Hostname: page-component-78c5997874-s2hrs Total loading time: 0 Render date: 2024-11-14T04:44:33.323Z Has data issue: false hasContentIssue false

First report of a morulated Ascaridoidea (Nematoda) egg in an avian coprolite from the Paleogene of the Paraíba Valley, State of São Paulo, Brazil

Published online by Cambridge University Press:  11 November 2024

G. Macêdo do Carmo*
Affiliation:
Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Presidente Antônio Carlos Ave., 31270-901, Belo Horizonte, Brazil
A. Hadassa da Silva Guilherme Luiz
Affiliation:
Universidade Federal de Juiz de Fora, Instituto de Ciências Biológicas, José Lourenço Kelmer Str., 36036-900, Juiz de Fora, Brazil
J.F. Passos
Affiliation:
Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Presidente Antônio Carlos Ave., 31270-901, Belo Horizonte, Brazil
S. de Souza Lima
Affiliation:
Universidade Federal de Juiz de Fora, Instituto de Ciências Biológicas, José Lourenço Kelmer Str., 36036-900, Juiz de Fora, Brazil
Hermínio I. de Araújo-Júnior
Affiliation:
Universidade do Estado do Rio de Janeiro, Faculdade de Geologia, São Francisco Xavier Str., 20550-013, Rio de Janeiro, Brazil
F.B. Pereira
Affiliation:
Universidade Federal de Minas Gerais, Instituto de Ciências Biológicas, Presidente Antônio Carlos Ave., 31270-901, Belo Horizonte, Brazil.
*
Corresponding author: G. Macêdo do Carmo; Email: gugaatwts@hotmail.com
Rights & Permissions [Opens in a new window]

Abstract

Ascaridoidea (Nematoda) is a widespread superfamily of nematodes that comprises gastrointestinal parasites from all major groups of vertebrates. Although this taxon probably emerged in the Carboniferous, its Brazilian fossil record includes mostly eggs, found in ancient remains, collected in paleontological and archeological sites from the Mesozoic and Cenozoic Eras. The Tremembé Formation (Oligocene of the Taubaté Basin) has become an important source for paleoparasitological studies in avian coprolites during the third decade of the 21st century, with reports of eggs only at only a single cell stage, of embryonic development. Here we present the first egg of Ascaridoidea preserved containing morula, from a bird coprolite recovered from the shales of the Tremembé Formation. Three coprolites, from the outcrop of Aligra Comércio de Argila S/A, Taubaté municipality (State of São Paulo), were rehydrated and subjected to spontaneous sedimentation. Based on morphological and morphometric features and diet and zoopaleontological context, the trace fossils were assigned to piscivorous birds. The egg found showed morphological characteristics typical of Ascaridoidea: namely spherical form, ornamented, and somewhat thick shell. Moreover, this superfamily includes several taxa that infect piscivorous birds and fish in heteroxenous life cycles and produce eggs with similar features as the egg found in the present study. The paleoparasitological information associated with the paleofaunistic diversity of birds and fish from the Tremembé Formation, reveal that the ancient Brazilian paleoenvironments provided subsidies for the rise and success of nematodes infecting these animals during the Paleogene.

Type
Short Communication
Copyright
© The Author(s), 2024. Published by Cambridge University Press

Introduction

Ascaridoidea (sensu Hodda, Reference Hodda2022) is a widespread superfamily of nematodes comprising gastrointestinal parasites infecting mammals, including humans, birds, reptiles, amphibians, and fish (Hartwich, Reference Hartwich, Anderson, Chabaud and Willmott2009). This taxon probably emerged in the Carboniferous parasitizing terrestrial tetrapods and, subsequently, moving to aquatic environments and infecting other hosts like bony and cartilaginous fishes (Li et al., Reference Li, lü, Nadler, Gibson, Zhang, Chen, Zhao and Guo2018).

