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Occurrence of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in the state of Maranhão, Brazil

Abstract

The bat genus Sturnira is widely distributed in the Neotropical region, from northwestern Mexico to northern Argentina, and four species occur in Brazil: Sturnira lilium, Sturnira giannae, Sturnira magna, and Sturnira tildae. The present study is the first to record Sturnira tildae in the state of Maranhão, Brazil, based on morphological and molecular diagnoses. The specimen was identified based on its cranial and morphometric traits. The diagnostic traits include discreetly bilobed inner upper incisors with a broad base, lower first and second molars with lingual cusps separated by shallow grooves, and forearm longer than 45 mm. The molecular sequences of Cytochrome C Oxidase Subunit 1 (COI) and 16S rRNA genes confirmed the morphological identification and thus the occurrence of Sturnira tildae in the Amazon biome of Maranhão. This record represents an eastward extension of the known distribution of the species in the Amazonia, to Cândido Mendes, Maranhão, within an area dominated by dense rainforest and influenced by tides.

Keywords.
16S rRNA; Amazon; COI; DNA barcode; Range extension; Stenodermatinae

INTRODUCTION

Brazil has is the country with the third richest bat fauna in the world, with 181 species (including eight endemics) representing 68 genera and nine families (Garbino et al., 2020Garbino, G.S.T.; Gregorin, R.; Lima, I.P.; Loureiro, L.; Moras, L.M.; Moratelli, R.; Nogueira, M.R.; Pavan, A.C.; Tavares & Peracchi, V.C. 2020. Updated checklist of Brazilian bats: versão 2020. Comitê da Lista de Morcegos do Brasil - CLMB. Sociedade Brasileira para o Estudo de Quirópteros (SBEQ). Available: Available: https://www.sbeq.net/lista-de-especies . Access: 01/05/2021.
https://www.sbeq.net/lista-de-especies...
; Velazco 2021Velazco, P.M. 2021. Murciélagos del Perú/Bats of Peru. Available: Available: http://www.paulvelazco.com/murcielagos_peru.html . Access: 10/07/2021.
http://www.paulvelazco.com/murcielagos_p...
). Much of this diversity is found in the Amazon biome, which is home to most of the species known to occur in Brazil (Bernard et al., 2011Bernard, E.; Tavares, V.C. & Sampaio, E. 2011. Compilação atualizada das espécies de morcegos (Chiroptera) para a Amazônia Brasileira. Biota Neotropica, 11(1): 35-46. http://doi.org/10.1590/S1676-06032011000100003
http://doi.org/10.1590/S1676-06032011000...
). In this scenario, the Amazon of Maranhão, in the eastern extreme of the biome, is one of the Amazonian regions that have a fragmented distribution of bat species records, but which are gradually a number of recent studies have provided important insights into the distribution of chiropterans in this region (Bernard et al., 2011Bernard, E.; Tavares, V.C. & Sampaio, E. 2011. Compilação atualizada das espécies de morcegos (Chiroptera) para a Amazônia Brasileira. Biota Neotropica, 11(1): 35-46. http://doi.org/10.1590/S1676-06032011000100003
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; Oliveira et al., 2011Oliveira, T.G.; Júnior, J.S.S. & Dias, P.A. 2011. Mamíferos da Amazônia maranhense. In: Martins, M.B. & Oliveira, T.G. (Eds.). Amazônia Maranhense: Diversidade e conservação. Belém, Museu Paraense Emílio Goeldi. p. 251-267.; Olímpio et al., 2016Olímpio, A.P.M.; Ventura, M.C.S.; Mascarenhas, M.J.O.; Nascimento, D.C.; Andrade, F.A.G.; Fraga, E.C. & Barros, M.C. 2016. Bat fauna of the Cerrado savanna of eastern Maranhão, Brazil, with new species occurrences. Biota Neotropica, 16(3), e20150089. http://doi.org/10.1590/1676-0611-BN-2015-0089
http://doi.org/10.1590/1676-0611-BN-2015...
; Lima et al., 2018Lima, A.C.S.; Cardoso, F.H.S.; Mendes, S.B.; Fraga, E.C. & Barros, M.C. 2018. New records of Niceforo’s big-eared bat, Trinycteris nicefori (Sanborn, 1949) (Chiroptera, Phyllostomidae), from the state of Maranhão, Brazil. ZooKeys, 787: 127-134. http://doi.org/10.3897/zookeys.787.26538
http://doi.org/10.3897/zookeys.787.26538...
; Olímpio et al., 2018Olímpio, A.P.M.; Cardoso, F.H.S.; Costa, C.L.S.; Fraga, E.C. & Barros, M.C. 2018. Expansion of the known range of the lesser bulldog bat, Noctilio albiventris Desmarest, 1818 (Chiroptera, Noctilionidae) in the Brazilian Cerrado. Check List, 14(2): 313-317. http://doi.org/10.15560/14.2.313
http://doi.org/10.15560/14.2.313...
; Mendes et al., 2020Mendes, S.B.; Lima, A.C.S.; Reis, T.S.; Fraga, E.C. & Barros, M.C. 2020. First record of Cynomops planirostris (Peters, 1865) (Chiroptera, Molossidae) from Maranhão state, Brazil, based on morphological and molecular data. Brazilian Journal of Biology, 80(2): 405-409. http://doi.org/10.1590/1519-6984.213968
http://doi.org/10.1590/1519-6984.213968...
).

