 313686/2020-3, 300980/2022-1, and 200533/2022-3).
Conflict of interest
None declared.
Data availability
The data sets generated during the current study are available in GenBank.
References
Appendix I
Specimens of Wiedomys examined in morphological, cytogenetic, and molecular analyses.
Reg. number . | Species . | SF riverside . | OTU . | Gazetteer . | Locality . | State . | Lat100 . | Long100 . | Morphological data . | Genetic data . | GenBank number . |
---|---|---|---|---|---|---|---|---|---|---|---|
JBC16 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953694; PP953717 | |
JBC18 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953690; PP953725 | |
JBC26 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953693; PP953715 | |
MCN-M1968 | W. pyrrhorhinos | Right | Berilo | 2 | Leme do Prado | MG | −17,08 | −42,69 | x | ||
MCN-M1507 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M1700 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2013 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2262 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73314 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73416 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73419 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73431 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73435 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73437 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73438 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73442 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73453 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73461 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73477 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73520 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN−M1053 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MCN−M1054 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MN68601 | W. pyrrhorhinos | Right | Caetité | 10 | Piripá | BA | −14,93 | −41,72 | x | ||
MN18441 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18442 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18725 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18726 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18727 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18756 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18758 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60780 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60783 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60784 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN63357 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | i7Fgb | PP953713 |
MN63420 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | mt-Cytb; i7Fgb | PP953695; PP953709 |
MN18527 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18528 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18529 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18530 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18531 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18532 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18698 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18699 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18700 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18701 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MN18702 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MTR2980 | W. pyrrhorhinos | Right | Caetité | 15 | Santo Inácio | BA | −11,10 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953698; PP953731; PP953648 | |
UFPB9790 | W. pyrrhorhinos | Right | Canindé de São Francisco | 21 | Nossa Senhora da Glória | SE | −10,21 | −37,42 | mt-Cytb; i7Fgb | PP953705; PP953714 | |
UFPB9780 | W. pyrrhorhinos | Right | Canindé de São Francisco | 22 | Monte Alegre de Sergipe | SE | −10,03 | −37,56 | mt-Cytb; i7Fgb | PP953702; PP953716 | |
MUFAL0265/MJJS459 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; i7Fgb; IRBP | PP953704; PP953732; PP953646 | |
UFPB9764/ARB788 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | mt-Cytb | PP953706 |
UNB2761 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2764 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2801 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
CIT1017 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953699; PP953730; PP953661 | |
CIT959 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; IRBP | PP953700; PP953644 | |
CIT961 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953691; PP953733; PP953645 | |
LBCE5202 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb | PP953701; PP953710 | |
MUFAL0283/MJJS486 | W. pyrrhorhinos | Right | Canindé de São Francisco | 25 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; IRBP | PP953703, PP953647 | |
MN76145 | W. pyrrhorhinos | Right | Berilo | 5 | Juramento | BA | −16,85 | −43,58 | x | mt-Cytb | PP953696 |
MCN-M2182 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,91 | −42,60 | x | ||
MCN-M1511 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2459 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2893 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2902 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2945 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2952 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M1052 | W. pyrrhorhinos | Right | Berilo | 7 | Grao Mogol | MG | −16,56 | −42,89 | x | ||
MCN-M2699 | W. pyrrhorhinos | Right | Berilo | 8 | Porteirinha | MG | −15,74 | −43,03 | x | ||
MN34412 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN34413 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62180 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62181 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN18751 | W. pyrrhorhinos | Right | Morro do Chapéu | 16 | Palmeiras | BA | −12,52 | −41,55 | x | ||
MN18428 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18498 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18502 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18503 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18506 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18508 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18509 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18510 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18511 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18512 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18513 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18516 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18517 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18521 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18522 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18523 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18525 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60772 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60778 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN71607 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapeu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953697; PP953712 |
MN71608 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapéu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953692; PP953711 |
MN18715 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18716 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18717 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18718 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18719 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18720 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18723 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18760 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18761 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18762 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18763 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18764 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18765 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60791 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60792 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60793 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN11661 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18445 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18752 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18753 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18754 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18755 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN60789 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18454 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18457 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18459 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18460 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18461 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18463 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18466 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18468 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18469 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18470 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18474 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18475 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18476 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18477 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18480 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18481 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18482 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18483 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18484 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18485 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18486 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18622 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18624 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
MN18656 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
UFPB4043 | W. cerradensis | Left | Caruaru | 39 | Bezerros | PE | −9,17 | −37,37 | mt-Cytb; i7Fgb | PP953678, PP953708 | |
CIT1680/SA01 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953665; PP953659; PP953729 | |
CIT1681/SA02 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953677; PP953741; 953,660 | |
