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Flora of Paraíba, Brazil: Bombacoideae Burnett (Malvaceae)

Flora da Paraíba, Brasil: Bombacoideae Burnett (Malvaceae)

Abstract:

This work presents the taxonomic study of the native species of Bombacoideae Burnett (Malvaceae) in the state of Paraíba, Northeastern Brazil. The taxonomic treatment included keys for identifying genera and species, morphological descriptions, diagnostic illustrations, comments on taxonomic affinities, and additional information on geographical distribution, habitat, and flowering and fruiting of the species. Three genera and six species were recorded: Ceiba Mill., represented by C. glaziovii (Kuntze) K. Schum., is a new record for the Atlantic Forest; Eriotheca Schott & Endl., represented by E. gracilipes (K. Schum.) A. Robyns and E. macrophylla (K. Schum.) A. Robyns, is a new record for Paraíba; and Pseudobombax Dugand, which is represented by P. marginatum (A.St.-Hil., Juss. & Cambess.) A. Robyns, P. parvifolium Carv.-Sobr. & L.P. Queiroz and P. simplicifolium A. Robyns Robyns - the last one registered for the first time in Paraíba in this study.

Keywords:
conservation; diversity; endemism; Northeastern, Brazil; taxonomy

Resumo:

Este trabalho apresenta o estudo taxonômico das espécies de Bombacoideae Burnett (Malvaceae) nativas para a Paraíba, nordeste brasileiro. O tratamento taxonômico incluiu chaves para identificação de gêneros e espécies, além de descrições morfológicas, ilustrações dos caracteres diagnósticos, comentários sobre afinidades taxonômicas, dados de distribuição geográfica, habitats, floração e frutificação das espécies. Foram registrados três gêneros e seis espécies: Ceiba Mill., está representado por C. glaziovii (Kuntze) K. Schum. e constitui um novo registro para a Mata Atlântica; Eriotheca Schott & Endl. consiste em um novo registro para a Paraíba, representado por duas espécies: E. gracilipes (K. Schum.) A. Robyns e E. macrophylla (K. Schum.) A. Robyns; e Pseudobombax Dugand, com três espécies: P. marginatum (A.St.-Hil., Juss. & Cambess.) A. Robyns, P. parvifolium Carv.-Sobr. & L.P. Queiroz e P. simplicifolium A. Robyns, essa última sendo registrada pela primeira vez para o Estado nesse estudo.

Palavras-chave:
conservação; diversidade; endemismo; Nordeste, brasileiro; taxonomia

Introduction

Malvaceae Juss. includes about 250 genera and 4,200 species, showing predominantly a pantropical distribution (Judd et al. 2009JUDD, W.S., CAMPBELL, C.S., KELLOG, E.A., STEVENS, P. & DONOGHUE, M.J. 2009. Sistemática Vegetal - Um enfoque filogenético. 3ª ed. Porto Alegre: Artmed.). Morphologically, this family is primarily characterized by presenting a nectariferous tissue located at the base of the calyx (or, less often, of the petals or sepals), valvular androgynophore, mucilage channels, and leaves with primary palminervate venation (Judd & Manchester 1997JUDD, W.S. & MANCHESTER, S.R. 1997. Circumscription of Malvaceae (Malvales) as determined by a preliminary cladistics’ analysis of morphological, anatomical, palynological, and chemical characters. Brittonia 49:384-405., Judd et al. 1999JUDD, W.S., CAMPBELL, C.S., KELLOGG, E.A. & STEVENS, P.F. 1999. Plant systematics. A Phylogenetic approach. Sunderland: Sinauer Associates.).

