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Ferns and lycophytes in Chapada das Mesas National Park and surroundings, Maranhão State, Brazil

Samambaias e licófitas do Parque Nacional da Chapada das Mesas e arredores, Estado do Maranhão, Brasil

Abstract:

In Brazil, the number of floristic inventories involving ferns and lycophytes in the Cerrado domain is considerable. However, most of the diversity is recorded for states in the Central-West Region. In addition to the Cerrado domain, Maranhão State contains part of Amazonia and a small portion of the Caatinga. However, for this state, ferns and lycophytes are poorly sampled in floristic studies and data related to the diversity of these species are insufficient. Due to the scarcity of data about these groups, conducting floristic inventories in the state is extremely important, mainly in protected areas that contain regional vegetation near primary vegetation. Thus, the objective of the present study was to conduct a floristic inventory of the fern and lycophyte species in Chapada das Mesas National Park. We identified 86 species: 69 species of ferns, distributed in 35 genera and 17 families; and 17 species of lycophytes, distributed in five genera and three families. Among the species identified, five are new records for the Northeast Region of Brazil, twenty-one are new records for Maranhão State and eleven are new records for the Cerrado; until now, these were only recorded for Amazonia and the Atlantic Forest. The most representative families were Pteridaceae with 14 species, Selaginellaceae with 12 species, Thelypteridaceae with 11 species, and Anemiaceae, Hymenophyllaceae and Dryopteridaceae with six species each. The rupicolous life form was predominant. The new occurrence records for the Cerrado, Northeast Region and Maranhão are evidence that floristic research of ferns and lycophytes is still insufficient in these areas, and a greater sampling effort is needed to increase what is known about the diversity of these plants.

Keywords:
Cerrado; Riparian forest; Northeast; Vascular plants; Rupicolous

Resumo:

No Brasil o número de inventários florísticos envolvendo samambaias e licófitas no domínio Cerrado são consideráveis. Entretanto, a maior parte dessa diversidade é registrada para os estados da região Centro-Oeste. Além do domínio Cerrado, o território do estado do Maranhão inclui parte da Amazônia e uma pequena porção da Caatinga. No entanto, para este estado, samambaias e licófitas são pouco amostradas nos estudos florísticos e os dados relacionados à diversidade dessas espécies são insuficientes. Devido à escassez de dados sobre esses grupos, a realização de inventários florísticos no estado é de extrema importância, principalmente em unidades de conservação que contêm vegetação regional similar à vegetação primária. Assim, o objetivo do presente estudo foi realizar um inventário florístico das espécies de samambaias e licófitas no Parque Nacional da Chapada das Mesas. Nós identificamos 86 espécies: 69 espécies de samambaias, distribuídas em 35 gêneros e 17 famílias; e 17 espécies de licófitas, distribuídas em cinco gêneros e três famílias. Dentre as espécies identificadas, cinco são novos registros para a região Nordeste do Brasil, vinte e uma são novos registros para o Estado do Maranhão e onze são novos registros para o Cerrado; até agora, esses foram registrados apenas para a Amazônia e a Mata Atlântica. As famílias mais representativas foram Pteridaceae com 14 espécies, Selaginellaceae com 12 espécies, Thelypteridaceae com 11 espécies e Anemiaceae, Hymenophyllaceae e Dryopteridaceae com seis espécies cada. A forma de vida rupícola foi predominante. Os novos registros de ocorrência para o Cerrado, Nordeste e Maranhão evidenciam que a pesquisa florística de samambaias e licófitas ainda é insuficiente nessas áreas, sendo necessário um maior esforço amostral para aumentar o conhecimento em relação a diversidade dessas plantas.

Palavras-chave:
Cerrado; Mata ciliar; Nordeste; Plantas vasculares; Rupícolas

Introduction

Ferns and lycophytes are seedless vascular plants that reproduce from spores (Schuettpelz & Pryer 2008SCHUETTPELZ, E. & PRYER, K. 2008. Fern phylogeny. In: Biology and evolution of ferns and lycophytes (T.A. Ranker and C.H. Haufler, Eds). Cambridge: Cambridge University Press. p. 395-416.). They occur as various life forms, of which the most common are terrestrial, epiphytic, rupicolous and aquatic, and this has allowed them to widely colonize environments worldwide, excepts for the poles (Mehltreter 2008MEHLTRETER, K. 2008. Phenology and habitat specificity of tropical ferns. In: Biology and Evolution of Ferns and Licophytes (RANKER, T.A. & HAUFLER, C.H. (Eds.). New York: Cambridge University Press. p. 201-221., Zuquim et al. 2008ZUQUIM, G., COSTA, F.R.C., PRADO, J. & TUOMISTO, H. 2008. Guia de Samambaias e Licófitas da REBIO Uatumã. Manaus: Attema. p. 320.).

For the world, the PPG I (2016)PPG I. The Pteridophyte Phylogeny Group. 2016. A community-derived classification for extant lycophytes and ferns. J. Syst. Evol. 54 (6): 563-603. classified ferns and lycophytes into two classes, 14 orders, 51 families, 337 genera, and 11,916 species. In Brazil, it is estimated that there are 1,403 species, including 315 species in the Cerrado phytogeographic domain, which represents 22.45% of the species in Brazil (Samambaias e Licófitas in Flora do Brasil 2020SAMAMBAIAS E LICÓFITAS in Flora do Brasil 2020. Jardim Botânico do Rio de Janeiro. Available in: <http://floradobrasil.jbrj.gov.br/reflora/floradobrasil/FB128483>. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/reflora...
). Floristic inventories of these groups in the Cerrado have mostly been conducted in the Southeast and Central-West regions of Brazil (e.g., Athayde Filho & Felizardo 2010ATHAYDE FILHO, F.P. & FELIZARDO, M.P.P. 2010. Análise Florística E Ecológica Das Samambaias e Licófitas da Principal Nascente do Rio Pindaíba, Mato Grosso. Pesqui. Bot. 61: 229-244., Forsthofer & Athayde Filho 2012FORSTHOFER, M. & ATHAYDE-FILHO, F.P. 2012. Florística e aspectos ecológicos de samambaias e licófitas ao longo do córrego Cachoeirinha, Nova Xavantina-MT. Pesqui. Bot. 63: 149-164., Miguez et al. 2013MIGUEZ, F. A., KREUTZ, C. & ATHAYDE FILHO, F. P. 2013. Samambaias e licófitas em quatro matas de galeria do município de Nova Xavantina, Mato Grosso, Brasil. Pesqui. Bot. 64: 243-258.).

The Cerrado occupies 21% of Brazil and is the second largest biome in the country; only Amazonia is larger. It is a world biodiversity hotspot (Myers et al. 2000MYERS, N., MITTERMEIER, R.A., MITTERMEIER, C.G. FONSECA, G.A.B. & KENT, J. 2000. Biodiversity hotspots for conservation priorities. Nature 403: 853-858., Silva & Bates 2002SILVA, J.M.C. & BATES, J.M. 2002. Biogeographic patterns and conservation in the South American Cerrado: a tropical savanna hotspot. BioScience 52: 225-233.) and widely used for agricultural activities (Borlaug 2002BORLAUG, N.E. 2002. Feeding a world of 10 billion people: the miracle ahead. In: R. Bailey (ed.). Global warming and other eco-myths. p. 29-60. Competitive Enterprise Institute, Roseville, EUA.). Although a large part of the Cerrado is extremely important to the conservation of biodiversity, only 5.5% of its original area consists of protected areas (PAs). Further, it is the world hotspot with the lowest percentage of areas that are completely protected (Brasil, Mittermeier et al. 2021MITTERMEIER, R.A., GIL, P.R., HOFFMANN, M., PILGRIM, J., BROOKS, T., MITTERMEIER, C.G., LAMOUREX, J. & FONSECA, G.A.B. 2021. Hotspots Revisitados. Publicação produzida pela Conservação Internacional Brasil com base no livro Hotspots Revisited. Earth’s Biologically Richest and Most Endangered Terrestrial Ecorregions. Available in: https://www.conservation.org/docs/default-source/brasil/HotspotsRevisitados.pdf (last access 06/05/2021).
https://www.conservation.org/docs/defaul...
).