MN18586 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18587 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18588 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18745 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18747 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41412 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN25456 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41413 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN60756 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60757 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60761 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60763 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18451 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18496 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18592 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60752 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60753 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60754 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
UNB2710 | W. cerradensis | Left | Ceará | 43 | Jardim | CE | −7,58 | −39,30 | x | ||
MN18790 | W. cerradensis | Left | Ceará | 44 | Crato | CE | −8,23 | −39,67 | x | ||
MN17449 | W. cerradensis | Left | Ceará | 45 | Missao Velha | CE | −7,23 | −39,13 | x | ||
MN18808 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60563 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60568 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60561 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,23 | −39,13 | x | ||
MN18729 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN18789 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60559 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60560 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
LBCE13942 | W. cerradensis | Left | Ceará | 47 | Russas | CE | −4,93 | −37,97 | mt-Cytb; i7Fgb | PP953679; PP953718 | |
LBCE10412 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953672; PP953723 | |
LBCE5255 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953670; PP953707 | |
MN1531 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1532 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1764 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN60657 | W. cerradensis | Left | Ceará | 50 | Guaraciaba do Norte | CE | −41,67 | −40,75 | x | ||
MN18737 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18738 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18739 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60569 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60654 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18544 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18546 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18548 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18549 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18550 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18551 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18552 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18553 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18554 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18555 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18556 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18557 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18558 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18559 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18560 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18561 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18562 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18563 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18564 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18669 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18670 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18671 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18672 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18673 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18674 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18676 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18677 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18678 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18680 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18681 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18741 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18800 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18802 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18803 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18805 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18806 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN27213 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
UNB2594 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953721 |
UNB2595 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953722 |
MN71267 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,89 | x | ||
MRT3874 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,60 | −47,89 | mt-Cytb; IRBP | PP953685; PP953664 | |
CRB2716 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953689 | |
CRB2718 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb; i7Fgb | PP953686; PP953724 | |
CRB2729 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953688 | |
MN81688 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN81694 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN4169 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN4170 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN67022 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | i7Fgb | PP953726 |
MN67023 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1614 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1617 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB2064 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1776 | W. cerradensis | Left | Jaborandi | 63 | Formoso | MG | −14,95 | −46,23 | x | ||
MN61657 | W. cerradensis | Left | Jaborandi | 63 | Jaborandi | BA | −13,62 | −44,44 | i7Fgb | PP953720 | |
MN83081 | W. cerradensis | Left | Maranhão | 56 | Mirador | MA | −6,36 | −44,35 | x | i7Fgb | PP953728 |
LEM63 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953681; PP953719 | |
LEM75 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953683; PP953727 | |
MN18491 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18589 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18590 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18684 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18742 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18743 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18744 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18746 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18796 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18798 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18799 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18591 | W. cerradensis | Left | Pesqueira | 36 | Belo Jardim | PE | −8,33 | −36,42 | x | ||
MN18613 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18675 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18679 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18682 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
UNB2706 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
UNB2715 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
MN75110 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75111 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75126 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
MN75144 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
CIT1708 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953674; PP953739; PP953649 | |
MZUSP30453/UUPI174 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953687; PP953742; PP953652 | |
MUFAL0249/MJJS414 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | ||
MUFAL0250/MJJS415 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | mt-Cytb; i7Fgb; IRBP | PP953669; PP953744; PP953643 | |
MUFAL0255/MJJS431 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | mt-Cytb; i7Fgb; IRBP | PP953682; PP953740; PP953653 |
MUFAL0179/ALN294 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; IRBP | PP953666; PP953656 | |
MUFAL0180/ALN295 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | x | mt-Cytb; IRBP | PP953676; PP953651 |
MUFAL0184/ALN299 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953675; PP953734; PP953657 | |
MUFAL0190/ALN305 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953667; PP953736; PP953663 | |
MUFAL0195/ALN310 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953671; PP953738; PP953650 | |
MUFAL0199/ALN314 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953673; PP953743; PP953658 | |
MUFAL0182/ALN297 | W. cerradensis | Left | Piranhas | 27 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953668; PP953735; PP953654 | |
UNB2762 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
UNB2763 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
MUFAL0286/MJJS489 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; IRBP | PP953684; PP953655 | |
MUFAL0287/MJJS490 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; i7Fgb; IRBP | PP953680; PP953737; PP953662 | |
MN18776 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18778 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18779 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18780 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18781 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18782 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18783 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18784 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18785 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18786 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18787 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18493 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18593 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18598 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18599 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18688 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18689 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN17382 | W. cerradensis | Left | Quebrangulo | 31 | Palmeira dos Índios | AL | −9,40 | −36,70 | x | ||
MN18788 | W. cerradensis | Left | Quebrangulo | 32 | Limoeiro de Anadia | AL | −9,73 | −36,50 | x | ||
MN18594 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18690 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18767 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18768 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18769 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18771 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18773 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18811 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x |
Reg. number . | Species . | SF riverside . | OTU . | Gazetteer . | Locality . | State . | Lat100 . | Long100 . | Morphological data . | Genetic data . | GenBank number . |
---|---|---|---|---|---|---|---|---|---|---|---|