Bombacaceae, formally known as Bombacoideae in phylogenetic classification systems, is now inserted in Malvaceae sensu lato (s.l.) as one of its nine monophyletic subfamilies, corroborated the studies of Baum et al. (1998)BAUM, D.A., ALVERSON, W.S. & NYFFELER, R. 1998. A durian by any other name: Taxonomy and nomenclature of the core Malvales. Harv. Pap. Bot. 3: 315-330., APG I (1998) APG. 1998. An ordinal classification for the families of flowering plants. Ann. Mo. Bot. Gard. 85: 531-553., Alverson et al. (1999)ALVERSON, W.S., WHITLOCK, B.A., NYFFELER, R., BAYER, C. & BAUM, D.A. 1999. Phylogeny of the core Malvales: evidence from ndhf sequence data. Am. J. Bot. 86(10):1474-1486. and APG IV (2016)APG IV. 2016. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Bot. J. Linn. Soc. 181:1-20..

Bombacoideae gathers approximately 18 genera and 187 species, most of them pantropical with a greater diversity of species in the rainforests of South America. Brazil and Colombia are the more prominent countries for their highest representativeness in relation to the number of species (Gibbs & Semir 2003GIBBS, P. & SEMIR, J. 2003. A Taxonomic revision of the genus Ceiba Mill. (Bombacaceae). Anales del Jardín Botánico de Madrid. Consejo Superior de Investigaciones Científicas.). According to the BFG (2015)BFG - The Brazil Flora Group. 2015. Growing knowledge: an overview of seed plant diversity in Brazil. Rodriguésia 66(4):1085-1113., 13 genera and about 80 species can be found in Brazil, mainly in the North and Northeast regions of the country.

Their species of Bombacoideae usually present deciduous leaves, with sessile or petiolate leaflets; often large flowers with sepals generally concrescent and glandular trichomes at the base; the receptacle is usually glandular; the ovary is superolateral, and the fruits, to the vast majority of their representatives, are capsule opening for 3-5 valves, with plentiful silky fibers and generally oilseeds inside (Reyes 1998REYES, S.A. 1998. Bombacaceae. In Flora de Veracruz. Instituto de Ecología, A. C. Xalapa, Veracruz, México. p. 3-40., Bocage-Neta & Sales 2002BOCAGE-NETA, A.L. & SALES, M.F. 2002. A família Bombacaceae Kunth no Estado de Pernambuco, Brasil. Acta Bot. Bras. 169:123-139., Aguiar 2012AGUIAR, C. 2012. Botânica para Ciências Agrárias e do Ambiente. Sistemática. Instituto Politécnico de Bragança 3:1-81.).

In general, the representatives of Bombacoideae have great economic importance and the can be used for various purposes: the wood can be used for manufacturing small boats, furniture, light objects, and cellulose paste; the wool that surrounds the seeds can be used for making life jackets, filling mattresses, pillows and as a thermal insulator; some seeds can be edible; in the ornamentation of squares (Esteves 2005ESTEVES, G.L. 2005. Flora da Reserva Ducke, Amazonas, Brasil: Bombacaceae. Rodriguésia 56:115-124., Lorenzi 2002aLORENZI, H. 2002a. Árvores brasileiras. Manual de identificação e cultivo de plantas arbóreas nativas do Brasil. 1ª ed. Nova Odessa: Instituto Plantarum. p. 352., Lorenzi 2002bLORENZI, H. 2002b. Árvores brasileiras. Manual de identificação e cultivo de plantas arbóreas nativas do Brasil. 2ª ed. Nova Odessa: Instituto Plantarum. p. 352.). Their representatives can also used in the reforestation of degraded areas as they are considered to be rapidly growing (Lorenzi 2002aLORENZI, H. 2002a. Árvores brasileiras. Manual de identificação e cultivo de plantas arbóreas nativas do Brasil. 1ª ed. Nova Odessa: Instituto Plantarum. p. 352., Lorenzi 2002bLORENZI, H. 2002b. Árvores brasileiras. Manual de identificação e cultivo de plantas arbóreas nativas do Brasil. 2ª ed. Nova Odessa: Instituto Plantarum. p. 352.).