In addition to the Cerrado domain, Maranhão contains other phytogeographic domains (i.e., a portion of Amazonia and a small part of the Caatinga) and extensive transition areas between them, resulting in high biodiversity in the state. However, the biodiversity in Maranhão, especially lycophytes and ferns, could be underestimated because not many areas have been sampled and studied (Table 1) (e.g., Bastos & Cutrim 1999BASTOS, C.C.C. & CUTRIM, M.V.J. 1999. Pteridoflora da Reserva florestal do Sacavém, São Luis - Maranhão. Bol. Mus. Para. Emílio Goeldi, sér. Bot. 15(1): 3-37., Azevedo & Silva 2001AZEVEDO, A.C.G. & SILVA, W.M. 2001. Ocorrência de Lycopodiella cernua (L.) Pic. Serm. (Pteridophyta: Lycopodiopsida: Lycopodiaceae) nas bordas de manguezal, São Luís - Maranhão - Brasil. Bol. Lab. Hidrobiol. 14(1): 111-114., Fernandes et al. 2007FERNANDES, R.S., CONCEIÇÃO, G.M., BRITO E.S. & PAULA-ZÁRATE, E.L. 2007. Diversidade Florística de Pteridófitas da Área de Preservação Ambiental do Inhamum, Caxias, Maranhão, Brasil. Rev. bras. Bioci. 5(2): 411-413., 2010FERNANDES, R.S., CONCEICÃO, G.M., COSTA J.M. & PAULA-ZÁRATE, E.L. 2010. Samambaias e licófitas do município de Caxias, Maranhão, Brasil. Bol. Mus. Emílio Goeldi. Ciênc. Nat. (3): 345-356., Conceição & Ruggieri 2010CONCEIÇÃO, G.M. & RUGGIERI, A.C. 2010. Pteridófitas do município de Tufilândia, Estado do Maranhão, Brasil. Pesquisa em Foco. 18(1): 59-68., Conceição & Rodrigues 2010CONCEIÇÃO, G.M. & RODRIGUES, M.S. 2010. Pteridófitas do Parque Estadual do Mirador, Maranhão, Brasil. Cad. Geociênc. (7): 47-53., Conceição et al. 2015CONCEIÇÃO, G.M., PAULA-ZARATE, E.L., RUGGIERI, A.C., SILVA, E.O. & SILVA, M.F. 2015. Pteridoflora e seus aspectos ecológicos no município de Timon, Maranhão, Brasil. Braz. Geogr. J. 6(1): 74-81., Santos-Silva 2016SANTOS-SILVA, D.L. 2016. Cyathea delgadii Sternb. (Cyatheaceae, Samambaia): Caracterização e Ecologia Populacional no Domínio Fitogeográfico do Cerrado/ Dissertação (Mestrado) - Centro de Estudos Superiores de Caxias, Curso de Pós-graduação em Biodiversidade, Ambiente e Saúde., Silva et al. 2017SILVA, G.S., SILVA, D.L.S., OLIVEIRA, R.R., SILVA, M.L.A. & CONCEIÇÃO, G.M. 2017. Licófitas e samambaias no cerrado do leste do Maranhão, Brasil. Acta Bra. 1(2): 13-16., Santos-Silva et al. 2018SANTOS-SILVA, D.L., SILVA, G.S., OLIVEIRA, R.R. & CONCEIÇÃO, G.M. 2018. Nova ocorrência de Lycopodiaceae (Lycophyta) para o Estado do Maranhão: Pseudolycopodiella carnosa (Silveira) Holub. Biota Amazônia 8(2): 58-59., Silva-Júnior et al. 2018, Santos-Silva et al. 2019aSANTOS-SILVA, D.L., OLIVEIRA, R.F., CONCEIÇÃO, G.M. 2019a. Formigas associadas à Cyathea delgadii Sternb. (Cyatheaceae) em um fragmento de Cerrado maranhense, Nordeste, Brasil. Biota Amazônia 9(1): 34-36., b, c, Barbieri et al. 2020BARBIERI, R., LIMA, L.B.C. & CORREIA, M.M.F. 2020. Distribuição, morfologia e anatomia de monilófitas (samambaias) aquáticas de pequenas lagoas na área Itaqui-Bacanga, Ilha de São Luís - MA. Bol. Lab. Hidrobiol. 30 (2): 1-12., Almeida et al. 2020ALMEIDA, F.C., PIETROBOM, M, R. & FERNANDES, R.S. 2020. Lycophytes of the Chapada das Mesas National Park, Cerrado, Maranhão, Brazil. Biota Neotropica 20(3): 1-11., Silva-Junior et al. 2020SILVA-JUNIOR, W.R., FERREIRA, A.W.C., ILKIU-BORGES, A.L. & FERNANDES, R.S. 2020. Ferns and lycophytes of remnants in Amazônia Maranhense, Brazil. Biota Neotropica 20(3): 1-14.). According to Samambaias e Licófitas in Flora do Brasil (2020)SAMAMBAIAS E LICÓFITAS in Flora do Brasil 2020. Jardim Botânico do Rio de Janeiro. Available in: <http://floradobrasil.jbrj.gov.br/reflora/floradobrasil/FB128483>. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/reflora...
, only 97 species of ferns and lycophytes have been recorded in Maranhão. However, based on a compilation of data published in floristic inventories about the state (mentioned above), there are 24 families and 130 species (Supplementary file 1). Among the studies cited above, most sampling was conducted in the Amazon domain (64 species) (e.g., Silva Junior et al. 2020), which includes an important federal protected area called the Gurupi Biological Reserve (Reserva Biológica do Gurupi) (Table 1).

Table 1
Scientific studies of ferns and lycophytes conducted Maranhão State. Author(s), article title, species, genus and family numbers (Quant. spp./gen./fam.), new records, size of area and phytogeographic domain.