JBC16 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953694; PP953717 | |
JBC18 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953690; PP953725 | |
JBC26 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953693; PP953715 | |
MCN-M1968 | W. pyrrhorhinos | Right | Berilo | 2 | Leme do Prado | MG | −17,08 | −42,69 | x | ||
MCN-M1507 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M1700 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2013 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2262 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73314 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73416 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73419 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73431 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73435 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73437 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73438 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73442 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73453 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73461 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73477 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73520 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN−M1053 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MCN−M1054 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MN68601 | W. pyrrhorhinos | Right | Caetité | 10 | Piripá | BA | −14,93 | −41,72 | x | ||
MN18441 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18442 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18725 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18726 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18727 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18756 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18758 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60780 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60783 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60784 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN63357 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | i7Fgb | PP953713 |
MN63420 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | mt-Cytb; i7Fgb | PP953695; PP953709 |
MN18527 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18528 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18529 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18530 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18531 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18532 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18698 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18699 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18700 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18701 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MN18702 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MTR2980 | W. pyrrhorhinos | Right | Caetité | 15 | Santo Inácio | BA | −11,10 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953698; PP953731; PP953648 | |
UFPB9790 | W. pyrrhorhinos | Right | Canindé de São Francisco | 21 | Nossa Senhora da Glória | SE | −10,21 | −37,42 | mt-Cytb; i7Fgb | PP953705; PP953714 | |
UFPB9780 | W. pyrrhorhinos | Right | Canindé de São Francisco | 22 | Monte Alegre de Sergipe | SE | −10,03 | −37,56 | mt-Cytb; i7Fgb | PP953702; PP953716 | |
MUFAL0265/MJJS459 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; i7Fgb; IRBP | PP953704; PP953732; PP953646 | |
UFPB9764/ARB788 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | mt-Cytb | PP953706 |
UNB2761 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2764 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2801 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
CIT1017 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953699; PP953730; PP953661 | |
CIT959 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; IRBP | PP953700; PP953644 | |
CIT961 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953691; PP953733; PP953645 | |
LBCE5202 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb | PP953701; PP953710 | |
MUFAL0283/MJJS486 | W. pyrrhorhinos | Right | Canindé de São Francisco | 25 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; IRBP | PP953703, PP953647 | |
MN76145 | W. pyrrhorhinos | Right | Berilo | 5 | Juramento | BA | −16,85 | −43,58 | x | mt-Cytb | PP953696 |
MCN-M2182 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,91 | −42,60 | x | ||
MCN-M1511 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2459 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2893 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2902 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2945 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2952 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M1052 | W. pyrrhorhinos | Right | Berilo | 7 | Grao Mogol | MG | −16,56 | −42,89 | x | ||
MCN-M2699 | W. pyrrhorhinos | Right | Berilo | 8 | Porteirinha | MG | −15,74 | −43,03 | x | ||
MN34412 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN34413 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62180 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62181 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN18751 | W. pyrrhorhinos | Right | Morro do Chapéu | 16 | Palmeiras | BA | −12,52 | −41,55 | x | ||
MN18428 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18498 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18502 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18503 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18506 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18508 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18509 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18510 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18511 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18512 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18513 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18516 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18517 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18521 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18522 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18523 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18525 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60772 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60778 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN71607 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapeu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953697; PP953712 |
MN71608 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapéu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953692; PP953711 |
MN18715 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18716 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18717 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18718 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18719 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18720 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18723 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18760 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18761 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18762 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18763 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18764 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18765 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60791 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60792 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60793 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN11661 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18445 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18752 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18753 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18754 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18755 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN60789 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18454 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18457 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18459 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18460 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18461 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18463 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18466 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18468 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18469 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18470 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18474 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18475 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18476 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18477 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18480 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18481 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18482 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18483 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18484 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18485 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18486 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18622 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18624 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
MN18656 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
UFPB4043 | W. cerradensis | Left | Caruaru | 39 | Bezerros | PE | −9,17 | −37,37 | mt-Cytb; i7Fgb | PP953678, PP953708 | |
CIT1680/SA01 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953665; PP953659; PP953729 | |
CIT1681/SA02 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953677; PP953741; 953,660 | |
MN18586 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18587 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18588 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18745 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18747 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41412 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN25456 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41413 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN60756 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60757 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60761 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60763 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18451 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18496 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18592 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60752 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60753 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60754 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