The Brazilian fossil record related to ascaridoids includes mostly eggs found in ancient remains collected in paleontological and archeological sites and, even though the egg morphology is rather uniform and unspecific, some species have been proposed based on these immature forms. For example Ascarites rufferi, was described from an egg found in a coprolite of Cynodontia, the taxonomic bridge between reptiles and mammals, which was recovered in the Santa Maria Formation, Paraná Basin, Brazil (Silva et al., Reference Silva, Borba, Dutra, Leles, Da-Rosa, Ferreira and Araujo2014). Bauruascaris cretacicus and B. adamantinensis were proposed based on eggs found in coprolites of Crocodilomorpha from the Adamantina Formation (Bauru Group, Brazil) (Cardia et al., Reference Cardia, Bertini, Camossi and Letizio2018; Reference Cardia, Bertini, Camossi and Letizio2019). In addition, Poinar & Boucot (Reference Poinar and and Boucot2006) described the species A. priscus and A. gerus from eggs in a single dinosaur coprolite. Ascaridoid parasitic forms have been more frequently reported in Cenozoic ancient remains dated from the Holocene (Gonçalves et al., Reference Gonçalves, Araújo and Ferreira2003; Leles et al., Reference Leles, Araújo, Ferreira, Vicente and Iñiguez2008; Camacho et al., Reference Camacho, Pessanha, Leles, Dutra, Silva, Souza and Araujo2013; Jaeger et al., Reference Jaeger, Taglioretti, Dias and Iñiguez2013a, Reference Jaeger, Taglioretti, Fugassa, Dias, Neto and Iñiguez2013b; Sianto et al., Reference Sianto, Souza, Chame, Luz, Guidon, Pessis and Araújo2014; Guedes et al., Reference Guedes, Borba, Camacho, Neto, Dias and Iñiguez2020; Iñiguez et al., Reference Iñiguez, Brito, Guedes and Chaves2022).

The Tremembé Formation (Oligocene of the Taubaté Basin), aged between 33.9 and 23.03 million years ago, is an intercalation between shale and clay layers with lacustrine origin, and it has become an important source for paleoparasitological studies in avian coprolites, providing different well-preserved morphotypes of helminth eggs, protozoan cysts, and non-sporulated oocysts (Carmo et al., Reference Carmo, Garcia, Vieira, Lima, Araújo-Júnior and Pinheiro2023; Carmo et al., Reference Carmo, Berto, Pereira, Lima, Araújo-Júnior and Pinheiro2024a). Currently, the helminth eggs from this geological unit have been reported only at a single cell stage of embryonic development (Carmo et al., Reference Carmo, Garcia, Vieira, Lima, Araújo-Júnior and Pinheiro2023). Here, we report the first egg of Ascaridoidea preserved containing morula, from a single bird coprolite recovered from the Paraíba Valley, as well as discuss some insights into the potential of its lower taxon of origin.

Materials and methods

Three coprolites were recovered from sedimentary rocks of the Tremembé Formation, Taubaté Basin, in 2023 at the outcrop of Aligra Comércio de Argila S/A, Taubaté municipality (State of São Paulo). Samples were rehydrated in 10 mL of 0.5% trisodium phosphate (Na3PO4) solution for 72 h (Callen, Reference Callen, Macneish and Byers1967; Fugassa et al., Reference Fugassa, Araújo and Guichón2006) and subjected to spontaneous sedimentation for 24 h (Hoffman et al., Reference Hoffman, Pons and Janer1934). A drop of sediment was placed on a glass slide, together with a drop of glycerine, covered with a coverslip (Ferreira et al., Reference Ferreira, Reinhard and Araújo2014), and observed using a light microscope Nikon Eclipse Ei with image capture system PrimeCam Intervision 12. A total of 20 slides were mounted for each sample of coprolite. Parasitological identification was performed based on morphology and morphometry (Ferreira et al., Reference Ferreira, Reinhard and Araújo2014); because there is no general literature for taxonomic identification of nematode eggs, the present identification was based on the expertise of the authors and comparisons with specific literature (see results and discussion for details). The avian origin of the coprolite was interpreted based on criteria adopted by Castro et al. (Reference Castro, Fernandes and Carvalho1988), Souto (Reference Souto2017), and Carmo et al. (Reference Carmo, Garcia, Vieira, Lima, Araújo-Júnior and Pinheiro2023). Two females of Contracaecum Railliet & Henry, 1912 (Ascaridoidea, Anisakidae) were collected from a single bird of the species Nannopterum brasilianum, and their uteri were dissected to obtain eggs that were used for comparison with the fossilized material. The genus Contracaecum was identified based on the following criteria: three well-developed labia, excretory pore at the base of subventral labium, presence of ventriculus with posterior appendix and intestinal caecum (Hartwich, Reference Hartwich, Anderson, Chabaud and Willmott2009; Gibbons, Reference Gibbons2010; Supplementary Figure S1). We also provided an micrography of an eimeriid oocyst (Fig. 1B), found by our research group in a previously analyzed sample, from the same geological formation, for comparisons.