Bats of the family Phyllostomidae are the most ecologically diverse group of mammals, and the second most speciose mammalian family, with 216 recognized species (Taylor & Tuttle, 2019Taylor, M. & Tuttle, M.D. 2019. BATS: an illustrated guide to all species. (4ª ed.), China: science editor & photographer, 403pp.). In recent years, a number of studies reporting the fauna of poorly-known areas associated with phylogenetic analyses, have advanced the scientific understanding of phyllostomid diversity, including the discovery of new species and the expansion of the inventories available for many genera, such as Sturnira (Miretzki et al., 2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.).

The phyllostomid genus Sturnira has a wide distribution in the Neotropical region, occurring from Mexico to northern Argentina (Gardner, 2008Gardner, A.L. 2008. Tribe Sturnirini. In: Gardner, A.L. (Ed.). Mammals of South America. Volume 1: Marsupials, Xenarthrans, Shrews, and Bats. Chicago, The University of Chicago Press. p. 363-376.). Sturnira is the most speciose phyllostomid genus, with 23 recognized species (Fleming et al., 2020Fleming, T.H.; Dávalos, L.M. & Mello, M.A.R. 2020. Phyllostomid bats: a unique mammalian radiation. Chicago, The University of Chicago Press. 489p.), of which, four occur in Brazil - Sturnira lilium (Geoffroy, 1810), Sturnira giannaeVelazco & Patterson, 2019Velazco, P.M. & Patterson, B.D. 2019. Small mammals of the Mayo river basin in northern Peru, with the description of a new species of Sturnira (Chiroptera: Phyllostomidae). Bulletin of the American Museum of Natural History, 429: 1-67., Sturnira magna De La Torre, 1966 and Sturnira tildaeDe La Torre, 1959De La Torre, L. 1959. A new species of bat of the genus Sturnira (Phyllostomidae) from the Island of Trinidad, West Indies. Natural History Miscellanea, Chicago, 166: 1-6. (Garbino et al., 2020Garbino, G.S.T.; Gregorin, R.; Lima, I.P.; Loureiro, L.; Moras, L.M.; Moratelli, R.; Nogueira, M.R.; Pavan, A.C.; Tavares & Peracchi, V.C. 2020. Updated checklist of Brazilian bats: versão 2020. Comitê da Lista de Morcegos do Brasil - CLMB. Sociedade Brasileira para o Estudo de Quirópteros (SBEQ). Available: Available: https://www.sbeq.net/lista-de-especies . Access: 01/05/2021.
https://www.sbeq.net/lista-de-especies...
). Sturnira tilde is found in Brazil, Colombia, Ecuador, the Guianas, Peru, Bolivia, Trinidad and Tobago, and Venezuela (Simmons, 2005Simmons, N.B. 2005. Order Chiroptera. In: Wilson, D.E. & Reeder, D.M. (Eds.). Mammals species of the world: a taxonomic a geographic reference. 3. ed. Baltimore, Johns Hopkins University Press. v. 1, p. 312-529.; Gardner, 2008Gardner, A.L. 2008. Tribe Sturnirini. In: Gardner, A.L. (Ed.). Mammals of South America. Volume 1: Marsupials, Xenarthrans, Shrews, and Bats. Chicago, The University of Chicago Press. p. 363-376.). In Brazil, this species has been recorded in the states of Amapá, Amazonas, Pará, Acre, Tocantins, Ceará, Pernambuco, Bahia, Mato Grosso, Goiás, Mato Grosso do Sul, Espirito Santo, Rio de Janeiro, São Paulo, Paraná, and Santa Catarina (Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
).

Relatively few data are available on the diet or reproductive patterns of S. tildae, but this bat is assumed to be an important seed disperser, which contributes to the regeneration of forested areas (Simmons, 2005Simmons, N.B. 2005. Order Chiroptera. In: Wilson, D.E. & Reeder, D.M. (Eds.). Mammals species of the world: a taxonomic a geographic reference. 3. ed. Baltimore, Johns Hopkins University Press. v. 1, p. 312-529.; Gardner, 2008Gardner, A.L. 2008. Tribe Sturnirini. In: Gardner, A.L. (Ed.). Mammals of South America. Volume 1: Marsupials, Xenarthrans, Shrews, and Bats. Chicago, The University of Chicago Press. p. 363-376.). S. tildae shares a number of external characteristics with the other members of the genus, such as the lack of a tail, narrow and hairy interfemoral membrane, small ears, a small, broad nasal leaf, and posterior members and feet hairy, as far as the claws (Peracchi et al., 2011Peracchi, A.L.; Lima, I.P.; Reis, N.R.; Nogueira, M.R. & Filho, H.O. 2011. Ordem Chiroptera. In: Reis, N.R.; Peracchi, A.L.; Pedro, W.A. & Lima, I.P. Mamíferos do Brasil. 2. ed. Londrina. p. 155-234.). The color of the pelage varies from tones of yellow to brown, with some males having tufts of orangish or dark reddish-brown hair on the shoulders (Reis et al., 2017Reis, N.R.; Peracchi, A.L.; Batista, C.B.; Lima, I.P. & Pereira, A.D. 2017. História natural dos morcegos brasileiros: chave de identificação de espécies. Rio de Janeiro, Technical Books. 416p.).