UNB2710 | W. cerradensis | Left | Ceará | 43 | Jardim | CE | −7,58 | −39,30 | x | ||
MN18790 | W. cerradensis | Left | Ceará | 44 | Crato | CE | −8,23 | −39,67 | x | ||
MN17449 | W. cerradensis | Left | Ceará | 45 | Missao Velha | CE | −7,23 | −39,13 | x | ||
MN18808 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60563 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60568 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60561 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,23 | −39,13 | x | ||
MN18729 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN18789 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60559 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60560 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
LBCE13942 | W. cerradensis | Left | Ceará | 47 | Russas | CE | −4,93 | −37,97 | mt-Cytb; i7Fgb | PP953679; PP953718 | |
LBCE10412 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953672; PP953723 | |
LBCE5255 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953670; PP953707 | |
MN1531 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1532 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1764 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN60657 | W. cerradensis | Left | Ceará | 50 | Guaraciaba do Norte | CE | −41,67 | −40,75 | x | ||
MN18737 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18738 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18739 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60569 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60654 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18544 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18546 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18548 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18549 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18550 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18551 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18552 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18553 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18554 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18555 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18556 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18557 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18558 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18559 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18560 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18561 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18562 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18563 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18564 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18669 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18670 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18671 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18672 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18673 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18674 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18676 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18677 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18678 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18680 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18681 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18741 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18800 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18802 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18803 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18805 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18806 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN27213 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
UNB2594 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953721 |
UNB2595 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953722 |
MN71267 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,89 | x | ||
MRT3874 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,60 | −47,89 | mt-Cytb; IRBP | PP953685; PP953664 | |
CRB2716 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953689 | |
CRB2718 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb; i7Fgb | PP953686; PP953724 | |
CRB2729 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953688 | |
MN81688 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN81694 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN4169 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN4170 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN67022 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | i7Fgb | PP953726 |
MN67023 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1614 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1617 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB2064 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1776 | W. cerradensis | Left | Jaborandi | 63 | Formoso | MG | −14,95 | −46,23 | x | ||
MN61657 | W. cerradensis | Left | Jaborandi | 63 | Jaborandi | BA | −13,62 | −44,44 | i7Fgb | PP953720 | |
MN83081 | W. cerradensis | Left | Maranhão | 56 | Mirador | MA | −6,36 | −44,35 | x | i7Fgb | PP953728 |
LEM63 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953681; PP953719 | |
LEM75 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953683; PP953727 | |
MN18491 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18589 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18590 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18684 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18742 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18743 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18744 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18746 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18796 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18798 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18799 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18591 | W. cerradensis | Left | Pesqueira | 36 | Belo Jardim | PE | −8,33 | −36,42 | x | ||
MN18613 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18675 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18679 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18682 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
UNB2706 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
UNB2715 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
MN75110 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75111 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75126 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
MN75144 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
CIT1708 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953674; PP953739; PP953649 | |
MZUSP30453/UUPI174 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953687; PP953742; PP953652 | |
MUFAL0249/MJJS414 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | ||
MUFAL0250/MJJS415 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | mt-Cytb; i7Fgb; IRBP | PP953669; PP953744; PP953643 | |
MUFAL0255/MJJS431 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | mt-Cytb; i7Fgb; IRBP | PP953682; PP953740; PP953653 |
MUFAL0179/ALN294 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; IRBP | PP953666; PP953656 | |
MUFAL0180/ALN295 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | x | mt-Cytb; IRBP | PP953676; PP953651 |
MUFAL0184/ALN299 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953675; PP953734; PP953657 | |
MUFAL0190/ALN305 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953667; PP953736; PP953663 | |
MUFAL0195/ALN310 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953671; PP953738; PP953650 | |
MUFAL0199/ALN314 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953673; PP953743; PP953658 | |
MUFAL0182/ALN297 | W. cerradensis | Left | Piranhas | 27 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953668; PP953735; PP953654 | |
UNB2762 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
UNB2763 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
MUFAL0286/MJJS489 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; IRBP | PP953684; PP953655 | |
MUFAL0287/MJJS490 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; i7Fgb; IRBP | PP953680; PP953737; PP953662 | |
MN18776 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18778 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18779 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18780 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18781 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18782 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18783 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18784 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18785 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18786 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18787 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18493 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18593 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18598 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18599 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18688 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18689 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN17382 | W. cerradensis | Left | Quebrangulo | 31 | Palmeira dos Índios | AL | −9,40 | −36,70 | x | ||
MN18788 | W. cerradensis | Left | Quebrangulo | 32 | Limoeiro de Anadia | AL | −9,73 | −36,50 | x | ||
MN18594 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18690 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18767 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18768 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18769 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18771 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18773 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18811 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x |
Reg. number . | Species . | SF riverside . | OTU . | Gazetteer . | Locality . | State . | Lat100 . | Long100 . | Morphological data . | Genetic data . | GenBank number . |
---|---|---|---|---|---|---|---|---|---|---|---|
JBC16 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953694; PP953717 | |
JBC18 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953690; PP953725 | |
JBC26 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953693; PP953715 | |
MCN-M1968 | W. pyrrhorhinos | Right | Berilo | 2 | Leme do Prado | MG | −17,08 | −42,69 | x | ||