Results and discussion

Coprolites were ovoid, grayish-yellow in colour, 10.80- to 28-mm long and 6.93- to 16.30-mm wide, containing fragmented remains of fishes (Fig. 1A). Based on morphological and morphometrical features, diet remains, and zoopaleontological context, the samples were assigned to piscivorous birds (Avialae, Neornithes). Some bird species may have benefited from periodic fish mortality because of seasonality (dry and wet seasons), which possibly supported the great success of this feeding habit in the Paraíba Valley during the Oligocene (Olson & Alvarenga, Reference Olson and Alvarenga2002).

Figure 1. Avian coprolite with fish bone fragments (A), eimeriid oocyst (B), Contracaecum egg (C), and fossilized egg of Ascaridoidea (C) from the Tremembé Formation, Taubaté Basin, State of São Paulo, Brazil.

A single slide from a single coprolite was positive for the parasite form, which was represented as a spherical egg, measuring 34.21 × 32.44 μm, containing morula, translucent, with somewhat thick and ornamented shell (Fig. 1D). The identification of immature parasitic forms (i.e., eggs and larvae), preserved without adult worms or genetic material, is rather difficult and generalist because these forms hold ancestral ontogenetic traces that are common within a higher taxa (i.e., family, order), show homogeneous morphology and lack specific traits (Carmo et al., Reference Carmo, Lima, Araújo-Júnior and Pereira2024b). Nevertheless, the egg exhibited morphological features typical of the Ascaridoidea nematodes (i.e., the shell with ornamentations [resembling a mammillated layer] and the pronounced spherical form). These characteristics are especially common in eggs from representatives of Ascarididae, Anisakidae, and Raphidascarididae, all belonging to Ascaridoidea (Koie & Fagerholm, Reference Koie and Fagerholm1995; Anderson, Reference Anderson2000; Carrera-Játiva et al., Reference Carrera-Játiva, Rodríguez-Hidalgo, Sevilla and Jiménez-Uzcátegui2014; Carvalho, Reference Carvalho, Santana, Gonçalves, Pinheiro and Giese2020).

The family Anisakidae was of particular interest in the present context because it includes some parasites that use piscivorous birds as definitive hosts and fish as intermediate or paratenic hosts, as well as produce eggs with similar morphometry and morphology as that found in the present study (Koie & Fagerholm, Reference Koie and Fagerholm1995; Anderson, Reference Anderson2000; Carrera-Játiva et al., Reference Carrera-Játiva, Rodríguez-Hidalgo, Sevilla and Jiménez-Uzcátegui2014; Carvalho, Reference Carvalho, Santana, Gonçalves, Pinheiro and Giese2020). The present egg was quite similar to those reported by Carrera-Játiva et al. (Reference Carrera-Játiva, Rodríguez-Hidalgo, Sevilla and Jiménez-Uzcátegui2014), and mainly to the morulated stages reported by Huizinga (Reference Huizinga1967), all assigned to the genus Contracaecum.