The external measurements of S. tildae are similar to S. lilium, although S. lilium tends to be smaller (Gardner, 2008Gardner, A.L. 2008. Tribe Sturnirini. In: Gardner, A.L. (Ed.). Mammals of South America. Volume 1: Marsupials, Xenarthrans, Shrews, and Bats. Chicago, The University of Chicago Press. p. 363-376.). Some studies point to the possibility of identification errors of identification related to the morphological similarities of these species and the overlap in their geographic distributions (Miretzki et al., 2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.; Sampaio et al., 2016Sampaio, E.; Lim, B. & Peters, S, 2016. Sturnira tildae. The IUCN Red List of Threatened Species 2016: e.T20960A22050501. http://doi.org/10.2305/IUCN.UK.2016-2.RLTS.T20960A22050501.en
http://doi.org/10.2305/IUCN.UK.2016-2.RL...
; Velazco & Patterson, 2017Velazco, P. & Patterson, B.D. 2017. Sturnira lilium. The IUCN Red List of Threatened Species 2017: e.T88159688A22049384. http://doi.org/10.2305/IUCN.UK.2017-2.RLTS.T88159688A22049384.en
http://doi.org/10.2305/IUCN.UK.2017-2.RL...
; Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
). In areas that are in sympatry, S. lilium differs from S. tildae only by dental and morphometric characteristics (Simmons & Voss, 1988Simmons, N.B. & Voss, R.S. 1998. The mammals of Paracou, French Guiana: a neotropical lowland rainforest fauna. Part I. Bats. Bulletin of the American Museum of Natural History, 237: 1-219.; Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
). The present study uses morphological and molecular data to report on a new record of S. tildae from the state of Maranhão, which extends the known geographic distribution of the species in Brazil.

MATERIAL AND METHODS

Bats were collected in June 2016 in a fragment of forest located within the Amazon biome of the Brazilian state of Maranhão, in the municipality of Cândido Mendes. Specimen collection followed the procotol of Pacheco (2004Pacheco, S.M. 2004. Técnicas de campo empregadas no estudo de quirópteros. Caderno La Salle XI, Canoa, 1(2): 195-202.) and permits were duly provided by the Brazilian federal agency for the environment (IBAMA/SISBIO permit number 42670-3). The vegetation of the study region is dense rainforest typical of the Amazon biome, and it has a humid equatorial climate, as well as being influenced by the tides of the Maracaçumé River, which crosses the town of Cândido Mendes (Bandeira, 2013Bandeira, I.C.N. 2013. Geodiversidade do estado do Maranhão. Programa Geologia do Brasil. Levantamento da Geodiversidade. Teresina, CPRM. 294p.).

The specimen described here was collected using a 3 m high and 12 m long mist-net, with a 25 mm mesh. The age of the specimen was determined in the field based on the ossification of the phalangeal epiphyses, and its sex and reproductive status were also recorded (Brunet & Austad, 2004Brunet, A.K. & Austad, S.N. 2004. Aging studies on bats: a review. Biogerontology, 5(4): 211-222. http://doi.org/10.1023/B:BGEN.0000038022.65024.d8
http://doi.org/10.1023/B:BGEN.0000038022...
). The specimen was photographed, euthanized, labeled, and stored on ice for transportation to the Genetics and Molecular Biology Laboratory (GENBIMOL) of Universidade Estadual do Maranhão (UEMA) in Caxias, Maranhão, where it was weighed and measured, and a sample of a muscle tissue was extracted, which was stored in ethanol 70° for the molecular analyses.

The skull was extracted through the buccal aperture. Once clean, the skull was clarified with 10% peroxide and dried in a stove at 30ºC, after which, it was labeled and stored in a clean recipient. The specimen was fixed in formaldehyde and preserved in ethanol at UEMA’s Laboratory of Genetics and Molecular Biology, on the campus of Caxias, and then transferred to the mammal collection of the Federal University of Paraíba, in João Pessoa, Brazil, where is it deposited. The specimen was identified based on its external traits and craniometric measurements, following Vizzoto & Taddei (1973Vizzoto, L.D. & Taddei, V.A. 1973. Chave para determinação de quirópteros brasileiros. Revista da Faculdade de Filosofia, Ciências e Letras. Boletim de Ciências, São José do Rio Preto, 1: 1-72.), Simmons & Voss (1998Simmons, N.B. & Voss, R.S. 1998. The mammals of Paracou, French Guiana: a neotropical lowland rainforest fauna. Part I. Bats. Bulletin of the American Museum of Natural History, 237: 1-219.), and Reis et al. (2013Reis, N.R.; Fregonezi, M.N.; Peracchi, A.L. & Shibatta, A.O. 2013. Morcegos do Brasil: guia de campo. Rio de Janeiro, Technical Books. 225p., 2017Reis, N.R.; Peracchi, A.L.; Batista, C.B.; Lima, I.P. & Pereira, A.D. 2017. História natural dos morcegos brasileiros: chave de identificação de espécies. Rio de Janeiro, Technical Books. 416p.). Measurements taken include the length of right and left forearms, ear, tragus, foot, greatest length of the skull, basal length and condylobasal length, width of the brain case and the mastoid, zygomatic width, the length of the upper tooth row, and the width across the molars (Table 1). Body mass, after the specimen had been dead for hours, was determined using a precision balance after euthanasia of the specimen.