In Maranhão State, 12.5% of the Cerrado is within PAs, of which 5.7% is completely protected under the category National Park (Parque Nacional) and 6.8% is sustainably used and mainly environmental protection areas (Áreas de Proteção Ambiental) (Spinelli-Araújo et al. 2016SPINELLI-ARAÚJO, L., BAYMA-SILVA, G., TORRESAN, F.E., VICTORIA, D., VICENTE, L.E., BOLFE, E.L. & MANZATTO, C. 2016. Conservação da Biodiversidade do Estado do Maranhão: Cenário Atual em Dados Geoespaciais. Jaguariúna, Embrapa Meio Ambiente.). In the Cerrado in the state, 74 species of ferns and lycophytes have been recorded (Fernandes et al. 2007FERNANDES, R.S., CONCEIÇÃO, G.M., BRITO E.S. & PAULA-ZÁRATE, E.L. 2007. Diversidade Florística de Pteridófitas da Área de Preservação Ambiental do Inhamum, Caxias, Maranhão, Brasil. Rev. bras. Bioci. 5(2): 411-413., 2010FERNANDES, R.S., CONCEICÃO, G.M., COSTA J.M. & PAULA-ZÁRATE, E.L. 2010. Samambaias e licófitas do município de Caxias, Maranhão, Brasil. Bol. Mus. Emílio Goeldi. Ciênc. Nat. (3): 345-356., Conceição & Ruggieri 2010CONCEIÇÃO, G.M. & RUGGIERI, A.C. 2010. Pteridófitas do município de Tufilândia, Estado do Maranhão, Brasil. Pesquisa em Foco. 18(1): 59-68., Conceição & Rodrigues 2010CONCEIÇÃO, G.M. & RODRIGUES, M.S. 2010. Pteridófitas do Parque Estadual do Mirador, Maranhão, Brasil. Cad. Geociênc. (7): 47-53., Conceição et al. 2015CONCEIÇÃO, G.M., PAULA-ZARATE, E.L., RUGGIERI, A.C., SILVA, E.O. & SILVA, M.F. 2015. Pteridoflora e seus aspectos ecológicos no município de Timon, Maranhão, Brasil. Braz. Geogr. J. 6(1): 74-81., Silva et al. 2017SILVA, G.S., SILVA, D.L.S., OLIVEIRA, R.R., SILVA, M.L.A. & CONCEIÇÃO, G.M. 2017. Licófitas e samambaias no cerrado do leste do Maranhão, Brasil. Acta Bra. 1(2): 13-16., Santos-Silva et al. 2019bSANTOS-SILVA, D.L., GOMES, G.S., SILVA, G.S., OLIVEIRA, R.F., MARTINS, P.R.P., SOUSA, D.H.S., ARAÚJO, M.F.V. & CONCEIÇÃO, G.M. 2019b. New occurrences of Schizaeaceae for the Maranhão and Brazilian Cerrado. International Journal of Development Research 9(4): 26857-26862., c, Almeida et al. 2020ALMEIDA, F.C., PIETROBOM, M, R. & FERNANDES, R.S. 2020. Lycophytes of the Chapada das Mesas National Park, Cerrado, Maranhão, Brazil. Biota Neotropica 20(3): 1-11., Samambaias e Licófitas in Flora do Brasil 2020SAMAMBAIAS E LICÓFITAS in Flora do Brasil 2020. Jardim Botânico do Rio de Janeiro. Available in: <http://floradobrasil.jbrj.gov.br/reflora/floradobrasil/FB128483>. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/reflora...
) (Supplementary file 1). Despite the considerable number of studies conducted, the greatest diversity recorded was 21 species for the municipality of Caxias, which includes the Inhamum Environmental Protection Area (Área de Proteção Ambiental do Inhamum) (Fernandes et al. 2007FERNANDES, R.S., CONCEIÇÃO, G.M., BRITO E.S. & PAULA-ZÁRATE, E.L. 2007. Diversidade Florística de Pteridófitas da Área de Preservação Ambiental do Inhamum, Caxias, Maranhão, Brasil. Rev. bras. Bioci. 5(2): 411-413., 2010FERNANDES, R.S., CONCEICÃO, G.M., COSTA J.M. & PAULA-ZÁRATE, E.L. 2010. Samambaias e licófitas do município de Caxias, Maranhão, Brasil. Bol. Mus. Emílio Goeldi. Ciênc. Nat. (3): 345-356.). Among the studies published, only two were conducted in completely protected PAs: an inventory of ferns and lycophytes in Mirador State Park (Parque Estadual do Mirador) (e.g., Conceição & Rodrigues 2010CONCEIÇÃO, G.M. & RODRIGUES, M.S. 2010. Pteridófitas do Parque Estadual do Mirador, Maranhão, Brasil. Cad. Geociênc. (7): 47-53.), which is the largest protected area in Maranhão State (437,000 ha); and an inventory of lycophytes conducted in Chapada das Mesas National Park (Parque Nacional da Chapada das Mesas) (e.g., Almeida et al. 2020ALMEIDA, F.C., PIETROBOM, M, R. & FERNANDES, R.S. 2020. Lycophytes of the Chapada das Mesas National Park, Cerrado, Maranhão, Brazil. Biota Neotropica 20(3): 1-11.).

Chapada das Mesas National Park (PNCM) is a protect area in Maranhão that is predominantly Cerrado, in an environment that transitions with the Caatinga and Amazon biomes (ICMBio 2021ICMBio. Plano de manejo do Parque Nacional da Chapada das Mesas. Available in: https://www.icmbio.gov.br (last access 28/06/2021).
https://www.icmbio.gov.br...
). All stratifications associated with the Cerrado biome occur in this area, including humid and dry forests, cerradão, cerrado ralo, marshes and veredas. This PA is part of the Araguaia Bananal ecological corridor, which is an important ecotone between the Cerrado and Amazon biomes (MMA 2007MMA. 2007. Ministério do Meio Ambiente. Centro Nacional de Prevenção e Combate aos Incêndios Florestais - PREVFOGO. Parque Nacional da Chapada das Mesas. Plano operativo de prevenção e combate aos incêndios florestais do Parque Nacional da Chapada das Mesas. Brasília: MMA. Available in: https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&ved=2ahUKEwinx8btjKnyAhVTqpUCHSXMB3sQFnoECAIQAQ&url=http%3A%2F%2Fibama.gov.br%2Fphocadownload%2Fprevfogo%2Fplanos_operativos%2Fplano_operativo_parna_da_chapada_das_mesas.pdf&usg=AOvVaw1dXtGszGTvpSvsduxqgzTa (last access 10/08/2021).
https://www.google.com/url?sa=t&rct=j&q=...
).

Despite being created over 15 years ago and possessing diverse phytophysiognomies of the Cerrado domain, including large areas of field and savanna formations, the management plan of the park lacks data about the floristic diversity ( MMA 2012MINISTÉRIO DO MEIO AMBIENTE - MMA. 2012. Plano de proteção anual do Parque Nacional da Chapada das Mesas. ICMbio., ICMBio 2021ICMBio. Plano de manejo do Parque Nacional da Chapada das Mesas. Available in: https://www.icmbio.gov.br (last access 28/06/2021).
https://www.icmbio.gov.br...
). Further, studies about the plant diversity of the area are recent (e.g., Silva et al. 2018SILVA, J.A.S., FERNANDES, R.S. & COSTA, D.P. 2018. Species diversity of the genus Riccia L. (Marchantiales, Ricciaceae) in Maranhão state, Brazil. Check List 14 (5): 763-769., Oliveira et al. 2018OLIVEIRA, R.R., OLIVEIRA, R.F., OLIVEIRA, H.C., PERALTA, D.F. & CONCEIÇÃO, G.M., 2018. Pleurocarpous and cladocarpous mosses (Bryophyta) of Parque Nacional da Chapada das Mesas, with newly recorded species from Maranhão and the northeast region of Brazil. Check List 16 (6): 1733-1745., Fernandes et al. 2021FERNANDES, R.S., SILVA, J.A.S., OTTONI, F.P. & COSTA, D.P. 2021. Diversity of thalloid liverworts in Brazilian Savanna of Parque Nacional da Chapada das Mesas, Maranhão, Brazil. Check List 17(1): 45-58., Silva et al. 2021SILVA, J.P, OLIVEIRA-DA-SILVA, F.R, ILKIU-BORGESAL & FERNANDES, R.S. 2021. Leafy liverworts of Chapada das Mesas National Park: a floristic survey and checklist of the leafy liverworts of Maranhão state, Brazil. Check List 17 (2): 479-495.) and only one is about vascular plants (e.g., Almeida et al. 2020ALMEIDA, F.C., PIETROBOM, M, R. & FERNANDES, R.S. 2020. Lycophytes of the Chapada das Mesas National Park, Cerrado, Maranhão, Brazil. Biota Neotropica 20(3): 1-11.).

Thus, the objective of this work was to conduct a floristic survey in PNCM, an extremely important region for the conservation of biodiversity in the Cerrado that is in a transition area, with the goal of providing new information about the ferns and lycophytes of the Cerrado domain and Brazil. This data will contribute to future works about ecology, conservation and environmental education in the area, as well as the management plan for the park.

Material and Methods

1. Study area

The Chapada das Mesas National Park, comprises approximately 160,000 ha of Cerrado divided into two polygons, one with around 120,000 ha and another with about 40,000 ha, which are distributed in the municipalities of Carolina, Riachão and Estreito in southeastern Maranhão State (Brasil 2006BRASIL, 2006. Decreto s/n, de 12 de dezembro de 2005. https://www.ibama.gov.br/component/legislacao/?view=legislacao&force=1&legislacao=112238 (last access 12/03/2021).
https://www.ibama.gov.br/component/legis...
, ICMbio 2021ICMBio. Plano de manejo do Parque Nacional da Chapada das Mesas. Available in: https://www.icmbio.gov.br (last access 28/06/2021).
https://www.icmbio.gov.br...
).

The climate is predominantly seasonal tropical, type Aw (Köppen 1948KÖPPEN, W. 1948. Climatologia: con un estudio de los climas de la tierra. Fundo de Cultura Economica, México, p.478.), with a dry season for 3 to 5 months and a rainy season with average rainfall ranging from 1,250 to 1,500 mm, an average annual temperature between 20ºC and 27ºC and average relative air humidity of approximately 60% (Pereira et al. 2011PEREIRA, B.A.S., VENTUROLI, F. & CARVALHO, F.A. 2011. Florestas Estacionais no Cerrado: Uma Visão Geral. Pesq. Agropec. Trop. 41(3): 446-455.).