The Contracaecum eggs (54.36 – 61.27 × 43.82 – 50.04 μm; Fig. 1C) recovered from the dissected females were found in an initial stage of development, before morulation, similar to those reported by Huizinga (Reference Huizinga1967). Although the stages of development from these eggs were different, they showed morphological similarities such as an oval to spherical shape and an ornamented and relatively thinned shell that is typical from nematodes that have aquatic life cycles. Moreover, differences observed in the egg size between the fresh and the fossilized materials may be accounted for by intrinsic features of females from each species. According to Herreras et al. (Reference Herreras, Montero, Marcogliese, Raga and Balbuena2007), spatial constrictions imposed by uterine size may influence the number and size of eggs produced by females of anisakid nematodes.

Although the parasitic form reported here may have a size similar to that of some oocysts from Eimeriidae, previously found in the Tremembé Formation (Carmo et al., Reference Carmo, Berto, Pereira, Lima, Araújo-Júnior and Pinheiro2024a; Fig. 1B), it lacks common traits such as micropyle and micropyle cap. Moreover, we believe that the internal embryonic structure represents morula rather than developing sporocysts. In fact, more than 10 oocyst morphotypes were described in the Tremembé Formation, and none had preserved sporocysts or sporozoites (Carmo et al., Reference Carmo, Berto, Pereira, Lima, Araújo-Júnior and Pinheiro2024a). In this sense, sporocysts or sporozoites most likely degrade before feces fossilization in this paleoenvironment, or the abiotic conditions essential of sporulation (e.g., heat, humidity, oxygenation) were absent (Fayer, Reference Fayer1980; Berto et al., Reference Berto, Mcintosh and Lopes2014).

Fossilization is a singular phenomenon that takes place under specific conditions, which partially explains the lack of parasitological studies on material found in paleontological sites (Dentzien-Dias et al., Reference Dentzien-Dias, Poinar, Figueiredo, Pacheco, Horn and and Schultz2013; Carmo et al., Reference Carmo, Lima, Araújo-Júnior and Pereira2024b). Although we found only one egg in the present coprolites, the record of a morula reveals good potential for preservation of parasitic forms in the Tremembé Formation. In addition, the identification of the Ascaridoidea egg provides insights on the biogeographic distribution of this taxon, in the Brazilian territory, during the Oligocene.

The paleoparasitological information associated with the paleofaunistic diversity of birds and fishes from the Tremembé Formation (Carmo et al., Reference Carmo, Lima, Araújo-Júnior, Pinheiro, Melo and Couto-Ribeiro2024c) indicate that the ancient Brazilian paleoenvironments provided conditions for the rising and success of nematodes infecting such hosts during the Paleogene.

Previous paleoparasitological studies from the Tremembé Formation were performed in coprolites exclusively from the site Fazenda Santa Fé (Carmo et al., Reference Carmo, Garcia, Vieira, Lima, Araújo-Júnior and Pinheiro2023). Therefore, this is the first parasitological analysis in trace fossils from the outcrop of Aligra Comércio de Argila S/A, providing new perspectives related to the paleoparasitological studies in this lithostratigraphic unit, and expanding the knowledge on helminth infections in birds that inhabited the Paraiba Valley millions of years ago.

Supplementary material

The supplementary material for this article can be found at http://doi.org/10.1017/S0022149X24000610.

Conflict of interest

The authors declare no conflicts of interest.

Author contribution

G.M.d.C.: conceptualization, methodology, investigation, writing-original draft, writing-review & editing, funding acquisition. A.H.d.S.G.L.: methodology, investigation, writing-original draft. J.F.P.: writing-original draft. S.d.S.L.: validation, resources, supervision, funding acquisition. H.I.d.A.-J.: validation, resources, supervision. F.B.P.: validation, resources, supervision, funding acquisition.

Funding

This study was financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001.