Table 1
Craniometric measurements (in mm) of the Sturnira tildae specimen from Cândido Mendes, Maranhão, Brazil (present study), together with the values recorded from specimens of the same species from Recife (Pernambuco), Morretes (Paraná), and French Guiana.

The total DNA was extracted from the muscle tissue using Promega’s Wizard Genomic DNA Purification kit, following the default protocol. Two mitochondrial genes, Cytochrome C Oxidase Subunit 1 (COI) and rRNA 16S, were amplified by Polymerase Chain Reaction (PCR) using the primers LCO-1490 and HCO-2198 for the COI gene (Folmer et al., 1994Folmer, O.; Black, M.; Hoeh, W.; Lutz, R. & Vrijenhoek, R. 1994. DNA primers for amplification of mitochondrial Cytochrome C Oxidase Subunit 1 from diverse metazoan invertebrates. Molecular Marine Biology and Biotechnology, 3(5): 294-299.) and L1987 and H2609 for the rRNA 16S (Palumbi et al., 2002Palumbi, S.; Martin, A.; Romano, S.; McMillan, W.O.; Stice, L.; Grabowski, G. & MacMillan, W.O. 2002. The simple fool’s guide to PCR, version 2.0. University of Hawaii, Honolulu.). The samples were sequenced by the dideoxyterminal method of Sanger et al. (1977Sanger, F.; Nichlen, S. & Coulson, A.R. 1977. DNA sequencing with chain termination inhibitors. Proceedings of the National Academy of Sciences Cambridge, 74(12): 5463-5467.) in an ABI Prism™ 3500 (Applied Biosystems, USA) automatic DNA sequencer, using the Big Dye kit. The sequences were edited and aligned in BIOEDIT 7.0 (Hall, 1999Hall, T.A. 1999. BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic acids symposium, 41: 95-98.), with the genetic divergence matrices being complied in MEGA X (Kumar et al., 2018Kumar, S.; Stecher, G.; Lim, Knyaz & Tamura, K. 2018. MEGA X: Molecular Evolutionary Genetics Analysis across computing platforms. Molecular Biology and Evolution, 35(6): 1547-1549.) using the Kimura 2-parameter algorithm. The sequences were plotted in the BOLD Systems v4 (www.boldsystems.org) and BLAST (https://blast.ncbi.nlm.nih.gov/Blast.cgi) platforms to confirm their identification and determine their degree of similarity with sequences of other Sturnira species.

RESULTS

We collected an adult female S. tildae (field number: RRM 117, voucher: UFPB 11757) in June 2016 from a farm located within the urban perimeter of the town of Cândido Mendes (01°27′21″S, 45°43′32″W), in the Amazon biome, within an area containing remnants of rainforest. The length of the right forearm was 45.77 mm, while its left forearm was 46.34 mm. The length of ear of the specimen was 12.95 mm, the tragus 5.46 mm, and the foot 12.45 mm. The specimen was a non-lactating which had ectoparasites, orange-brown pelage, with the venter paler than the dorsum, and dark hairs around the eyes (Fig. 1).

Figure 1
Sturnira tildae (female, RRM 117) collected em Cândido Mendes, in the Amazon biome of Maranhão state, Brazil.

Sturnira tildae was also identified based on the following set of morphological cranial traits: small brain case and broad, high rostrum, slightly bilobed upper incisors with a wide base and narrower points, and first and second lower molars with lingual cusps separated by shallow grooves with no vertical border (Fig. 2A-D and Table 1).

Figure 2
Skull of Sturnira tildae (RRM 117). (A) dorsal view showing the small braincase; (B) lateral view showing the broad, elongated rostrum; (C) lateral view of the mandible showing the first and second molars with lingual cusps separated by shallow grooves; (D) frontal view of the upper incisors, showing the slightly bilobed internal incisors with a wide base. Scale bar: 5 mm. Source: Olímpio, A.P.M.; Lima, A.C.S.