Hydrologically, the area is very rich. The main watercourses are the Farinha River (norther portion) and Itapecuru River (southern portion), there are over 400 springs in the interior, and along the watercourses there are well-conserved riparian forests (ICMBio 2021ICMBio. Plano de manejo do Parque Nacional da Chapada das Mesas. Available in: https://www.icmbio.gov.br (last access 28/06/2021).
https://www.icmbio.gov.br...
).

The relief is characterized by the presence of sandstone and typical forms of paleokarst in sandstone (e.g., hilltop arches, small cavities, canyons, paleosinkholes, sinkholes and river resurgences), which is closely related to the evolution of the subterranean drainage and river incision (Martins et al. 2017MARTINS, F.P., SALGADO, A.A.R. & BARRETO, H.N. 2017. Morfogênese da Chapada das Mesas (Maranhão Tocantins): paisagem cárstica e poligenética. Rev. Bras. Geomorfol. 18(3): 623-635.). The soil is predominantly sandy where there are Cerrado sensu stricto and campo sujo physiognomies. However, there are also places with richer soils, mainly on the tops of mountains that have patches of semideciduous forest (ICMBio 2021ICMBio. Plano de manejo do Parque Nacional da Chapada das Mesas. Available in: https://www.icmbio.gov.br (last access 28/06/2021).
https://www.icmbio.gov.br...
).

In addition to the natural vegetation cover typical of the Cerrado biome that contains many phytophysiognomies, among which savanna and forest aspects are notable, there are also Caatinga and Amazonian species, which help characterize the high diversity of the area (ICMBio 2021ICMBio. Plano de manejo do Parque Nacional da Chapada das Mesas. Available in: https://www.icmbio.gov.br (last access 28/06/2021).
https://www.icmbio.gov.br...
). These vegetation characteristics, including the presence of well-conserved riparian forests along watercourses, large patches of cerradão and other types of phytophysiognomies, are essential for maintaining the biodiversity in the region (Marques 2012MARQUES, A.R. 2012. Saberes geográficos integrados aos estudos territoriais sob a ótica da implantação do Parque Nacional da Chapada das Mesas, sertão de Carolina - MA. Tese de doutorado. Universidade Estadual Paulista, Presidente Prudente.).

2. Data collection

The species were collected during four expeditions, in March and October 2017, June 2018 and February 2020, which were three days each and included the dry and rainy seasons. Collecting was based on the methods proposed by Filgueiras et al. (1994)FILGUEIRAS, T.S., NOGUEIRA, P.E., BROCHADO, A.L., & GUALA, G.F., 1994. Caminhamento: um método expedito para levantamentos florísticos qualitativos. Cad. Geociênc. 12(1): 39-43.. Microenvironments in the study area were selected and explored randomly, with the goal of visiting the greatest number of places where taxa might occur. The sampling points were mapped (Figure 1).

Figure 1
Localization map of the study area, showing samples sites inside and outside the Chapada das Mesas National Park (Modified from: Silva et al. 2021SILVA, J.P, OLIVEIRA-DA-SILVA, F.R, ILKIU-BORGESAL & FERNANDES, R.S. 2021. Leafy liverworts of Chapada das Mesas National Park: a floristic survey and checklist of the leafy liverworts of Maranhão state, Brazil. Check List 17 (2): 479-495.).

Herbarium specimens were made based on standard techniques used for seedless vascular plants (Silva 1989SILVA, A.T. 1989. Pteridófitas. In Técnicas de coleta, preservação e herborização de material botânico (O. Fidalgo & V.L.R. Bononi, Eds). Instituto de Botânica, São Paulo p. 32-34.). All the material was deposited in the CCAA herbarium (RBH 2019RBH. Available in: https://www.botanica.org.br/catalogo-da-rede-brasileira-de-herbarios/ (last access 27/03/2021).
https://www.botanica.org.br/catalogo-da-...
), at the Federal University of Maranhão, Campus Chapadinha. When available, duplicates were sent to the following institutions: MG, HBRA and BHCB (Thiers 2019THIERS, B. 2019. [continuously updated]. Index Herbariorum: A global directory of public herbaria and associated staff. New York Botanical Garden’s Virtual Herbarium. Available in: http://sweetgum.nybg.org/science/ih/ (last access 08/07/2021).
http://sweetgum.nybg.org/science/ih/...
).

The identification and distribution of the species and genera were based on specialized literature, such as PPG I (2016)PPG I. The Pteridophyte Phylogeny Group. 2016. A community-derived classification for extant lycophytes and ferns. J. Syst. Evol. 54 (6): 563-603., IPNI (2019)IPNI. Available in: https://www.ipni.org/ (last access 28/06/2021).
https://www.ipni.org/...
the Flora do Brasil 2020FLORA DO BRASIL 2020. Jardim Botânico do Rio de Janeiro. Available in: < http://floradobrasil.jbrj.gov.br/ >. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/...
monographs, as well as revisions and regional floras (e.g., Tryon & Stolze 1994TRYON, R.M. & STOLZE, R.G. 1994. 22. Marsileaceae - 28. Isoëtaceae. In Pteridophyta of Peru. Fieldiana Bot. 32(Part 6): 1-190., Moran & Riba 1995MORAN, R.C & RIBA, R. 1995. Flora Mesoamericana. Psilotaceae a Salviniaceae. Universidade Nacional Autônoma do México, México, v.1, p.470., Mickel & Smith 2004MICKEL, J.T. & SMITH, A.R. 2004. The Pteridophytes of Mexico. Memoirs of the New York Botanical Garden 88: 1-1054.). When needed, some species were sent to specialists to confirm the identification.

The terminology follows Lellinger (2002)LELLINGER, D.B. 2002. A modern multilingual glossary for taxonomic pteridology. American Fern Society, Washington, p.263.. Family and genus delimitations are based on PPG I (2016)PPG I. The Pteridophyte Phylogeny Group. 2016. A community-derived classification for extant lycophytes and ferns. J. Syst. Evol. 54 (6): 563-603.. Nomenclature and authors of the species follow the International Plant Names Index (IPNI 2019IPNI. Available in: https://www.ipni.org/ (last access 28/06/2021).
https://www.ipni.org/...
) and Tropicos (2019)TROPICOS. Available in: http://www.tropicos.org/Name/26616606 (last access 21/03/2021).
http://www.tropicos.org/Name/26616606...
. The images of species were taken with a digital camera in the field or from herbarium specimens (fertile parts). The photographic plates, preferentially of new records for Maranhão State, were made with Photoshop® CS6 v.13.0 (Adobe Systems 2012ADOBE SYSTEMS. 2012. Photoshop CS6. Available in: https://www.adobe.com/ (last access 16/11/2019).
https://www.adobe.com/...
). Comments about the environment of occurrence are based on the area where the material was collected. Life forms were determined based on Lellinger (2002)LELLINGER, D.B. 2002. A modern multilingual glossary for taxonomic pteridology. American Fern Society, Washington, p.263., Zuquim et al. (2008)ZUQUIM, G., COSTA, F.R.C., PRADO, J. & TUOMISTO, H. 2008. Guia de Samambaias e Licófitas da REBIO Uatumã. Manaus: Attema. p. 320. and Irgang et al. (1984)IRGANG, B.E., PEDRALLI, G. & WAECHTER, J.L. 1984. Macrófitas aquáticas da Estação Ecológica do Taim, Rio Grande do Sul, Brasil. Rossléria 6: 395-404.. For floating aquatic plants that grow exclusively in aquatic environments (e.g., lakes, ponds), without connection to the soil, we follow Pedralli et al. (1985) apud Pott et al. (1989)POTT, V.J., BUENO, N.C., PEREIRA, R.A.C. SALIS, S.M. & VIEIRA, N.L. 1989. Distribuição de macrófitas aquáticas numa lagoa na Fazenda Nhumirim, Nhecolândia, Pantanal, MS. Acta Botanica Brasilica 3(2): 153-168..

The types of phytophysiognomies (or habitat of occurrence) of the species were based on field observations and follow the classification of Flora do Brasil (2020)FLORA DO BRASIL 2020. Jardim Botânico do Rio de Janeiro. Available in: < http://floradobrasil.jbrj.gov.br/ >. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/...
. The following categories were considered:

- Open riparian forest: forest vegetation associated with watercourses that is wide with trees spaced apart; - Closed riparian forest: forest vegetation associated with watercourses that is narrower with trees closer together and a canopy; - Cerrado sensu stricto: presence of short, inclined, tortuous trees with thin trunks and irregular, twisted branches, generally with signs of past fires, and the presence of a lot of grass in the understory; - Anthropogenic area (pasture): environment where the original vegetation was destroyed in relation to the primary phytophysiognomy and transformed into pasture with babaçu palms; - Vereda: area of open marsh with grasses, buriti palms and a few shrubs, which is associated with nearby forest with watercourses.