References

Anderson, R.C. (2000) Nematode parasites of vertebrates: their development and transmission. CABI Publishing, New York.CrossRefGoogle Scholar
Berto, B.P., Mcintosh, D., and Lopes, C.W.G. (2014) Studies on coccidian oocysts (Apicomplexa: Eucoccidiorida). Revista Brasileira de Parasitologia Veterinária 23(1): 115. https://doi.org/10.1590/s1984-29612014001CrossRefGoogle ScholarPubMed
Callen, E.O. (1967). Analysis of Tehuacan coprolites. In: Macneish, R.S., Byers, D.S. The Prehistory of the Tehuacan Valley: Volume One Environment and Subsistence, University of Texas Press, Great Britain, pp 261289.Google Scholar
Camacho, M., Pessanha, T., Leles, D., Dutra, J.M.F., Silva, R., Souza, S.M., and Araujo, A. (2013) Lutz’s spontaneous sedimentation technique and the paleoparasitological analysis of sambaqui (shell mound) sediments. Mem Inst Oswaldo Cruz 108: 155159. https://doi.org/10.1590/0074-0276108022013005CrossRefGoogle ScholarPubMed
Carrera-Játiva, P.D., Rodríguez-Hidalgo, R., Sevilla, C., and Jiménez-Uzcátegui, G. (2014) Gastrointestinal parasites in the Galápagos Penguin Spheniscus mendiculus and the flightless cormorant Phalacrocorax Harrisi in the Galápagos Islands. Marine Ornithology 42(1): 7780.Google Scholar
Cardia, D.F.F., Bertini, R.J., Camossi, L.G., and Letizio, L.A. (2018) The first record of Ascaridoidea eggs discovered in Crocodyliformes hosts from the Upper Cretaceous of Brazil. Revista Brasileira de Paleontologia 21(3): 238244. https://doi.org/10.4072/rbp.2018.3.04CrossRefGoogle Scholar
Cardia, D.F.F., Bertini, R.J., Camossi, L.G., and Letizio, L.A. (2019) Two new species of ascaridoid nematodes in Brazilian Crocodylomorpha from the Upper Cretaceous. Parasitology International 72: 15. https://doi.org/10.1016/j.parint.2019.101947CrossRefGoogle ScholarPubMed
Carmo, G.M., Garcia, R.A., Vieira, F.M., Lima, S.S., Araújo-Júnior, H.I., and Pinheiro, R.M. (2023) Paleoparasitological study of avian trace fossils from the Tremembé Formation (Oligocene of the Taubaté Basin), São Paulo, Brazil. Journal of South American Earth Sciences 125: 18. https://doi.org/10.1016/j.jsames.2023.104319Google Scholar
Carmo, G.M., Berto, B.P., Pereira, F.B., Lima, S.S., Araújo-Júnior, H.I., and Pinheiro, R.M. (2024a) Protozoan parasites of birds from the Tremembé Formation (Oligocene of the Taubaté Basin), São Paulo, Brazil. International Journal of Paleopathology 45: 4654. https://doi.org/10.1016/j.ijpp.2024.04.003CrossRefGoogle ScholarPubMed
Carmo, G.M., Lima, S.S., Araújo-Júnior, H.I., and Pereira, F.B. (2024b) Paleoparasitological contributions to the study on ancient infections of hominids and other vertebrates in Brazil: a review. Paleontologia em Destaque - Boletim da Sociedade Brasileira de Paleontologia 38(79):4561. https://doi.org/10.4072/paleodest.2023.38.79.04CrossRefGoogle Scholar
Carmo, G.M., Lima, S.S., Araújo-Júnior, H.I., Pinheiro, R.M., Melo, D.J., and Couto-Ribeiro, G. (2024c) Paleo-faunistic checklist of the Tremembé Formation (Oligocene of the Taubaté Basin, Paraíba Valley, Brazil). Terrae Didatica 20: 111. https://doi.org/10.20396/td.v20i00.8674375CrossRefGoogle Scholar