Considering the representativeness of Bombacoideae in Brazil and the scarcity of studies in the Northeast region (e.g., Gibbs & Semir 2003GIBBS, P. & SEMIR, J. 2003. A Taxonomic revision of the genus Ceiba Mill. (Bombacaceae). Anales del Jardín Botánico de Madrid. Consejo Superior de Investigaciones Científicas., Esteves 2005ESTEVES, G.L. 2005. Flora da Reserva Ducke, Amazonas, Brasil: Bombacaceae. Rodriguésia 56:115-124., Carvalho-Sobrinho & Queiroz 2008CARVALHO-SOBRINHO, J.G. & QUEIROZ, L.P. 2008. Ceiba rubriflora (Malvaceae: Bombacoideae), a new species from Bahia, Brazil. Kew Bull. 63:649-653., Carvalho-Sobrinho & Queiroz 2010CARVALHO-SOBRINHO, J.G. & QUEIROZ, L. P. 2010. Three new species of Pseudobombax (Malvaceae, Bombacoideae) from Brazil. Novon 20:13-20., Duarte 2010DUARTE, M.C. 2010. Análise filogenética de Eriotheca Schott & Endl. e gêneros afins (Bombacoideae, Malvaceae) e estudo taxonômico de Eriotheca no Brasil. Tese de Doutorado, Instituto de Botânica da Secretaria de Estado do Meio Ambiente, São Paulo., Duarte et al. 2011DUARTE, M.C., ESTEVES, G.L., SALATINO, M.L.F., WALSH, K.C. & BAUM, D.A. 2011. Phylogenetic analyses of Eriotheca and related genera (Bombacoideae, Malvaceae). Systematic Botany. 36:690-701., Carvalho-Sobrinho 2013CARVALHO-SOBRINHO, J.G. 2013. A new species of Eriotheca (Malvaceae: Bombacoideae) from Espírito Santo, Eastern Brazil. Phytotaxa 108:49-53.), the objective of this work was to elaborate taxonomic study of this subfamily in the state of Paraíba in order to enlarge the knowledge on its richness and geographical distribution. Identification keys genera and species, morphological descriptions and illustrations, data on geographic distribution and preferred environments, in addition to the phenology of the species found in the study area are presented.

Material and Methods

1. Study area

The State of Paraíba (Figure 1) is located in the Northeast of Brazil and includes 223 municipalities. It presents a territorial extension of 56,469.744 km ² divided into four meso-regions: Zona da Mata, Agreste, Borborema and hinterland (IBGE 2018IBGE - PARAÍBA. 2018. Fundação Instituto Brasileiro de Geografia e Estatística. http://www.ibge.gov.br/estadosat/perfil.php?sigla=pb (last access on 26/05/2019).
http://www.ibge.gov.br/estadosat/perfil....
). Its vegetation consists of mangroves (on the coast), a small strip of rainforest (Mata Atlântica) that stretches along the coast and enters to the West, forming projections associated with humid areas (elevated wetlands, Caatinga) and, in most parts, the Caatinga that comprises about 80% of the territory in which the vegetation vary between closed bushy-arboreal to closed arboreal caatinga (Figure 2) (Paraíba 2018PARAÍBA. 2018. Secretaria de Estado da Ciência e Tecnologia e do Meio Ambiente. Agência Executiva de Gestão de Águas do Estado da Paraíba, AESA. PERH-PB: Plano Estadual de Recursos Hídricos: Resumo Executivo e Atlas, Brasília., Portal Brasil 2018PORTAL BRASIL. 2018. Estados Brasileiros - Paraíba. http://www.portalbrasil. net/estados_rn.htm (last access on 26/05/2019).
http://www.portalbrasil. net/estados_rn....
).

Figure 1
Location of the study area, State of Paraíba, Northeastern Brazil (Map: Rodrigues, E.M. 2017).