The microenvironments preferred by the species were defined based on field observations, such as the following:

Rocky banks: located along the margins of watercourses inside forests, formed by rocks that are bare or only have a thin layer of humus, with a slight to vertical (90°) incline; - Non-rocky banks: located along the margins of watercourses inside forests, formed by various soil types (non-rocky), with a slight to vertical incline (90°); - Waterfall areas: locations near a waterfall and formed by vertical (90°) rock faces with constant water vapor; - Rock walls: blocks of continuous rock forming vertical (90°) rock extensions (taller than the banks), with bare rock or only a thin layer of humus, located along the margins of watercourses inside riparian forest or between Cerrado sensu stricto vegetation; - Marshy areas with buriti palms: locations with wet soil that are associated with watercourses inside forest where buriti palms predominate; -Marshy areas with grasses: locations with wet soil that are associated with watercourses in open areas where there are a few shrubs and grasses predominate; - Pasture with babaçu palms; - Forest interior in flat area; - Open flooded area.

Results

1. Ferns and lycophytes diversity

We identified 86 species of ferns and lycophytes: 69 species of ferns, distributed in 35 genera and 17 families; and 17 species of lycophytes, distributed in five genera and three families (Table 2 and Supplementary file 2).

Table 2
List of fern and lycophyte species in Chapada das Mesas National Park, Maranhão State, Brazil. New records for Maranhão, the Northeast Region and the Cerrado are in bold. Life form/growth, Habitat, Microenvironments.

Among the species identified, five are new records for the Northeast Region of Brazil, twenty-one are new records for Maranhão State and eleven are new records for the Cerrado of Brazil that, until now, were only recorded for Amazonia and the Atlantic Forest (Table 2 and Supplementary file 2).

The most representative families were Pteridaceae with 14 species, Selaginellaceae with 12 species, Thelypteridaceae with 11 species, and Anemiaceae, Hymenophyllaceae and Dryopteridaceae with six species each (Table 2).

Seven species were identified to the genus level, and all other species were identified to the species level. Elaphoglossum sp. was identified to the genus level since only sterile material was collected. The other six species (Selaginella sp.1, Selaginella sp.2, Selaginella sp.3, Blechnum cf. occidentale, Blechnum sp., and Adiantum sp.) were identified to the genus level due to the confusing taxonomy or probably hybrid (pers. com., Vinicius Dittrich, Luis Armando Góes Neto and Jefferson Prado).

The rupicolous life form had the highest number of species, with 22 species (58% of the total number of species), followed by terrestrial with 15 species (22% of the total), epiphytic with three species, terrestrial climber with three species, fixed aquatic with two species, and floating aquatic with one species. Forty species had more than one life form: 32 terrestrial and rupicolous; seven epiphytic and rupicolous; and one terrestrial, epiphytic and rupicolous (Table 2).

2. New records: Northeast Region, Maranhão and the Cerrado domain

Selaginella convoluta (Arn.) Spring.

(Figure 2A)

Figure 2
Habit. A. Selaginella convoluta (Arn.) Spring. B. Selaginella marginata (Humb. & Bonpl. ex Willd.) Spring. C. Selaginella minima Spring. D. Selaginella simplex Baker. Habit. E. Seleginella erythropus (Mart.) Spring. F. Selaginella sulcata (Desv. ex Poir.) Spring ex Mart. Scale bar: B; F = 2cm; C=1cm.

Rupicolous on a rocky bank in a waterfall area. Habitat: open riparian forest.

Geographic distribution: AL, BA, CE, MA, PB, PE, PI, RN, SE, GO, MS, MT, ES, MG, RJ, SP, PR (Caatinga, Cerrado and Atlantic Forest). New record: Maranhão.

Selaginella minima Spring.

(Figure 2C)

Terrestrial on a non-rocky bank and rupicolous plant collected on a rocky bank in a waterfall area, near the margin of a trail. Habitat: closed riparian forest. Geographic distribution: AM, AP, PA, RO, MA, PI, GO, MT (Amazonia and Cerrado). New record: Maranhão.

Selaginella sulcata (Desv. ex Poir.) Spring ex Mart.

(Figure 2F)

Rupicolous on a rocky bank on the top of a hill, near a watercourse. Habitat: open riparian forest, closed riparian forest. Geographic distribution: AC, AM, PA, BA, CE, MA, PB, PE, MS, MT, ES, MG, RJ, SP, PR, RS, SC (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão and Cerrado.

Lycopodiella longipes (Grev. & Hook.) Holub.

(Figure 3A)

Figure 3
Habit. A. Lycopodiella longipes (Grev. & Hook.) Holub. B. Palhinhaea camporum (B. Øllg. & Windisch) Holub. C. Pseudolycopodiella meridionalis (Underw. & Loyd) Holub.

Terrestrial in an open marshy area with grasses. Habitat: vereda. Geographic distribution: AC, AM, RR, BA, MA, DF, GO, MG, RJ, SP, PR, RS, SC (Amazonia, Cerrado, Atlantic Forest and Pampa). New record: Maranhão and Cerrado.

Palhinhaea camporum (B. Øllg. & Windisch) Holub.

(Figure 3B)

Terrestrial in an open marshy area with grasses. Habitat: vereda. Geographic distribution: AC, AM, AP, PA, RO, RR, TO, BA, MA, PE, PI, DF, GO, MS, MT, MG, SP, PR, SC (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Anemia buniifolia (Gardner) T.Moore.

(Figure 4A)

Figure 4
A. Anemia buniifolia (Gardner) T.Moore. Habit. B. Anemia elegans (Gardner) C.Presl. Habit. C. Anemia hirsuta (L.) Sw. Habit. D. Anemia oblongifolia (Cav.) Sw. Habit. E. Blechnum cf. occidentale. Habit. F. Blechnum sp. Habit. G. Salpichlaena hookeriana (Kuntze) Alston. Habit. H. Pteridium esculentum (G.Forst.) Cockayne subsp. gryphus Schwartsb. var. harpianum Schwartsb. & A.Yanez. Sterile Pinnae. Scale bar: A; H = 2cm.

Rupicolous near the margin of a trail on a rocky bank in a waterfall area. Habitat: open riparian forest. Geographic distribution: AM, PA, TO, BA, MA, DF, GO, MT, MG (Amazonia and Cerrado). New record: Maranhão.

Anemia elegans (Gardner) C.Presl.

(Figure 4B)

Rupicolous on a rock wall and in rock cracks on the margin of a trail. Habitat: Cerrado sensu stricto. Geographic distribution: TO, BA, MA, DF, GO, MT, MG (Cerrado). New record: Maranhão.

Anemia trichorhiza Gardner.

Illustration.Mickel (2016MICKEL, J.T. 2016. Anemia (Anemiaceae). The New York Botanical Garden. Flora Neotropica Monograph 118: 1-192.: 126, fig. 13A-C).

Rupicolous on a rock wall on the margin of a trail. Habitat: Cerrado sensu stricto. Geographic distribution: MA, DF, GO, MS, MT, MG, SP, PR (Cerrado and Pantanal). New record: Northeast Region.

Salpichlaena hookeriana (Kuntze) Alston

(Figure 4G)

Terrestrial climber growing on a rocky bank near a waterfall area. Habitat: closed riparian forest. Geographic distribution: AC, AM, PA, MA, RO, MS, MT (Amazonia and Cerrado). New record: Northeast Region and Cerrado.

Bolbitis serratifolia Schott.

(Figure 5A)

Figure 5
A. Bolbitis serratifolia Schott. Habit. B. Cyclodium meniscioides (Willd.) C. Presl. Habit. C. Dryopteris patula (Sw.) Underw. Habit. D. Elaphoglossum scalpellum (Mart.) T. Moore. Sterile fronds. E. Polybotrya sorbifolia Mett. ex Kuhn. F-G. Didymoglossum angustifrons Fée. F. Habit. G. Fertile frond. H. Didymoglossum pinnatinervium (Jenman) Pic.Serm. Fertile frond I. Trichomanes arbuscula Desv. Habit. Scale bar: D = 2cm.