The present study provides the first record of S. tildae from the Brazilian state of Maranhão, and only the fifth for the Brazilian Northeast geographic region (two from Bahia state - Faria & Baumgarten, 2007Faria, D. & Baumgarten, J. 2007. Shade cacao plantations (Theobroma cacao) and bat conservation in southern Bahia, Brazil. Biodiversity and Conservation, 16(2): 291-312. http://doi.org/10.1007/s10531-005-8346-5
http://doi.org/10.1007/s10531-005-8346-5...
; Faria, 2006Faria, D. 2006. Phyllostomid bats of a fragmented landscape in the north-eastern Atlantic forest, Brazil. Journal of Tropical Ecology, 22(5): 531-542. http://doi.org/10.1017/S0266467406003385
http://doi.org/10.1017/S0266467406003385...
, one from Pernambuco; Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
and one from Ceará - Novaes & Laurindo, 2014Novaes, R.L.M. & Laurindo, R.S. 2014. Morcegos da Chapada do Araripe, Nordeste do Brasil. Papéis Avulsos de Zoologia, 54(22): 1-13. http://doi.org/10.1590/0031-1049.2014.54.22
http://doi.org/10.1590/0031-1049.2014.54...
). The geographically closest locality to Cândido Mendes with records of S. tildae is Santa Barbara, in the neighboring state of Pará, which is ca. 280 km due west (Fonseca, 2006Fonseca, R.T.D. 2006. Diversidade da quiropterofauna (Mammalia) no Parque Ecológico de Gunma, Santa Bárbara do Pará. Master thesis. Belém, Universidade Federal do Pará. 120p.). There is also a record from the municipality of Muaná, in Pará (Marques-Aguiar et al., 2002Marques-Aguiar, S.A.; Melo, C.C.S.; Aguiar, G.F.S. & Queiroz, J.A.L. 2002. Levantamento preliminar da mastofauna da região de Anajás-Muaná, Ilha de Marajó, Pará, Brasil. Revista Brasileira de Zoologia, 19(3): 841-854. http://doi.org/10.1590/S0101-81752002000300022
http://doi.org/10.1590/S0101-81752002000...
), which is 402 km west of Cândido Mendes. Both these localities are within the Amazon biome. South of Maranhão, the nearest locality is in the municipality of Goiatins, in Tocantins state (Maas et al., 2018Maas, A.C.S.; Gomes, L.; Martins, M.A.; Dias, D.; Pol, A.; Chaves, G.F.; Schutte, M.; Araújo, R. & Peracchi, A.L. 2018. Bats in a Cerrado landscape of Northern Brazil: species occurrence, influence of environmental heterogeneity and seasonality, and eight new records for the state of Tocantins. Mammalia, 82(5): 469-480. http://doi.org/10.1515/mammalia-2017-0023
http://doi.org/10.1515/mammalia-2017-002...
), which is 724 km to the south, in the Cerrado savanna biome, while the nearest record to the east is from the municipality of Barbalha, in Ceará state, at a distance of 967 km, in the Caatinga biome (Novaes & Laurindo, 2014Novaes, R.L.M. & Laurindo, R.S. 2014. Morcegos da Chapada do Araripe, Nordeste do Brasil. Papéis Avulsos de Zoologia, 54(22): 1-13. http://doi.org/10.1590/0031-1049.2014.54.22
http://doi.org/10.1590/0031-1049.2014.54...
) (Fig. 3). The present study extends the known distribution of S. tildae to the eastern extreme of the Amazon biome.

Figure 3
Geographic distribution of Sturnira tildae in Brazil. The locality reported in the present study in the state of Maranhão is shown by a star. The Brazilian biomes are shaded in black (Pantanal), darker to lighter gray (Pampas, Atlantic Forest, Cerrado, and Caatinga, in this order), and white (Amazon). Source: adapted from Martins et al. (2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
).

The sequence of the rRNA 16S gene obtained from the specimen analyzed in the present study diverged by 0.4% from those of S. tildae from French Guiana and by 4.8% from S. lilium. The BLAST search identified a genetic similarity of 100% with S. tildae from French Guiana. In the case of the COI gene sequences, intraspecific genetic divergence between the study specimen and sequences from French Guiana, Surinam, Ecuador, and Guyana was 0.92-1.58%, while it was 11.8% in relation to S. lilium. In the BOLD Systems platform, the sequence returned a similarity of 99.09% with S. tildae from French Guiana (Table 2). These results are consistent with the morphological and craniometric identification of the specimen, and confirm the occurrence of S. tildae in the Amazon biome of Maranhão state.

Table 2
Interspecific genetic divergence in Sturnira tildae based on the sequences of the COI gene, using the 2-parameter Kimura algorithm. Lophostoma silvicola and Carollia perspicillata were included as outgroups. Legend: GUY = Guyana, SUR = Suriname, ECU = Ecuador, FGU = French Guiana, CM = Candido Mendes, CX = Caxias (Maranhão).

DISCUSSION

In the present study, the cranial and morphological measurements of the specimen, are typical of S. tildae, as defined by De La Torre (1959De La Torre, L. 1959. A new species of bat of the genus Sturnira (Phyllostomidae) from the Island of Trinidad, West Indies. Natural History Miscellanea, Chicago, 166: 1-6.), Simmons & Voss (1998Simmons, N.B. & Voss, R.S. 1998. The mammals of Paracou, French Guiana: a neotropical lowland rainforest fauna. Part I. Bats. Bulletin of the American Museum of Natural History, 237: 1-219.), Miretzki et al. (2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.), López-Baucells et al. (2016López-Baucells, A.; Rocha, R.; Bobrowiec, P.E.D.; Palmeirim, J.M. & Meyer, C.F.J. 2016. Field guide to amazonian bats. Manaus, Editora INPA. 173p.), Velazco & Patterson (2019Velazco, P.M. & Patterson, B.D. 2019. Small mammals of the Mayo river basin in northern Peru, with the description of a new species of Sturnira (Chiroptera: Phyllostomidae). Bulletin of the American Museum of Natural History, 429: 1-67.), and Martins et al. (2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
). The cranial and dental measurements of the specimen (skull, basal, and condylobasal lengths, the length of the upper tooth row, and the postorbital and zygomatic widths, the width of the braincase, and the width across the molars) are all very similar to those of the S. tildae specimens collected in Recife, Pernambuco (Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
) and Morretes, Paraná (Miretzki et al., 2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.). This indicates that differences due to the geographic or sexual variation are negligible.