Figure 2
Preferred environments of the Bombacoideae species (Malvaceae) found in the State of Paraíba: a. APA do Cariri, Boa Vista; b. Outcrop in Puxinanã; c. Serra of the ABA, Passagem; d. Serra Branca; e. Roncador Falls, Bananeiras; f. Do Pinga Waterfalls, Lagoa Seca (Photos: A-C. Costa, S.L.; B. H. Crisóstomo; D-E. Monteiro, F.K.S.; F. Sousa, T.S.).

2. Collecting expeditions and preservation

Monthly expeditions from August/2016 to February/2018 were made to several municipalities of Paraíba, covering areas of the Caatinga and the Atlantic Rainforest vegetation. Vegetative samples (stems and leaves) and fertile specimens (with flowers and/or fruit) of Bombacoideae representatives were collected. These samples were herborized and/or fixed in alcohol (70%) for detailed posterior morphological analyses, according to Peixoto & Maia (2013)PEIXOTO, A.L. & MAIA, L.C. (Orgs.). 2013. Manual de Procedimentos para Herbários. INCT-Herbário Virtual para a Flora e os Fungos. Editora Universitária, UFPE, Recife.. These analyses were made in the laboratory of Botany and the specimens were incorporated into the collection of the Herbarium Manuel de Arruda Câmara (HACAM), both of the Department of Biology, Campus I, of the State University of Paraíba (UEPB).

3.Taxonomic study

Morpho-taxonomic analyses were carried out between September/2016 and February/2018. During this stage, vegetative and reproductive structures were examined and resulted in the indentification of genera and species.

The identifications were based on the bibliography of Bombacaceae, Bombacoideae and Malvaceae s.l. specially the studies of: Reyes (1998)REYES, S.A. 1998. Bombacaceae. In Flora de Veracruz. Instituto de Ecología, A. C. Xalapa, Veracruz, México. p. 3-40., Bocage-Neta & Sales (2002)BOCAGE-NETA, A.L. & SALES, M.F. 2002. A família Bombacaceae Kunth no Estado de Pernambuco, Brasil. Acta Bot. Bras. 169:123-139., Gibbs & Semir (2003)GIBBS, P. & SEMIR, J. 2003. A Taxonomic revision of the genus Ceiba Mill. (Bombacaceae). Anales del Jardín Botánico de Madrid. Consejo Superior de Investigaciones Científicas., Carvalho-Sobrinho & Queiroz (2008)CARVALHO-SOBRINHO, J.G. 2013. A new species of Eriotheca (Malvaceae: Bombacoideae) from Espírito Santo, Eastern Brazil. Phytotaxa 108:49-53., Esteves (2005)ESTEVES, G.L. 2005. Flora da Reserva Ducke, Amazonas, Brasil: Bombacaceae. Rodriguésia 56:115-124., Carvalho-Sobrinho & Queiroz (2010)CARVALHO-SOBRINHO, J.G. & QUEIROZ, L. P. 2010. Three new species of Pseudobombax (Malvaceae, Bombacoideae) from Brazil. Novon 20:13-20. and Carvalho-Sobrinho (2013)CARVALHO-SOBRINHO, J.G. 2013. A new species of Eriotheca (Malvaceae: Bombacoideae) from Espírito Santo, Eastern Brazil. Phytotaxa 108:49-53.. In addition, classical literature about the group was also consulted: De Candolle (1824)DE CANDOLLE, A.P. 1824. Bombaceae. In Prodromus systematis naturalis reagni vegetabilis. París: victoris Masson et Filili, vol.5. Pp. 475-480.; Bentham & Höoker (1862)BENTHAM, G. & HOOKER, J.D. 1862. Bombacaceae. In Genera Plantarum, London: L. Reeve & Co. vol.1. Pp. 209-213. and Schumann (1886)SCHUMANN, K. 1886. Bombaceae. In K.F.P. Von Martius, A.G. Eichler & I. Urban (eds.). Flora Brasiliensis 12:201-250.. The collections available on SpeciesLink, Tropics (www.tropicos.org) and Virtual Herbarium of Flora and fungos (Reflora) were also examined.