Rupicolous on a rock wall near a waterfall area. Habitat: closed riparian forest. Geographic distribution: AC, AM, PA, RO, CE, MA, GO, MS, MT, ES, MG, RJ, SP, PR, RS, SC (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão and Cerrado.

Cyclodium meniscioides (Willd.) C. Presl

(Figure 5B)

Terrestrial in a marshy area with buriti palms and rupicolous plant in a waterfall area. Habitat: closed riparian forest. Geographic distribution: AC, AM, AP, PA, RO, TO, BA, CE, MA, PB, PE, PI, RN, DF, GO, MS, MT, ES, MG, SP (Cerrado and Atlantic Forest). New record: Maranhão.

Dryopteris patula (Sw.) Underw.

(Figure 5C)

Rupicolous on a rock wall on the margin of a watercourse. Habitat: closed riparian forest. Geographic distribution: AC, AM, AP, PA, RO, BA, MA, PI, GO, MT, ES, MG, RJ, SP, PR, RS, SC (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Elaphoglossum scalpellum (Mart.) T. Moore.

(Figure 5D)

Rupicolous on a rock wall and near a waterfall area. Habitat: closed riparian forest. Geographic distribution: AM, RO, TO, BA, MA, PI, DF, GO, MT, MG, SP (Cerrado). New record: Maranhão.

Polybotrya sorbifolia Mett. ex Kuhn.

(Figure 5E)

Rupicolous on a rock wall. Habitat: closed riparian forest. Geographic distribution: PA, RO, AL, MA, PE, GO, MT, MG, SP (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Didymoglossum angustifrons Fée

(Figure 5F-G)

Epiphytic from the base of a trunk of a live tree and rupicolous plant on a rocky bank in a waterfall area. Habitat: closed riparian forest. Geographic distribution: AM, AP, PA, RO, BA, MA, CE, MT, MG, RJ, SP, PR (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Didymoglossum pinnatinervium (Jenman) Pic.Serm.

(Figure 5H)

Rupicolous on a rocky bank in a waterfall area. Habitat: closed riparian forest. Geographic distribution: MA (Cerrado). New record: Northeast Region and Cerrado.

Trichomanes arbuscula Desv.

(Figure 5I)

Rupicolous on a rocky bank. Habitat: closed riparian forest. Geographic distribution: AC, AM, AP, PA, BA, MA, PE, MT, ES (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão and Cerrado.

Lindsaea pallida Klotzsch

(Figure 6B)

Figure 6
A. Lindsaea guianensis subsp. lanceastrum K.U.Kramer. Habit. B. Lindsaea pallida Klotzsch. Fertile frond. C. Serpocaulon triseriale (Sw.) A.R.Sm. Habit. D. Metaxya parkeri (Hook. & Grev.) J. Sm.. Habit. E. Microgramma persicariifolia (Schrad.) C.Presl. Habit. Scale bar: B = 2cm.

Terrestrial on a sandy bank near the margin of a river. Habitat: closed riparian forest. Geographic distribution: AC, AM, AP, PA, BA, MA, PE, MT (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Metaxya parkeri (Hook. & Grev.) J. Sm.

(Figure 6D)

Terrestrial on a sandy bank with litter and rupicolous plant on rock walls near watercourses, such as creek banks and waterfalls. Habitat: closed riparian forest. Geographic distribution: AC, AM, AP, PA, BA, MA, PE, MT (Amazonia, Cerrado and Atlantic Forest). New record: Cerrado.

Nephrolepis pectinata ( Willd.) Schott.

Illustration.Maciel (2016MACIEL, S. 2016. Nephrolepis (Lomariopsidaceae - Polypodiopsida) na Amazônia brasileira. Rodriguésia 67(1): 77-84.: 80, fig. 1h-k).

Epiphytic in the upper part of a babaçu palm in an area of pasture. Habitat: anthropogenic area. Geographic distribution: AC, AM, AP, PA, BA, MA, PE, MT (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Serpocaulon triseriale (Sw.) A.R.Sm.

(Figure 6C).

Terrestrial on a non-rocky bank near an area with buriti palms and rupicolous plant collected on a rocky bank. Habitat: open riparian forest. Geographic distribution: AC, AM, PA, TO, AL, BA, CE, MA, PE, DF, GO, MS, MT, ES, MG, RJ, SP, PR, RS, SC. (Amazonia, Caatinga, Cerrado, Atlantic Forest, Pampa and Pantanal). New record: Maranhão.

Adiantum intermedium Sw.

(Figure 7A)

Figure 7
Habit. A. Adiantum intermedium Sw. B. Adiantum latifolium Lam. C. Adiantum serratodentatum Willd. D. Adiantum terminatum Kunze ex Miq. E. Cheilanthes pohliana Mett. F. Vittaria lineata (L.) Sm. G. Azolla microphylla Kaulf.

Rupicolous on a rocky bank and terrestrial plant collected on a non-rocky bank in a waterfall area. Habitat: closed riparian forest. Geographic distribution: MA, DF, GO, MS, MT, MG, RJ, SP, PR, SC (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Adiantum tetraphyllum Humb. Bonpl. ex Willd..

Illustration. Prado et al. (2017PRADO, J., HIRAI, R.Y., MORAN, C. R. 2017. Fern and lycophyte flora of Acre state, Brazil Biota Neotrop. 17(4): 1-59.: 45, fig. 46E, F).

Terrestrial in capoeira in terra firme forest near a watercourse. Habitat: closed riparian forest. Geographic distribution: AC, AM, AP, PA, RO, RR, TO, BA, CE, MA, PE, DF, GO, MS, MT, ES, MG, RJ, SP, PR, SC (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Azolla microphylla Kaulf..

(Figure 7G)

Floating aquatic in open flooded area above a waterfall. Habitat: open riparian forest. Geographic distribution: AM, BA, CE, MA, PE, SE, MG, PR, SC. (Amazonia, Caatinga, Cerrado and Atlantic Forest). New record: Cerrado.

Schizaea incurvata Schkuhr.

Terrestrial on a non-rocky bank inside a forest in a flat area with litter. Habitat: Cerrado sensu stricto. Geographic distribution: AM, AP, PA, RO, MA (Amazonia and Cerrado). New record: Northeast Region and Cerrado.

Tectaria incisa Cav.

(Figure 8A)

Figure 8
A. Tectaria incisa Cav. Habit. B-C. Christella conspersa (Schrad.) Á.Löve & D.Löve. B.| Habit. C. Detail of fertile pinnae showing a sori. D. Goniopteris biformata (Rosenst) Salino & T.E. Almeida. Habit. E. Meniscium chrysodioides Fée. Habit. F-G. Meniscium delicatum R.S. Fernandes & Salino. F. Habit. G. Detail of fertile pinnae showing a sori and anastomosing veins. H-I. Meniscium hostmannii (Klotzsch) R.S. Fernandes & Salino. H. Habit. I. Detail of fertile pinnae showing a sori.

Rupicolous on a rocky bank in a waterfall area. Habitat: closed riparian forest. Geographic distribution: AC, AM, AP, PA, RO, RR, AL, BA, CE, MA, PE, MS, MT, ES, MG, RJ, SP, PR, RS, SC (Amazonia, Cerrado and Atlantic Forest). New record: Cerrado.

Goniopteris biformata (Rosenst) Salino & T.E. Almeida

(Figure 8D)

Terrestrial on the margin of a waterfall and rupicolous plant collected on a rock wall. Habitat: open riparian forest. Geographic distribution: AC, PA, GO, MS, MT, MG, SP (Amazonia, Cerrado and Atlantic Forest). New record: Cerrado.

Macrothelypteris torresiana (Gaudich.) Ching.

Illustration.Smith (1992SMITH, A.R. 1992. Thelypteridaceae. In: Tryon, R.M. & Stolze, R.G. (Eds.) Pteridophyta of Peru. Part III. Fieldiana Botany 29: 1-80.: 4, fig. 1a-d).