MCN-M1507 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M1700 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2013 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2262 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73314 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73416 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73419 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73431 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73435 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73437 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73438 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73442 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73453 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73461 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73477 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73520 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN−M1053 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MCN−M1054 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MN68601 | W. pyrrhorhinos | Right | Caetité | 10 | Piripá | BA | −14,93 | −41,72 | x | ||
MN18441 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18442 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18725 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18726 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18727 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18756 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18758 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60780 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60783 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60784 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN63357 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | i7Fgb | PP953713 |
MN63420 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | mt-Cytb; i7Fgb | PP953695; PP953709 |
MN18527 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18528 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18529 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18530 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18531 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18532 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18698 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18699 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18700 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18701 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MN18702 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MTR2980 | W. pyrrhorhinos | Right | Caetité | 15 | Santo Inácio | BA | −11,10 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953698; PP953731; PP953648 | |
UFPB9790 | W. pyrrhorhinos | Right | Canindé de São Francisco | 21 | Nossa Senhora da Glória | SE | −10,21 | −37,42 | mt-Cytb; i7Fgb | PP953705; PP953714 | |
UFPB9780 | W. pyrrhorhinos | Right | Canindé de São Francisco | 22 | Monte Alegre de Sergipe | SE | −10,03 | −37,56 | mt-Cytb; i7Fgb | PP953702; PP953716 | |
MUFAL0265/MJJS459 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; i7Fgb; IRBP | PP953704; PP953732; PP953646 | |
UFPB9764/ARB788 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | mt-Cytb | PP953706 |
UNB2761 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2764 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2801 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
CIT1017 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953699; PP953730; PP953661 | |
CIT959 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; IRBP | PP953700; PP953644 | |
CIT961 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953691; PP953733; PP953645 | |
LBCE5202 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb | PP953701; PP953710 | |
MUFAL0283/MJJS486 | W. pyrrhorhinos | Right | Canindé de São Francisco | 25 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; IRBP | PP953703, PP953647 | |
MN76145 | W. pyrrhorhinos | Right | Berilo | 5 | Juramento | BA | −16,85 | −43,58 | x | mt-Cytb | PP953696 |
MCN-M2182 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,91 | −42,60 | x | ||
MCN-M1511 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2459 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2893 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2902 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2945 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2952 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M1052 | W. pyrrhorhinos | Right | Berilo | 7 | Grao Mogol | MG | −16,56 | −42,89 | x | ||
MCN-M2699 | W. pyrrhorhinos | Right | Berilo | 8 | Porteirinha | MG | −15,74 | −43,03 | x | ||
MN34412 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN34413 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62180 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62181 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN18751 | W. pyrrhorhinos | Right | Morro do Chapéu | 16 | Palmeiras | BA | −12,52 | −41,55 | x | ||
MN18428 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18498 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18502 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18503 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18506 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18508 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18509 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18510 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18511 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18512 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18513 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18516 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18517 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18521 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18522 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18523 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18525 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60772 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60778 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN71607 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapeu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953697; PP953712 |
MN71608 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapéu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953692; PP953711 |
MN18715 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18716 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18717 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18718 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18719 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18720 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18723 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18760 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18761 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18762 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18763 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18764 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18765 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60791 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60792 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60793 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN11661 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18445 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18752 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18753 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18754 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18755 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN60789 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18454 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18457 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18459 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18460 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18461 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18463 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18466 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18468 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18469 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18470 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18474 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18475 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18476 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18477 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18480 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18481 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18482 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18483 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18484 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18485 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18486 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18622 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18624 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
MN18656 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
UFPB4043 | W. cerradensis | Left | Caruaru | 39 | Bezerros | PE | −9,17 | −37,37 | mt-Cytb; i7Fgb | PP953678, PP953708 | |
CIT1680/SA01 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953665; PP953659; PP953729 | |
CIT1681/SA02 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953677; PP953741; 953,660 | |
MN18586 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18587 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18588 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18745 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18747 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41412 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN25456 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41413 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN60756 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60757 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60761 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60763 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18451 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18496 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18592 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60752 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60753 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60754 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
UNB2710 | W. cerradensis | Left | Ceará | 43 | Jardim | CE | −7,58 | −39,30 | x | ||
MN18790 | W. cerradensis | Left | Ceará | 44 | Crato | CE | −8,23 | −39,67 | x | ||
MN17449 | W. cerradensis | Left | Ceará | 45 | Missao Velha | CE | −7,23 | −39,13 | x | ||
MN18808 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60563 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60568 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60561 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,23 | −39,13 | x | ||