Carvalho, E.L., Santana, R.L.S., Gonçalves, E.C., Pinheiro, R.H.S., and Giese, E.G. (2020) First report of Anisakis sp. (Nematoda: Anisakidae) parasitizing Muscovy duck in Marajó Island, state of Pará, Brazil. Braz J Vet Parasitol 29(2): 19. https://doi.org/10.1590/S1984-29612020015Google ScholarPubMed
Castro, A.C.J., Fernandes, A.C.S., and Carvalho, I.S. (1988) Coprólitos de aves da Bacia de Taubaté, SP. In: Congresso Brasileiro de Geologia, 35, 1988, Belém. Anais […] Belém: Sociedade Brasileira de Geologia. v. 6. p. 23582370. Available at: https://www.researchgate.net/publication/236345336_Coprolitos_de_aves_da_Bacia_de_Taubate_SP. Accessed 14 March 24.Google Scholar
Dentzien-Dias, P.C., Poinar, G. Jr, Figueiredo, A.E.Q., Pacheco, A.C.L., Horn, B.L.D., and Schultz, C.L. (2013) Tapeworm eggs in a 270 million-year-old shark coprolite. PLOS ONE 8(1): 14. https://doi.org/10.1371/journal.pone.0055007CrossRefGoogle Scholar
Fayer, R. (1980) Epidemiology of protozoan infections: the coccidia. Veterinary Parasitology 6(1-3): 75103. https://doi.org/10.1016/0304-4017(80)90039-4CrossRefGoogle Scholar
Ferreira, L.F., Reinhard, K.J., and Araújo, A. (2014) Foundations of Paleoparasitology. Fiocruz, Rio de Janeiro.CrossRefGoogle Scholar
Fugassa, M.H., Araújo, A., and Guichón, R.A. (2006) Quantitative paleoparasitology applied to archaeological sediments. Mem Inst Oswaldo Cruz 101(Suppl.II): 2933. https://doi.org/10.1590/s0074-02762006001000006CrossRefGoogle ScholarPubMed
Gibbons, L.M. (2010) Keys to the Nematode parasites of vertebrates: Supplementary Volume. Wallingford: CABI Publishing.Google Scholar
Gonçalves, M.L.C., Araújo, A., and Ferreira, L.F. (2003) Human intestinal parasites in the past: new findings and a review. Mem Inst Oswaldo Cruz 98: 103118. https://doi.org/10.1590/S0074-02762003000900016CrossRefGoogle ScholarPubMed
Guedes, L., Borba, V.H., Camacho, M., Neto, J., Dias, O., and Iñiguez, A.M. (2020) African helminth infection out of Africa: paleoparasitological and paleogenetic investigations in Pretos Novos cemetery, Rio de Janeiro, Brazil (1769–1830). Acta Tropica 205: 16. https://doi.org/10.1016/j.actatropica.2020.105399CrossRefGoogle Scholar
Hartwich, G. (2009) Ascaridida: Ascaridoidea. In: Anderson, R.C., Chabaud, A.G., Willmott, S. (eds). Keys to the Nematode parasites of vertebrates: Archival Volume, CABI Publishing, Wallingford, pp 309323.CrossRefGoogle Scholar
Herreras, M.V., Montero, F.E., Marcogliese, D.J., Raga, J.A., and Balbuena, J.A. (2007) Phenotypic tradeoffs between egg number and egg size in three parasitic anisakid nematodes. Oikos 116(10):17371747. https://doi.org/10.1111/j.0030-1299.2007.16016.xCrossRefGoogle Scholar
Hodda, M. (2022) Phylum Nematoda: a classification, catalogue and index of valid genera, with a census of valid species. Zootaxa 5114(1): 001289. https://doi.org/10.11646/zootaxa.5114.1.1CrossRefGoogle ScholarPubMed
Hoffman, W.A., Pons, J.A., and Janer, J.L. (1934) The sedimentation concentration method in schistosomiasis mansoni. Puet Rico J Publ Health Trop Med 9: 283289.Google Scholar
Huizinga, H.W. (1967) The Life Cycle of Contracaecum multipapillatum (von Drasche, 1882) Lucker, 1941 (Nematoda: Heterochelidae). The Journal of Parasitology 53(2):368375. https://doi.org/10.2307/3276593CrossRefGoogle ScholarPubMed