Rupicolous on a rock wall near a waterfall. Habitat: closed riparian forest. Geographic distribution: RO, AL, BA, CE, MA, PB, PE, RN, DF, GO, MS, MT, ES, MG, RJ, SP, PR, RS, SC (Cerrado, Atlantic Forest and Pampa). New record: Maranhão.

Meniscium chrysodioides Fée.

(Figure 8E)

Terrestrial on a non-rocky bank, in a marshy area with buriti palms, and rupicolous plant collected on a rock wall in a waterfall area. Habitat: open riparian forest; closed riparian forest. Geographic distribution: AC, PA, AL, MA, PE, GO, MS, MG, SP (Amazonia, Cerrado and Atlantic Forest). New record: Maranhão.

Discussion

Based on the present study, PNCM is the area (protected or not) with the greatest diversity of ferns and lycophytes (86 species) in Maranhão State. Mirador State Park is another protected area of Cerrado in the state. Despite its large size (450,838 hectares), only seven species of lycophytes and ferns have been recorded in the area (Conceição & Rodrigues 2010CONCEIÇÃO, G.M. & RODRIGUES, M.S. 2010. Pteridófitas do Parque Estadual do Mirador, Maranhão, Brasil. Cad. Geociênc. (7): 47-53.). However, this low diversity could be related to insufficient sampling, since it is a preserved area of Cerrado that probably has a diversity similar to PNCM. The Cerrado in Maranhão is strongly influenced by other domains (e.g., Amazonia and Caatinga) that, in general, favors a higher diversity of plant species (e.g., Ribeiro et al. 2020RIBEIRO, R.T.M., REBOUÇAS, N.C., LOIOLA, M.I.B., SALES, M.F. 2020. Terminalia s.s. (Combretaceae) in Maranhão state, Brazil. Rodriguésia [online]. 2020, v. 71, e00942019. Available in: <https://doi.org/10.1590/2175-7860202071121>. Epub 23 Nov 2020. ISSN 2175-7860. https://doi.org/10.1590/2175-7860202071121 (last access 14/07/2021).
https://doi.org/10.1590/2175-78602020711...
, Silva et al. 2021SILVA, J.P, OLIVEIRA-DA-SILVA, F.R, ILKIU-BORGESAL & FERNANDES, R.S. 2021. Leafy liverworts of Chapada das Mesas National Park: a floristic survey and checklist of the leafy liverworts of Maranhão state, Brazil. Check List 17 (2): 479-495., Fernandes et al. 2021FERNANDES, R.S., SILVA, J.A.S., OTTONI, F.P. & COSTA, D.P. 2021. Diversity of thalloid liverworts in Brazilian Savanna of Parque Nacional da Chapada das Mesas, Maranhão, Brazil. Check List 17(1): 45-58.).

The species collected in the present study represent around 27.30% of the species recorded for the Brazilian Cerrado and increase the known diversity in this domain by 11 species that, until now, were only recorded for Amazonia and the Atlantic Forest (Flora do Brasil 2020FLORA DO BRASIL 2020. Jardim Botânico do Rio de Janeiro. Available in: < http://floradobrasil.jbrj.gov.br/ >. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/...
). Additionally, this inventory resulted in 26 new records for Maranhão and five new records for the Northeast Region of Brazil. This shows the importance of this protected area for the conservation of the species of the groups studied. The number of new records in this study is probably a reflection of low sampling and local inventories (e.g., Fernandes et al. 2007FERNANDES, R.S., CONCEIÇÃO, G.M., BRITO E.S. & PAULA-ZÁRATE, E.L. 2007. Diversidade Florística de Pteridófitas da Área de Preservação Ambiental do Inhamum, Caxias, Maranhão, Brasil. Rev. bras. Bioci. 5(2): 411-413., Conceição & Ruggieri 2010CONCEIÇÃO, G.M. & RUGGIERI, A.C. 2010. Pteridófitas do município de Tufilândia, Estado do Maranhão, Brasil. Pesquisa em Foco. 18(1): 59-68., Conceição & Rodrigues 2010CONCEIÇÃO, G.M. & RODRIGUES, M.S. 2010. Pteridófitas do Parque Estadual do Mirador, Maranhão, Brasil. Cad. Geociênc. (7): 47-53., Fernandes et al. 2010FERNANDES, R.S., CONCEICÃO, G.M., COSTA J.M. & PAULA-ZÁRATE, E.L. 2010. Samambaias e licófitas do município de Caxias, Maranhão, Brasil. Bol. Mus. Emílio Goeldi. Ciênc. Nat. (3): 345-356., Conceição et al. 2015CONCEIÇÃO, G.M., PAULA-ZARATE, E.L., RUGGIERI, A.C., SILVA, E.O. & SILVA, M.F. 2015. Pteridoflora e seus aspectos ecológicos no município de Timon, Maranhão, Brasil. Braz. Geogr. J. 6(1): 74-81., Silva et al. 2017SILVA, G.S., SILVA, D.L.S., OLIVEIRA, R.R., SILVA, M.L.A. & CONCEIÇÃO, G.M. 2017. Licófitas e samambaias no cerrado do leste do Maranhão, Brasil. Acta Bra. 1(2): 13-16., Silva Júnior et al. 2018) that underestimated the diversity of lycophytes and ferns in the state.

The fern family with the most species is Pteridaceae (14 species). This can be explained by the wide distribution of the family in tropical regions and arid regions (Smith et al. 2006SMITH AR, PRYER KM, SCHUETTPELZ E, KORALL P, SCHNEIDER H, WOLF PG. 2006. A classification for extant ferns. Taxon 55: 705-731.), and due to in Brazil the family is most diverse in Southeast (141 spp) and Northeast (104 spp) regions (Prado et al. 2020PRADO, J., SMITH-BRAGA, N., HIRAI, R.Y., DITTRICH, V.A.O., LINK-PEREZ, M., SCHUETTPELZ, E., DELLA, A.P., SCHWARTSBURD, P.B., LIMA, L.V., GASPER, A.L., PONCE, M.M., OLIVEIRA, A.G.S., MIRANDA, C.V., PENA, N.T.L. 2020. Pteridaceae in Flora do Brasil 2020. Jardim Botânico do Rio de Janeiro. Available in: <http://floradobrasil.jbrj.gov.br/reflora/floradobrasil/FB91793>. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/reflora...
). Other studies in Cerrado (e.g., Fernandes et al. 2007FERNANDES, R.S., CONCEIÇÃO, G.M., BRITO E.S. & PAULA-ZÁRATE, E.L. 2007. Diversidade Florística de Pteridófitas da Área de Preservação Ambiental do Inhamum, Caxias, Maranhão, Brasil. Rev. bras. Bioci. 5(2): 411-413., 2010FERNANDES, R.S., CONCEICÃO, G.M., COSTA J.M. & PAULA-ZÁRATE, E.L. 2010. Samambaias e licófitas do município de Caxias, Maranhão, Brasil. Bol. Mus. Emílio Goeldi. Ciênc. Nat. (3): 345-356., Silva et al. 2017SILVA, G.S., SILVA, D.L.S., OLIVEIRA, R.R., SILVA, M.L.A. & CONCEIÇÃO, G.M. 2017. Licófitas e samambaias no cerrado do leste do Maranhão, Brasil. Acta Bra. 1(2): 13-16.) and Amazonia (e.g., Silva Junior et al. 2020) in Maranhão State also recorded more diversity for this family. In PNCM, 10 of the 14 Pteridaceae species recorded prefer a rocky substrate (Table 1). Adiantum L. (Pteridaceae) had the highest number of recorded species (10 species), of which two are new records for Maranhão (Adiantum intermedium Sw. and A. tetraphyllum Humb. & Bonpl. ex Willd.) and one (A. petiolatum Desv.) is a new record for the Brazilian Cerrado (Prado et al. 2020PRADO, J., SMITH-BRAGA, N., HIRAI, R.Y., DITTRICH, V.A.O., LINK-PEREZ, M., SCHUETTPELZ, E., DELLA, A.P., SCHWARTSBURD, P.B., LIMA, L.V., GASPER, A.L., PONCE, M.M., OLIVEIRA, A.G.S., MIRANDA, C.V., PENA, N.T.L. 2020. Pteridaceae in Flora do Brasil 2020. Jardim Botânico do Rio de Janeiro. Available in: <http://floradobrasil.jbrj.gov.br/reflora/floradobrasil/FB91793>. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/reflora...
, Silva Junior et al. 2020).