The species S. tildae has great morphological similarities with S. lilium, making identification difficult. (Simmons & Voss, 1998Simmons, N.B. & Voss, R.S. 1998. The mammals of Paracou, French Guiana: a neotropical lowland rainforest fauna. Part I. Bats. Bulletin of the American Museum of Natural History, 237: 1-219.). A number of diagnostic traits can nevertheless be used to distinguished the two taxa, including the length of the forearm, which exceeds 45 mm in S. tildae, but never exceeds this value in S. lilium (Simmons & Voss, 1998Simmons, N.B. & Voss, R.S. 1998. The mammals of Paracou, French Guiana: a neotropical lowland rainforest fauna. Part I. Bats. Bulletin of the American Museum of Natural History, 237: 1-219.; Reis et al., 2013Reis, N.R.; Fregonezi, M.N.; Peracchi, A.L. & Shibatta, A.O. 2013. Morcegos do Brasil: guia de campo. Rio de Janeiro, Technical Books. 225p., 2017Reis, N.R.; Peracchi, A.L.; Batista, C.B.; Lima, I.P. & Pereira, A.D. 2017. História natural dos morcegos brasileiros: chave de identificação de espécies. Rio de Janeiro, Technical Books. 416p.; Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
); the lighter coloration of the pelage of the venter in S. tildae in comparison with S. lilium, and the larger lengths of the ear, tibia, wing, and condylobasal length in S. tildae (Fazzolari-Correa, 1995Fazzolari-Correa, S. 1995. Aspectos sistemáticos, ecológicos e reprodutivos de morcegos na Mata Atlântica. Doctoral thesis. São Paulo, Universidade de São Paulo, Instituto de Biociências. 168p.; Davis, 1980Davis, W.B. 1980. New Sturnira (Chiroptera, Phylostomidae) from Central and South America, with key to currently recognized species. Occasional Papers of the Museum of Texas Tech University, 93: 1-16. http://doi.org/10.5962/bhl.title.156537
http://doi.org/10.5962/bhl.title.156537...
). All these differences were also observed in the S. tildae specimen analyzed in the present study.

The dentition provides the most reliable evidence for the differentiation of the two species, given the presence of bilobed internal superior incisives and wider in S. tildae, than observed in S. lilium (Eisenberg, 1989Eisenberg, J.F. 1989. Mammals of the Neotropics: the northern Neotropics. Chicago, The University of Chicago Press. v. 1, 449p.), as well as the lingual cusps of the first and second molars of the mandible, S. lilium has high lingual cusps, separated by a deep vertical notch between the first and second molars and in S. tildae these cusps are low and separated by shallow notches (Miretzki et al., 2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.). These authors considered the differences in the configuration of the cusps of the mandibular molars to be completely reliable for the distinction of the specimens of S. lilium and S. tildae from Paracou, in French Guiana, and this conclusion was further confirmed in the present study.

The analyses of the 16S rRNA and COI genes revealed a high degree of similarity, in both cases, between the specimen presented here and S. tildae from French Guiana, with a genetic divergence of less than 2% in comparison with the specimens from of different localities, which is consistent with the 2% intraspecific threshold of the COI marker established for bats by Clare et al. (2011Clare, E.L.; Lim, B.K.; Fenton, M.B. & Hebert, P.D.N. 2011. Neotropical bats: estimating species diversity with DNA barcodes. PLoS ONE, 6(7): 322-648. http://doi.org/10.1371/journal.pone.0022648
http://doi.org/10.1371/journal.pone.0022...
). Despite the fact that S. lilium and S. tildae present major morphological similarities, the analysis of the rRNA 16S sequences indicated a divergence of 4.8% between the S. tildae specimen presented here and S. lilium, increasing to 11.8% for the COI gene. The genetic data thus support conclusively the morphological and craniometric analyses, and confirm the occurrence of S. tildae in Maranhão.