For morphological descriptions, specimens (vouchers) from the herbaria of Paraíba (CSTR, EAN, HACAM and JPB), Pernambuco (IPA and PEUFR) and Rio de Janeiro (RB), complemented by its own collections were used. Due to the lack of diagnostic structures such as flowers and fruits, the descriptions of some taxa were also based on additional specimens. The diagnosis of Eriotheca gracilipes, E. macrophylla and Pseudobombax simplicifolium were complemented by plant specimens from the online collections of herbaria online CEPEC, JPB and RB. Approximately 800 samples were analyzed from both physical holdings and scanning-based materials (Reflora). The herbaria acronyms follow Thiers et al. (continuously updated)THIERS, B. [continuously updated]. Index Herbariorum: A global directory of public herbaria and associated staff. New York Botanical Garden’s Virtual Herbarium. http://sweetgum.nybg.org/ih/ (last access on 26/05/2019).
http://sweetgum.nybg.org/ih/...
.

The following specific terminologies were adopted: foliar typification (Rizzini 1977RIZZINI, C.T. 1977. Sistematização terminológica da folha. Rodriguésia 42:103-125.), venation patterns (Hickey 1973HICKEY, L.J. 1973. Classification of the Architecture of Dicotyledonous Leaves. Am. J. Bot. 60:17-33.), indument (Payne 1978PAYNE, W.W. 1978. A Glossary of plant hair terminology. Brittonia 30:239-255.). In general, for the description of vegetative and reproductive structures, Hickey & King (2000)HICKEY, M. & KING, C. 2000.The Cambridge Illustrated Glossary of Botanical Terms. was followed.

An identification key and illustrations of the main diagnostic charactres were prepared. The taxonomic treatment includes morphological descriptions, illustrations in Nankin ink and images of species and environments, the period of flowering and fruiting (phenology), geographic distribution, preferred environments and taxonomic, and taxonomic comments.

Results and Discussion

1. Taxonomic Treatment

Bombacoideae Burnett

Bombacoideae is characterized by the leaves usually deciduous, petiolate, alternate, simple or composed, scanned with sessile or petiolate, articulate or inarticulate leaflets (Bocage-Neta & Sales 2002BOCAGE-NETA, A.L. & SALES, M.F. 2002. A família Bombacaceae Kunth no Estado de Pernambuco, Brasil. Acta Bot. Bras. 169:123-139.). The flowers are often bracteolate, large, hermaphroditic, actinomorphous, rarely more or less zigomorphous, usually pentamerous; sepals free or concrescent with glandular trichomes on the base; the receptacle generally glandular. Calyx usually campanulate; petals 5, usually adnate to the base of the stem tube; 5-numerous stamens usually monadelphous or poliadelphous, epipetalous; 1-thecae to numerous thecae, pistil 2-5 (10) -carpels, sincarpic, upper ovary, sometimes semi-infero, 2-10, 1-2 or locules with many ovule, capitate stigma. The fruit is usually the capsule type, smooth, sometimes prickly, fleshy, usually winged, opening for 3-5 valves, with plentiful silky fibers in its interior. The seeds are usually oilseeds (Reyes 1998REYES, S.A. 1998. Bombacaceae. In Flora de Veracruz. Instituto de Ecología, A. C. Xalapa, Veracruz, México. p. 3-40., Aguiar 2012AGUIAR, C. 2012. Botânica para Ciências Agrárias e do Ambiente. Sistemática. Instituto Politécnico de Bragança 3:1-81.).

In the study area, the subfamily is represented by three genera and six species. One genus (Eriotheca) and three species (E. gracilipes, E. macrophylla and Pseudobombax simplicifolium) represent new records for Paraíba.

Ceiba glaziovii had already been registered in areas of the Caatinga of the state of Paraíba, but, through this research, its istribution is now extended to areas of the Atlantic Forest.