The second most representative fern family is Thelypteridaceae with 11 species, of which three are reported for the first time for Maranhão State (Goniopteris biformata (Rosenst) Salino & T.E. Almeida, Macrothelypteris torresiana (Gaudich.) Ching, and Meniscium chrysodioides Fée); Goniopteris biformata is also a new record for the Northeast Region of Brazil (Fernandes & Salino 2020FERNANDES, R.S. & SALINO, A. 2020. Taxonomic revision of Meniscium Schreber (Thelypteridaceae: Polypodiopsida). Phytotaxa 463(1): 1-127., Salino et al. 2020SALINO, A., FERNANDES, R.S., MOURA, I.O., MOURA, L.C., ALMEIDA, T.E., PAIXÃO, L.C. 2020. Thelypteridaceae in Flora do Brasil 2020. Jardim Botânico do Rio de Janeiro. Available in: <http://floradobrasil.jbrj.gov.br/reflora/floradobrasil/FB92151>. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/reflora...
).

The diversity of lycophytes (17 species) in PNCM is high compared to other areas sampled in the state (e.g., Fernandes et al. 2007FERNANDES, R.S., CONCEIÇÃO, G.M., BRITO E.S. & PAULA-ZÁRATE, E.L. 2007. Diversidade Florística de Pteridófitas da Área de Preservação Ambiental do Inhamum, Caxias, Maranhão, Brasil. Rev. bras. Bioci. 5(2): 411-413., 2010FERNANDES, R.S., CONCEICÃO, G.M., COSTA J.M. & PAULA-ZÁRATE, E.L. 2010. Samambaias e licófitas do município de Caxias, Maranhão, Brasil. Bol. Mus. Emílio Goeldi. Ciênc. Nat. (3): 345-356., Conceição & Rodrigues 2010CONCEIÇÃO, G.M. & RODRIGUES, M.S. 2010. Pteridófitas do Parque Estadual do Mirador, Maranhão, Brasil. Cad. Geociênc. (7): 47-53.). In Amazonia in Maranhão, for example, only two species of lycophytes have been recorded (Silva Junior et al. 2020), which is nine times less than that in PNCM. The lycophyte family with the most species is Selaginellaceae (12 species), of which three are reported for the first time for Maranhão State (Selaginella convoluta (Arn.) Spring, Selaginella minima Spring, and Selaginella sulcata (Desv. ex Poir.) Spring ex Mart.); the last one is also a new record for the Northeast Region of Brazil (Góes-Neto et al. 2020GÓES-NETO, L.A.A., BARCELLOS, I., SPINELI, G., SALINO, A. 2020. Selaginellaceae in Flora do Brasil 2020. Jardim Botânico do Rio de Janeiro. Available in: <http://floradobrasil.jbrj.gov.br/reflora/floradobrasil/FB92047>. (last access 19/11/2021).
http://floradobrasil.jbrj.gov.br/reflora...
). Compared to Amazonia in Maranhão (Silva Junior et al. 2020), the high diversity of Selaginellaceae recorded in our study is due to the predominance of rupicolous habitats associated with waterfalls in PNCM (nine rupiculous species, Table 2).

The predominance of rupicolous species (22 species) in the present study was expected and is probably due to the wide availability of rock substrates in PNCM, such as rock walls of waterfalls and surroundings, and extensive rocky fragments inside riparian forest. Since there is a lot of rock substrate, species that are normally epiphytic (e.g., Didymoglossum angustifrons Fée) or terrestrial (e.g., Trichomanes hostmannianum) (Costa & Pietrobom 2007COSTA, J.M. & PIETROBOM, M.R. 2007. Pteridófitas (Lycophyta e Monilophyta) da Ilha de Mosqueiro, município de Belém, estado do Pará, Brasil. Bol. Mus. Para. Emílio Goeldi. 2(3):45-55.) in the study area develop on rocks. The second most recorded habit was terrestrial (15 species). A high number of terrestrial species is common in most studies about ferns in Maranhão State, for example, Bastos & Cutrim (1999)BASTOS, C.C.C. & CUTRIM, M.V.J. 1999. Pteridoflora da Reserva florestal do Sacavém, São Luis - Maranhão. Bol. Mus. Para. Emílio Goeldi, sér. Bot. 15(1): 3-37., Fernandes et al. (2007)FERNANDES, R.S., CONCEIÇÃO, G.M., BRITO E.S. & PAULA-ZÁRATE, E.L. 2007. Diversidade Florística de Pteridófitas da Área de Preservação Ambiental do Inhamum, Caxias, Maranhão, Brasil. Rev. bras. Bioci. 5(2): 411-413., Fernandes et al. (2010)FERNANDES, R.S., CONCEICÃO, G.M., COSTA J.M. & PAULA-ZÁRATE, E.L. 2010. Samambaias e licófitas do município de Caxias, Maranhão, Brasil. Bol. Mus. Emílio Goeldi. Ciênc. Nat. (3): 345-356., Conceição & Ruggieri (2010)CONCEIÇÃO, G.M. & RUGGIERI, A.C. 2010. Pteridófitas do município de Tufilândia, Estado do Maranhão, Brasil. Pesquisa em Foco. 18(1): 59-68., Conceição & Rodrigues (2010)CONCEIÇÃO, G.M. & RODRIGUES, M.S. 2010. Pteridófitas do Parque Estadual do Mirador, Maranhão, Brasil. Cad. Geociênc. (7): 47-53., Conceição et al. (2015)CONCEIÇÃO, G.M., PAULA-ZARATE, E.L., RUGGIERI, A.C., SILVA, E.O. & SILVA, M.F. 2015. Pteridoflora e seus aspectos ecológicos no município de Timon, Maranhão, Brasil. Braz. Geogr. J. 6(1): 74-81., Silva et al. (2017)SILVA, G.S., SILVA, D.L.S., OLIVEIRA, R.R., SILVA, M.L.A. & CONCEIÇÃO, G.M. 2017. Licófitas e samambaias no cerrado do leste do Maranhão, Brasil. Acta Bra. 1(2): 13-16., and Silva Junior et al. (2020).

In relation to environment type, most fern and lycophyte species generally occur in microhabitats in riparian forest, such as rocky banks, non-rocky banks, rock walls, waterfall areas and marshy areas (Table 2 and Supplementary file 1). Some species of Schizaeaceae (e.g., Actinostachys pennula (Sw.) Hook., Schizaea incurvata Schkuhr) and Anemiaceae (e.g., Anemia elegans (Gardner) C.Presl, A. trichorhiza Gardner) were collected in Cerrado sensu stricto (Table 1) in distinct microhabitats (inside forest in flat area and rock wall, respectively) (Table 2).

Conclusion

The present work shows that the fern and lycophyte diversity in the Cerrado in Maranhão is underestimated. This is mainly due to low sampling in previous studies, or a low number of sampling points (locations), and because the collections in Maranhão herbaria do not properly represent these groups. Based on this study, we encourage others to conduct similar studies that collect a lot of material and deposit specimens in herbaria that are open to the public. Overall, this will contribute to a more accurate estimate of the diversity of ferns and lycophytes in the Cerrado in Maranhão.

Acknowledgments

We thank the specialists Dr. Luiz Armando de Araújo Góes-Neto, Dr. Jovani Bernardino de Sousa Pereira, Dr. Pedro Bond Schwartsburd, Dr. Jefferson Prado, Vinícius Antonio de Oliveira Dittrich and Dr. Alexandre Salino for examining the specimens and confirming the identification of some species of the genus Selaginella, Isoëtes, Pteridium, Adiantum, Blechnum, Christella and Goniopteris. We also thank Msc. José Augusto dos Santos Silva and Dr. Fredgarson Costa Martins for helping to collect the material. This project was financially supported by FAPEMA, Fundação de Amparo em Pesquisa do Estado do Maranhão (Processo universal nº 01271/2016).

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Edited by

Associate Editor
Carlos Joly

Publication Dates

  • Publication in this collection
    21 Jan 2022
  • Date of issue
    2022

History

  • Received
    21 Aug 2021
  • Accepted
    28 Nov 2021
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