As for distribution, S. tildae is considered a common species within its geographic distribution (Wilson 1996Wilson, D.E. 1996. Neotropical bats: a checklist with conservatian status. In: Gibson, A.C.; Mildred, E. & Mathias, B.G. Neotropical Biodiversity and Conservation, University of Califonia, Los Angeles, Califonia, pp. 167-177.; Miretzki et al., 2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.), with a distinct preference for more humid forest environments (Trajano, 1984Trajano, E. 1994. Ecologia de populações de morcegos cavernícolas em uma região cárstica do sudeste do brasil. Revista Brasileira de Zoologia, 2(5): 255-320. http://doi.org/10.1590/S0101-81751984000100001
http://doi.org/10.1590/S0101-81751984000...
; Marques, 1985Marques, S.A. 1985. Novos registros de morcegos do Parque Nacional da Amazônia (Tapajós), com observações do período de atividade noturna e reprodução. Boletim do Museu Paraense Emílio Goeldi Zoologia, 2(1): 71-83. Available: https://repositorio.museu-goeldi.br/handle/mgoeldi/401.
https://repositorio.museu-goeldi.br/hand...
; Brosset et al., 1996Brosset, A.; Charles-Oominique, P.; Cockle, A.; Cosson, J.F. & Masson, O. 1996. Bat communities and dcforestation in French Guiana. Canadian Journal of Zoology, 74(11): 1974-1982. http://doi.org/10.1139/z96-224
http://doi.org/10.1139/z96-224...
; Simmons & Voss, 1998Simmons, N.B. & Voss, R.S. 1998. The mammals of Paracou, French Guiana: a neotropical lowland rainforest fauna. Part I. Bats. Bulletin of the American Museum of Natural History, 237: 1-219.; Miretzki et al., 2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.; Novaes & Laurindo, 2014Novaes, R.L.M. & Laurindo, R.S. 2014. Morcegos da Chapada do Araripe, Nordeste do Brasil. Papéis Avulsos de Zoologia, 54(22): 1-13. http://doi.org/10.1590/0031-1049.2014.54.22
http://doi.org/10.1590/0031-1049.2014.54...
), such as the locality surveyed during the present study. Even so, S. tildae has been captured relatively infrequently in most bat field studies, in all different biomes (Oliveira, 2000Oliveira, E.R. 2000. Espaço ecomorfológico da fauna de quirópteros da região do Alto Tocantins, GO: uma perspectiva através da análise da morfologia alar. Master thesis. Rio de Janeiro, Universidade Federal do Rio de Janeiro. 82p.; Marques-Aguiar et al., 2002Marques-Aguiar, S.A.; Melo, C.C.S.; Aguiar, G.F.S. & Queiroz, J.A.L. 2002. Levantamento preliminar da mastofauna da região de Anajás-Muaná, Ilha de Marajó, Pará, Brasil. Revista Brasileira de Zoologia, 19(3): 841-854. http://doi.org/10.1590/S0101-81752002000300022
http://doi.org/10.1590/S0101-81752002000...
; Miretzki et al., 2002Miretzki, M.; Perrachi, A.L. & Bianconi, G.V. 2002. Southernmost records of Sturnira tildae De La Torre, 1959 (Chiroptera: Phyllostomidae) in Brazil. Mammalia, 66(2): 306-309.; Carvalho et al., 2013Carvalho, F.; Fabián, M.E. & Menegheti, J.O. 2013. Vertical structure of an assemblage of bats (Mammalia: Chiroptera) in a fragment of Atlantic Forest in Southern Brazil. Zoologia, 30(5): 491-498. http://doi.org/10.1590/S1984-46702013000500004
http://doi.org/10.1590/S1984-46702013000...
; Luz et al., 2013Luz, J.L.; Costa, L.M.; Jordão-Nogueira, T.; Esbérard, C.E.L. & Bergallo, H.G. 2013. Morcegos em área de Floresta Montana, Visconde de Mauá, Resende, Rio de Janeiro. Biota Neotropica, 13(2): 190-195. http://doi.org/10.1590/S1676-6032013000200018
http://doi.org/10.1590/S1676-60320130002...
; Menezes et al., 2015Menezes, L.F.; Pinto, A.C.D.C.; Contildes, M.D.R. & Peracchi, A.L. 2015. Lista de morcegos (Mammalia Chiroptera) do Parque Natural Municipal da Serra do Mendanha, Município do Rio de Janeiro, RJ, Brasil. In: Pontes, J.A.L. (Ed.). Biodiversidade carioca. Rio de Janeiro, Technical Books. p. 238-245.; Maas et al., 2018Maas, A.C.S.; Gomes, L.; Martins, M.A.; Dias, D.; Pol, A.; Chaves, G.F.; Schutte, M.; Araújo, R. & Peracchi, A.L. 2018. Bats in a Cerrado landscape of Northern Brazil: species occurrence, influence of environmental heterogeneity and seasonality, and eight new records for the state of Tocantins. Mammalia, 82(5): 469-480. http://doi.org/10.1515/mammalia-2017-0023
http://doi.org/10.1515/mammalia-2017-002...
; Cláudio et al., 2020Cláudio, V.C.; Barbosa, G.P.; Rocha, V.J.; Moratelli, R. & Rassy, F.B. 2020. The bat fauna (Mammalia: Chiroptera) of Carlos Botelho State Park, Atlantic Forest of Southeastern Brazil, including new distribution records for the state of São Paulo. Zoologia, 37(e36514): 1-32. http://doi.org/10.3897/zoologia.37.e36514
http://doi.org/10.3897/zoologia.37.e3651...
; Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
).