Pseudobombax Dugand was the most representative genus, with three species [P. marginatum (A. St.-Hil., Juss. & Cambess.) A. Robyns, P. parvifolium Carv.-Sobr. & L.P. Queiroz and P. simplicifolium A. Robyns] all of them associated with the phytophysiognomy of Caatinga, followed by Eriotheca Schott & Endl., with two species (E. gracilipes and E. macrophylla), both associated with the Atlantic Forest (elevated wetlands), and Ceiba Mill., with the species C. glaziovii (Kuntze) K. Schum., associated with both the Caatinga and Atlantic Forest areas (elevated wetlands).

Key to the identification of species of Bombacoideae recorded in Paraíba, Brazil

  • 1. Stem aculeate with protuberance in the middle; stamens 5......................................................................................... 1.1. Ceiba glaziovii

  • 1. Stem unarmed; ; stamens more than 5.............................................. 2

  • 2. Lepidote leaflets; stamens constricted at the median portion until the base of the staminal tube ............................................................... 3

    • 3. Coriaceous leaflets; obovoid flower buds, calyx lepidote -brown externally .….………………………….............2.1. Eriotheca gracilipes

    • 3. Carthaceous leaflets; oblong flower buds, calyx floccose ferrugineous externall………………............................ 2.2. Eriotheca macrophylla

  • 2. Glabrescent to pubescent leaflets; stamens constricted only at the of the staminal tube.................................................................................. 4

    • 4. 3-leaflets leaves, united at the apex in braquiblasts (short stems) ………………………….……..….. 3.3. Pseudobombax simplicifolium

    • 4. 5-7 leaflets leaves, whitout braquiblasts (short stems)................... 5

  • 5. Stem rectilinear with dark green longitudinal streaks; seeds reniform ………………........................... 3.2. Pseudobombax parvifolium

    • 5. Irregular stem with greenish amorphous excrescences; seeds piriform………………………… 3.1. Pseudobombax marginatum

1. Ceiba Mill., Gard. Dict. Abr. (ed. 4): 287. 1754.

The genus includes 22 species, most of them restricted to seasonally dry forests of Brazil (Gibbs & Semir 2003GIBBS, P. & SEMIR, J. 2003. A Taxonomic revision of the genus Ceiba Mill. (Bombacaceae). Anales del Jardín Botánico de Madrid. Consejo Superior de Investigaciones Científicas.). In the Brazilian territory, Ceiba occurs from Mato Grosso do Sul to the northern Caatingas of the states of Minas Gerais and Bahia (Flora do Brasil 2020 in preparationFLORA DO BRASIL 2020 (in preparation). Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br (last access on 26/05/2019).
http://floradobrasil.jbrj.gov.br...
), almost always associated with rocky outcrops, rock fields, and limestone fields.

Morphologically, Ceiba can be characterized by presenting: robust and aculeate stems, with aculeous that propagating all over the branches, without longitudinal streaks, large canopy, leaves alternate, compound-digitate with long petioles, leaflets 5-7, with serrate margins; flowers solitary or in few-flowered inflorescences, pentamerous, diclamydeous, the outside surface of the petals covered with simple trichomes, stamens 5, anthers bithecae, stem tube with or without appendages. Capsule 5-valvate, with abundant wool, seeds numerous, subglobose, without streaks; hilum protruding (Gibbs & Semir 2003GIBBS, P. & SEMIR, J. 2003. A Taxonomic revision of the genus Ceiba Mill. (Bombacaceae). Anales del Jardín Botánico de Madrid. Consejo Superior de Investigaciones Científicas.). In the study area, Ceiba is represented by the species C. glaziovii, recorded in Caatinga vegetation (Agreste and Borborema).