MN18729 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN18789 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60559 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60560 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
LBCE13942 | W. cerradensis | Left | Ceará | 47 | Russas | CE | −4,93 | −37,97 | mt-Cytb; i7Fgb | PP953679; PP953718 | |
LBCE10412 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953672; PP953723 | |
LBCE5255 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953670; PP953707 | |
MN1531 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1532 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1764 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN60657 | W. cerradensis | Left | Ceará | 50 | Guaraciaba do Norte | CE | −41,67 | −40,75 | x | ||
MN18737 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18738 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18739 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60569 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60654 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18544 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18546 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18548 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18549 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18550 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18551 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18552 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18553 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18554 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18555 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18556 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18557 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18558 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18559 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18560 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18561 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18562 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18563 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18564 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18669 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18670 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18671 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18672 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18673 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18674 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18676 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18677 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18678 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18680 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18681 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18741 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18800 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18802 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18803 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18805 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18806 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN27213 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
UNB2594 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953721 |
UNB2595 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953722 |
MN71267 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,89 | x | ||
MRT3874 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,60 | −47,89 | mt-Cytb; IRBP | PP953685; PP953664 | |
CRB2716 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953689 | |
CRB2718 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb; i7Fgb | PP953686; PP953724 | |
CRB2729 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953688 | |
MN81688 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN81694 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN4169 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN4170 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN67022 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | i7Fgb | PP953726 |
MN67023 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1614 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1617 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB2064 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1776 | W. cerradensis | Left | Jaborandi | 63 | Formoso | MG | −14,95 | −46,23 | x | ||
MN61657 | W. cerradensis | Left | Jaborandi | 63 | Jaborandi | BA | −13,62 | −44,44 | i7Fgb | PP953720 | |
MN83081 | W. cerradensis | Left | Maranhão | 56 | Mirador | MA | −6,36 | −44,35 | x | i7Fgb | PP953728 |
LEM63 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953681; PP953719 | |
LEM75 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953683; PP953727 | |
MN18491 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18589 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18590 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18684 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18742 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18743 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18744 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18746 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18796 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18798 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18799 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18591 | W. cerradensis | Left | Pesqueira | 36 | Belo Jardim | PE | −8,33 | −36,42 | x | ||
MN18613 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18675 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18679 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18682 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
UNB2706 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
UNB2715 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
MN75110 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75111 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75126 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
MN75144 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
CIT1708 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953674; PP953739; PP953649 | |
MZUSP30453/UUPI174 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953687; PP953742; PP953652 | |
MUFAL0249/MJJS414 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | ||
MUFAL0250/MJJS415 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | mt-Cytb; i7Fgb; IRBP | PP953669; PP953744; PP953643 | |
MUFAL0255/MJJS431 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | mt-Cytb; i7Fgb; IRBP | PP953682; PP953740; PP953653 |
MUFAL0179/ALN294 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; IRBP | PP953666; PP953656 | |
MUFAL0180/ALN295 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | x | mt-Cytb; IRBP | PP953676; PP953651 |
MUFAL0184/ALN299 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953675; PP953734; PP953657 | |
MUFAL0190/ALN305 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953667; PP953736; PP953663 | |
MUFAL0195/ALN310 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953671; PP953738; PP953650 | |
MUFAL0199/ALN314 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953673; PP953743; PP953658 | |
MUFAL0182/ALN297 | W. cerradensis | Left | Piranhas | 27 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953668; PP953735; PP953654 | |
UNB2762 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
UNB2763 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
MUFAL0286/MJJS489 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; IRBP | PP953684; PP953655 | |
MUFAL0287/MJJS490 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; i7Fgb; IRBP | PP953680; PP953737; PP953662 | |
MN18776 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18778 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18779 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18780 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18781 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18782 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18783 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18784 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18785 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18786 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18787 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18493 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18593 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18598 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18599 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18688 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18689 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN17382 | W. cerradensis | Left | Quebrangulo | 31 | Palmeira dos Índios | AL | −9,40 | −36,70 | x | ||
MN18788 | W. cerradensis | Left | Quebrangulo | 32 | Limoeiro de Anadia | AL | −9,73 | −36,50 | x | ||
MN18594 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18690 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18767 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18768 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18769 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18771 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18773 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18811 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x |
Reg. number . | Species . | SF riverside . | OTU . | Gazetteer . | Locality . | State . | Lat100 . | Long100 . | Morphological data . | Genetic data . | GenBank number . |
---|---|---|---|---|---|---|---|---|---|---|---|
JBC16 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953694; PP953717 | |
JBC18 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953690; PP953725 | |
JBC26 | W. pyrrhorhinos | Right | Berilo | 1 | Jenipapo de Minas | MG | −17,08 | −42,26 | mt-Cytb; i7Fgb | PP953693; PP953715 | |
MCN-M1968 | W. pyrrhorhinos | Right | Berilo | 2 | Leme do Prado | MG | −17,08 | −42,69 | x | ||
MCN-M1507 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M1700 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2013 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN-M2262 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73314 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73416 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73419 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73431 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73435 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73437 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73438 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73442 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73453 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73461 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73477 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MN73520 | W. pyrrhorhinos | Right | Berilo | 3 | Berilo | MG | −16,95 | −42,45 | x | ||