In Brazil, S. tildae has been recorded in the Amazon, Atlantic Forest, Cerrado, and Caatinga biomes. In the Amazon biome (IBGE, 2019Instituto Brasileiro de Geografia e Estatística (IBGE). 2019. Biomas e sistema costeiro-marinho do Brasil: compatível com a escala 1:250.000. Rio de Janeiro. Coordenação de Recursos Naturais e Estudos Ambientais, Relatórios metodológicos (IBGE), ISSN 0101-2843, 164pp.), there are records from the Brazilian states of Amazonas, Acre, Rondônia, Pará, Amapá, Roraima, and Mato Grosso (Tavares et al., 2008Tavares, V.C.; Gregorin, R. & Peracchi, A.L. 2008. Diversidade de morcegos no Brasil: lista atualizada com comentários sobre distribuição e taxonomia. In: Pacheco, S.M.; Marques, R.V. & Esberard, C.E.L. (Eds.). Morcegos no Brasil: Biologia, Sistemática, Ecologia e Conservação. Armazém Digital Comunicação Ltda., Porto Alegre, 25-58.; Reis et al., 2013Reis, N.R.; Fregonezi, M.N.; Peracchi, A.L. & Shibatta, A.O. 2013. Morcegos do Brasil: guia de campo. Rio de Janeiro, Technical Books. 225p.; Novaes & Laurindo, 2014Novaes, R.L.M. & Laurindo, R.S. 2014. Morcegos da Chapada do Araripe, Nordeste do Brasil. Papéis Avulsos de Zoologia, 54(22): 1-13. http://doi.org/10.1590/0031-1049.2014.54.22
http://doi.org/10.1590/0031-1049.2014.54...
; Reis et al., 2017Reis, N.R.; Peracchi, A.L.; Batista, C.B.; Lima, I.P. & Pereira, A.D. 2017. História natural dos morcegos brasileiros: chave de identificação de espécies. Rio de Janeiro, Technical Books. 416p.), and the closest locality to the present study site is 280 km west, in Pará. This is the fifth record of the occurrence of S. tildae in the Brazilian Northeast. The previous records included one from the Caatinga biome, in Barbalha, Ceará state (Novaes & Laurindo, 2014Novaes, R.L.M. & Laurindo, R.S. 2014. Morcegos da Chapada do Araripe, Nordeste do Brasil. Papéis Avulsos de Zoologia, 54(22): 1-13. http://doi.org/10.1590/0031-1049.2014.54.22
http://doi.org/10.1590/0031-1049.2014.54...
), and three from the Atlantic Forest, in Ilhéus (Faria & Baumgarten, 2007Faria, D. & Baumgarten, J. 2007. Shade cacao plantations (Theobroma cacao) and bat conservation in southern Bahia, Brazil. Biodiversity and Conservation, 16(2): 291-312. http://doi.org/10.1007/s10531-005-8346-5
http://doi.org/10.1007/s10531-005-8346-5...
) and Una (Faria, 2006Faria, D. 2006. Phyllostomid bats of a fragmented landscape in the north-eastern Atlantic forest, Brazil. Journal of Tropical Ecology, 22(5): 531-542. http://doi.org/10.1017/S0266467406003385
http://doi.org/10.1017/S0266467406003385...
), both in Bahia, and Recife in Pernambuco state (Martins et al., 2020Martins, T.C.S.L.; Leal, E.S.B.; Neves, C.H.C.B.; Ferreira, A.F.; Silva, L.G.; Garcia, A.C.L. & Montes, M.A. 2020. First record of Sturnira tildae De La Torre, 1859 (Chiroptera, Phyllostomidae) for the state of Pernambuco, Brazil. Oecologia Australis, 24(1): 223-234. http://doi.org/10.4257/oeco.2020.2401.22
http://doi.org/10.4257/oeco.2020.2401.22...
). Barbalha is very close - about 20 km - to Floresta Nacional do Araripe. The area is considered to be a relict of Atlantic Forest in the middle of the Caatinga (Silveira et al., 2019Silveira, M.H.B.; Mascarenhas, R.; Cardoso, D. & Batalha-Filho, H. 2019. Pleistocene climatic instability drove the historical distribution of forest islands in the northeastern Brazilian Atlantic Forest. Palaeogeography, Paleoclimatology, Palaeoecology, 527: 67-76.).

CONCLUSIONS

The present study recorded the occurrence of S. tildae in the Amazon biome of the Brazilian state of Maranhão, based on both morphological and molecular evidence. This is the first record of the species for the state, and the fifth for the Brazilian Northeast, and extends the known distribution of the species to the municipality of Cândido Mendes, 280 km east of the nearest locality in the Amazon biome. The findings of the study reinforce the need for attention when identifying the species of the genus Sturnira, in particular in areas where S. lilium and S. tildae are likely to be captured together and then released, given that the considerable morphological similarities of these sympatric taxa may result in errors of identification. As S. tildae occurs more frequently in moist forests, new records are expected in other Amazonian areas in Maranhão, as well as in Brejos de Altitude habitats within the Caatinga biome (see Tabarelli & Santos, 2004Tabarelli, M. & Santos, A.M.M. 2004. Uma Breve Descrição Sobre a História Natural dos Brejos Nordestinos. In: Pôrto, K.C.; Cabral, J.J.P. & Tabarelli, M. (Eds.). Brejos de Altitude em Pernambuco e Paraíba - História Natural, Ecologia e Conservação. 17-24pp.).

ACKNOWLEDGMENTS

ACSL and FHSC were supported by postgraduate fellowships and BATPC was supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) postdoctoral fellowships. CLSC was supported by a postgraduate grant from the Universidade Estadual do Maranhão (UEMA). This study was financed in part by CAPES - Financial Code 001 and the Foundation for Research and Scientific and Technological Development of Maranhão (FAPEMA).

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  • Published with the financial support of the "Programa de Apoio às Publicações Científicas Periódicas da USP"

Edited by

Edited by: Luís Fábio Silveira

Publication Dates

  • Publication in this collection
    04 Oct 2021
  • Date of issue
    2021

History

  • Received
    28 June 2021
  • Accepted
    22 July 2021
  • Published
    16 Aug 2021
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