Iñiguez, A.M., Brito, L., Guedes, L., and Chaves, S.A.M. (2022) Helminth infection and human mobility in sambaquis: paleoparasitological, paleogenetic, and microremains investigations in Jabuticabeira II, Brazil (2890±55 to 1805±65 BP). The Holocene 32: 200207. https://doi.org/10.1177/09596836211060490CrossRefGoogle Scholar
Jaeger, L.H., Taglioretti, V., Dias, O., and Iñiguez, A.M. (2013a) Paleoparasitological analysis of human remains from a European cemetery of the 17th–19th century in Rio de Janeiro, Brazil. International Journal of Paleopathology 3: 214217. https://doi.org/10.1016/j.ijpp.2013.04.001CrossRefGoogle ScholarPubMed
Jaeger, L.H., Taglioretti, V., Fugassa, M.H., Dias, O., Neto, J., and Iñiguez, A.M. (2013b) Paleoparasitological results from XVIII century human remains from Rio de Janeiro, Brazil. Acta Tropica 125: 282286. https://doi.org/10.1016/j.actatropica.2012.11.007CrossRefGoogle ScholarPubMed
Koie, M., and Fagerholm, H.-P. (1995) The life cycle of Contracaecum osculatum (Rudolphi, 1802) sensu stricto (Nematoda, Ascaridoidea, Anisakidae) in view of experimental infections. Parasitol Res 81(6): 481489. https://doi.org/10.1007/bf00931790CrossRefGoogle ScholarPubMed
Leles, D., Araújo, A., Ferreira, L.F., Vicente, A.C.P., and Iñiguez, A.M. (2008) Molecular paleoparasitological diagnosis of Ascaris sp. from coprolites: new scenery of ascariasis in pre-Columbian South America times. Mem Inst Oswaldo Cruz 103: 106108. https://doi.org/10.1590/s0074-02762008005000004CrossRefGoogle ScholarPubMed
Li, L., , L., Nadler, S.A., Gibson, D.I., Zhang, L.P., Chen, H.X., Zhao, W.T., and Guo, Y.N. (2018) Molecular phylogeny and dating reveal a terrestrial origin in the early Carboniferous for Ascaridoid Nematodes. Syst Biol 67(5): 888900. https://doi.org/10.1093/sysbio/syy018CrossRefGoogle ScholarPubMed
Olson, S.L., and Alvarenga, H.M.F. (2002) A new genus of small teratorn from the Middle Tertiary of the Taubaté Basin, Brazil (Aves: Teratornithidae). Proc Biol Soc 115(4): 701705.Google Scholar
Poinar, G. Jr, and Boucot, A.J. (2006) Evidence of intestinal parasites of dinosaurs. Parasitology 133(2): 245249. https://doi.org/10.1017/S0031182006000138CrossRefGoogle ScholarPubMed
Sianto, L., Souza, M.V., Chame, M., Luz, M.F., Guidon, N., Pessis, A., and Araújo, A. (2014) Helminths in feline coprolites up to 9000 years in the Brazilian Northeast. Parasitology International 63: 851857. https://doi.org/10.1016/j.parint.2014.08.002CrossRefGoogle ScholarPubMed
Silva, P.A., Borba, V.H., Dutra, J.M.F., Leles, D., Da-Rosa, A.A.S., Ferreira, L.F., and Araujo, A. (2014) A new ascarid species in cynodont coprolite dated of 240 million years. Anais da Academia Brasileira de Ciências 86(1): 265269. https://doi.org/10.1590/0001-3765201320130036CrossRefGoogle ScholarPubMed
Souto, P.R.F. (2017) Icnologia de Paleovertebrados. Rio de Janeiro: Letra Capital.Google Scholar
Figure 0

Figure 1. Avian coprolite with fish bone fragments (A), eimeriid oocyst (B), Contracaecum egg (C), and fossilized egg of Ascaridoidea (C) from the Tremembé Formation, Taubaté Basin, State of São Paulo, Brazil.

Supplementary material: File

do Carmo et al. supplementary material

do Carmo et al. supplementary material
Download do Carmo et al. supplementary material(File)
File 2 MB