MCN−M1053 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MCN−M1054 | W. pyrrhorhinos | Right | Berilo | 4 | Araçuaí | MG | −16,81 | −41,98 | x | ||
MN68601 | W. pyrrhorhinos | Right | Caetité | 10 | Piripá | BA | −14,93 | −41,72 | x | ||
MN18441 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18442 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18725 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18726 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18727 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18756 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN18758 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60780 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60783 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN60784 | W. pyrrhorhinos | Right | Caetité | 11 | Vitoria da Conquista | BA | −14,85 | −40,83 | x | ||
MN63357 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | i7Fgb | PP953713 |
MN63420 | W. pyrrhorhinos | Right | Caetité | 12 | Caetité | BA | −14,07 | −42,47 | x | mt-Cytb; i7Fgb | PP953695; PP953709 |
MN18527 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18528 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18529 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18530 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18531 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18532 | W. pyrrhorhinos | Right | Caetité | 13 | Jequié | BA | −13,85 | −40,08 | x | ||
MN18698 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18699 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18700 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −39,97 | −39,97 | x | ||
MN18701 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MN18702 | W. pyrrhorhinos | Right | Caetité | 14 | Jaguaquara | BA | −13,52 | −39,97 | x | ||
MTR2980 | W. pyrrhorhinos | Right | Caetité | 15 | Santo Inácio | BA | −11,10 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953698; PP953731; PP953648 | |
UFPB9790 | W. pyrrhorhinos | Right | Canindé de São Francisco | 21 | Nossa Senhora da Glória | SE | −10,21 | −37,42 | mt-Cytb; i7Fgb | PP953705; PP953714 | |
UFPB9780 | W. pyrrhorhinos | Right | Canindé de São Francisco | 22 | Monte Alegre de Sergipe | SE | −10,03 | −37,56 | mt-Cytb; i7Fgb | PP953702; PP953716 | |
MUFAL0265/MJJS459 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; i7Fgb; IRBP | PP953704; PP953732; PP953646 | |
UFPB9764/ARB788 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | mt-Cytb | PP953706 |
UNB2761 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2764 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
UNB2801 | W. pyrrhorhinos | Right | Canindé de São Francisco | 23 | Caninde de São Francisco | SE | −9,64 | −37,79 | x | ||
CIT1017 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953699; PP953730; PP953661 | |
CIT959 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; IRBP | PP953700; PP953644 | |
CIT961 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb; IRBP | PP953691; PP953733; PP953645 | |
LBCE5202 | W. pyrrhorhinos | Right | Canindé de São Francisco | 24 | Curaçá | BA | −8,98 | −39,90 | mt-Cytb; i7Fgb | PP953701; PP953710 | |
MUFAL0283/MJJS486 | W. pyrrhorhinos | Right | Canindé de São Francisco | 25 | Caninde de São Francisco | SE | −9,64 | −37,79 | mt-Cytb; IRBP | PP953703, PP953647 | |
MN76145 | W. pyrrhorhinos | Right | Berilo | 5 | Juramento | BA | −16,85 | −43,58 | x | mt-Cytb | PP953696 |
MCN-M2182 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,91 | −42,60 | x | ||
MCN-M1511 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2459 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2893 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2902 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2945 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M2952 | W. pyrrhorhinos | Right | Berilo | 6 | Jose Goncalves de Minas | MG | −16,74 | −42,65 | x | ||
MCN-M1052 | W. pyrrhorhinos | Right | Berilo | 7 | Grao Mogol | MG | −16,56 | −42,89 | x | ||
MCN-M2699 | W. pyrrhorhinos | Right | Berilo | 8 | Porteirinha | MG | −15,74 | −43,03 | x | ||
MN34412 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN34413 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62180 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN62181 | W. pyrrhorhinos | Right | Berilo | 9 | Jaíba | MG | −15,33 | −43,67 | x | ||
MN18751 | W. pyrrhorhinos | Right | Morro do Chapéu | 16 | Palmeiras | BA | −12,52 | −41,55 | x | ||
MN18428 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18498 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18502 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18503 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18506 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18508 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18509 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18510 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18511 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18512 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18513 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18516 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18517 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18521 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18522 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18523 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN18525 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60772 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN60778 | W. pyrrhorhinos | Right | Morro do Chapéu | 17 | Seabra | BA | −12,42 | −41,77 | x | ||
MN71607 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapeu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953697; PP953712 |
MN71608 | W. pyrrhorhinos | Right | Morro do Chapéu | 18 | Morro do Chapéu | BA | −11,55 | −41,16 | x | mt-Cytb; i7Fgb | PP953692; PP953711 |
MN18715 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18716 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18717 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18718 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18719 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18720 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18723 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18760 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18761 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18762 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18763 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18764 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18765 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60791 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60792 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN60793 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN11661 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18722 | W. pyrrhorhinos | Right | Morro do Chapéu | 19 | Feira de Santana | BA | −12,27 | −38,97 | x | ||
MN18445 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18752 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18753 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18754 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18755 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN60789 | W. pyrrhorhinos | Right | Serrinha | 20 | Serrinha | BA | −11,65 | −39,00 | x | ||
MN18454 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18457 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18459 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18460 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18461 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18463 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18466 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18468 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18469 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18470 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18474 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18475 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18476 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18477 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18480 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18481 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18482 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18483 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18484 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18485 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18486 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18622 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −8,28 | −35,97 | x | ||
MN18624 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
MN18656 | W. cerradensis | Left | Caruaru | 38 | Caruaru | PE | −7,28 | −35,97 | x | ||
UFPB4043 | W. cerradensis | Left | Caruaru | 39 | Bezerros | PE | −9,17 | −37,37 | mt-Cytb; i7Fgb | PP953678, PP953708 | |
CIT1680/SA01 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953665; PP953659; PP953729 | |
CIT1681/SA02 | W. cerradensis | Left | Caruaru | 40 | Sítio Alfredo | PE | −7,85 | −35,58 | mt-Cytb; i7Fgb; IRBP | PP953677; PP953741; 953,660 | |
MN18586 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18587 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18588 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18745 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN18747 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41412 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN25456 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN41413 | W. cerradensis | Left | Ceará | 41 | Triunfo | PE | −7,83 | −38,10 | x | ||
MN60756 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60757 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60761 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60763 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18451 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18496 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN18592 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60752 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60753 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
MN60754 | W. cerradensis | Left | Ceará | 42 | Bodocó | PE | −7,77 | −36,93 | x | ||
UNB2710 | W. cerradensis | Left | Ceará | 43 | Jardim | CE | −7,58 | −39,30 | x | ||
MN18790 | W. cerradensis | Left | Ceará | 44 | Crato | CE | −8,23 | −39,67 | x | ||
MN17449 | W. cerradensis | Left | Ceará | 45 | Missao Velha | CE | −7,23 | −39,13 | x | ||
MN18808 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60563 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60568 | W. cerradensis | Left | Ceará | 45 | Missão Velha | CE | −7,23 | −39,13 | x | ||
MN60561 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,23 | −39,13 | x | ||
MN18729 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN18789 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60559 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
MN60560 | W. cerradensis | Left | Ceará | 46 | Campos Sales | CE | −7,07 | −40,37 | x | ||
LBCE13942 | W. cerradensis | Left | Ceará | 47 | Russas | CE | −4,93 | −37,97 | mt-Cytb; i7Fgb | PP953679; PP953718 | |
LBCE10412 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953672; PP953723 | |
LBCE5255 | W. cerradensis | Left | Ceará | 48 | Jaguaruana | CE | −4,82 | −37,77 | mt-Cytb; i7Fgb | PP953670; PP953707 | |
MN1531 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1532 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN1764 | W. cerradensis | Left | Ceará | 49 | Monte Alegre | CE | −4,35 | −39,30 | x | ||
MN60657 | W. cerradensis | Left | Ceará | 50 | Guaraciaba do Norte | CE | −41,67 | −40,75 | x | ||
MN18737 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18738 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18739 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60569 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN60654 | W. cerradensis | Left | Ceará | 51 | São Benedito | CE | −4,04 | −40,88 | x | ||
MN18544 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18546 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18548 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18549 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18550 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18551 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18552 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18553 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18554 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18555 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18556 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18557 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18558 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18559 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18560 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18561 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18562 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18563 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18564 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18669 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18670 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18671 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18672 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18673 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18674 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18676 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18677 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18678 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18680 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18681 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18741 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18800 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18802 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18803 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18805 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN18806 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
MN27213 | W. cerradensis | Left | Garanhuns | 33 | Garanhuns | PE | −8,88 | −36,48 | x | ||
UNB2594 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953721 |
UNB2595 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,88 | x | i7Fgb | PP953722 |
MN71267 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,62 | −47,89 | x | ||
MRT3874 | W. cerradensis | Left | Jaborandi | 57 | Paranã | TO | −12,60 | −47,89 | mt-Cytb; IRBP | PP953685; PP953664 | |
CRB2716 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953689 | |
CRB2718 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb; i7Fgb | PP953686; PP953724 | |
CRB2729 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | mt-Cytb | PP953688 | |
MN81688 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN81694 | W. cerradensis | Left | Jaborandi | 58 | Correntina | BA | −13,34 | −44,64 | x | ||
MN4169 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN4170 | W. cerradensis | Left | Jaborandi | 59 | Barreiras | BA | −12,15 | −44,59 | x | ||
MN67022 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | i7Fgb | PP953726 |
MN67023 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1614 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1617 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB2064 | W. cerradensis | Left | Jaborandi | 62 | Jaborandi | BA | −13,62 | −44,44 | x | ||
UNB1776 | W. cerradensis | Left | Jaborandi | 63 | Formoso | MG | −14,95 | −46,23 | x | ||
MN61657 | W. cerradensis | Left | Jaborandi | 63 | Jaborandi | BA | −13,62 | −44,44 | i7Fgb | PP953720 | |
MN83081 | W. cerradensis | Left | Maranhão | 56 | Mirador | MA | −6,36 | −44,35 | x | i7Fgb | PP953728 |
LEM63 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953681; PP953719 | |
LEM75 | W. cerradensis | Left | Pesqueira | 34 | Buíque | PE | −8,51 | −37,28 | mt-Cytb; i7Fgb | PP953683; PP953727 | |
MN18491 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18589 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18590 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18684 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18742 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18743 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18744 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18746 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18796 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18798 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18799 | W. cerradensis | Left | Pesqueira | 35 | Pesqueira | PE | −8,35 | −36,68 | x | ||
MN18591 | W. cerradensis | Left | Pesqueira | 36 | Belo Jardim | PE | −8,33 | −36,42 | x | ||
MN18613 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18675 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18679 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
MN18682 | W. cerradensis | Left | Pesqueira | 37 | São Bento de Una | PE | −8,47 | −36,33 | x | ||
UNB2706 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
UNB2715 | W. cerradensis | Left | Piauí | 52 | Sao João do Piaui | PI | −8,36 | −42,25 | x | ||
MN75110 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75111 | W. cerradensis | Left | Piauí | 53 | Canto do Buriti | PI | −8,10 | −42,93 | x | ||
MN75126 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
MN75144 | W. cerradensis | Left | Piauí | 54 | Eliseu Martins | PI | −8,08 | −43,65 | x | ||
CIT1708 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953674; PP953739; PP953649 | |
MZUSP30453/UUPI174 | W. cerradensis | Left | Piauí | 55 | Uruçui-Una | PI | −886667,00 | −44,97 | mt-Cytb; i7Fgb; IRBP | PP953687; PP953742; PP953652 | |
MUFAL0249/MJJS414 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | ||
MUFAL0250/MJJS415 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | mt-Cytb; i7Fgb; IRBP | PP953669; PP953744; PP953643 | |
MUFAL0255/MJJS431 | W. cerradensis | Left | Piranhas | 25 | Piranhas | AL | −9,62 | −37,76 | x | mt-Cytb; i7Fgb; IRBP | PP953682; PP953740; PP953653 |
MUFAL0179/ALN294 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; IRBP | PP953666; PP953656 | |
MUFAL0180/ALN295 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | x | mt-Cytb; IRBP | PP953676; PP953651 |
MUFAL0184/ALN299 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953675; PP953734; PP953657 | |
MUFAL0190/ALN305 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953667; PP953736; PP953663 | |
MUFAL0195/ALN310 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953671; PP953738; PP953650 | |
MUFAL0199/ALN314 | W. cerradensis | Left | Piranhas | 26 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953673; PP953743; PP953658 | |
MUFAL0182/ALN297 | W. cerradensis | Left | Piranhas | 27 | Delmiro Golveia | AL | −9,38 | −37,98 | mt-Cytb; i7Fgb; IRBP | PP953668; PP953735; PP953654 | |
UNB2762 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
UNB2763 | W. cerradensis | Left | Piranhas | 27 | Olho d’Agua do Casado | AL | −9,54 | −37,29 | x | ||
MUFAL0286/MJJS489 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; IRBP | PP953684; PP953655 | |
MUFAL0287/MJJS490 | W. cerradensis | Left | Piranhas | 28 | Inhapi | AL | −9,22 | −37,75 | mt-Cytb; i7Fgb; IRBP | PP953680; PP953737; PP953662 | |
MN18776 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18778 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18779 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18780 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18781 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18782 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18783 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18784 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18785 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18786 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18787 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18493 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18593 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18598 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18599 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18688 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN18689 | W. cerradensis | Left | Quebrangulo | 30 | Quebrangulo | AL | −9,32 | −36,47 | x | ||
MN17382 | W. cerradensis | Left | Quebrangulo | 31 | Palmeira dos Índios | AL | −9,40 | −36,70 | x | ||
MN18788 | W. cerradensis | Left | Quebrangulo | 32 | Limoeiro de Anadia | AL | −9,73 | −36,50 | x | ||
MN18594 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18690 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18767 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18768 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18769 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18771 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18773 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x | ||
MN18811 | W. cerradensis | Left | Santana do Ipanema | 29 | Santana do Ipanema | AL | −9,37 | −37,23 | x |
Author notes
Camilla B Di-Nizo, Ana Lazar and Carlos A Cunha-Filho contributed equally to the manuscript.