1.1. Ceiba glaziovii (Kuntze) K. Schum., Bot. Jahresber. (Just) 26 (1): 343. 1900.

Trees, 14-15 m high; large canopy. Aculeate stem, including the young branches, with protuberance in the middle. Stipules absent. Compound leaves, digitate, 5-7 foliolated; petiole 80 mm long, 12.5 × 5 cm leaflets, oblanceolate, elliptical, membranaceous, acuminate apex, base cuneate to attenuated, entire margin from basis until the median region, serrate from median region until the apex, main vein salient on both sides propagating until the apex, glabrescent, secondary veins evident on both sides propagating until the apex, glabrescent, craspedodromous venation; solitary flowers, axillary, 8 cm long, scales absent, oblong and imbricate buds; pedicel 26 mm long; calyx 2.5 × 1.8 cm, campanulate, lobes 5, lightly apiculate, externally glabrous and internally with simple trichomes, nectariferous glands at the base of the receptacle; corolla 5.2 × 2.2 cm, spatulate, obovate apex, white, lilac to pink macules on the inner surface and simple trichomes in lower density; white exterior face, covered with simple trichomes, staminal tube 5 cm long, constricted to the median portion; stamens 5, distally free among each other, longitudinal fillaments 4.3 cm long, anthers 0.6-0.7 cm long, rimose, bitheca, glabrous, stigma 5-lobed; super ovary, with oil glands between the locules. Capsule 11-15 × 7 cm, oblong, 5-valvate, glabrous, valves 0.9-1.0 diam, epicarp porous, abundant wool. Seeds 0.7-0.6 mm long, reniforms.

Specimens examined: BRAZIL. PARAÍBA: Areia, Mata do Pau Ferro, 7º18’.07”S and 36º42’.24”W, 05.X.1999, fl., M.R. Barbosa 1843 (JPB); CCA, 6º58’.34”S and 35º41’.56”W 11.IX.2013, fl., L.P. Felipe 14.367 (EAN); Aroeiras, 7º35’.05”S and 35º42’.56”W, 27.IX.1994, fl., M.F. Agra et al. 3297 (JPB); Boa Vista, APA do Cariri, 7º18’.07”S and 36º42’.24”W, 28.VII.2016, fl., S.S. Figueiredo 22 (HACAM); 26.X.2016, fr., S.S. Figueiredo 35 (HACAM); Ibidem, São Joãozinho, 07º17’015”S and 036º16’567”W,17.VIII.2016, fl., S.S. Figueiredo 25 (HACAM); Cabaceiras, Lajedo de Pai Mateus, 7º27’.10”S and 36º19’.00”W, 22.IX.2007, fl., B.I. Lima; R.J. Lima; C.E.L. Lourenço; C.M. Pessoa & G.A. Costa 43 (JPB); Cajá, 7º12’.27”S and 35º20’.17”W, 14.X.1979, fl., M.F. Agra 180 (JPB); Campina Grande, 7º14’.34”S and 35º54’.05”W, 21.IV.1953, fl., L. Xavier s.n. (JPB 1714); Desterro, 7º18’.31”S and 37º05’.40”W, 10.XII.1993, Fl., M.F. Agra; E.A. Rocha; E. Locatelli; S. Formiga 2284 (JPB); Dona Inês, Mata do Seró, 6º36’.38”S and 35º38’.44”W 09.IV.2008, fl., K.R.F. Xavier 43 (EAN); Esperança, 7º01’.17”S and 35º51’.27”W, 07.XII.2015, fl., S.S. Figueiredo 09 (HACAM); Juarez Távora, 7º01’.24”S and 35º49’.16”W, 05.IX.1996, M.R. Barbosa 1530 (JPB); Lagoa Seca, Faz. Ipuarana, 7º08’.52’S and 35º51’.30”W, 25.IX.2001, fl., A. Serafim; G. Clara; E. Lourenço (JPB 28.660); Maturéia, Pico do Jabre, 7º17’.20”S and 37º23’.03”W, 27.IX.1997, fl., M.F. Agra; S. Cabral; R. A. Pontes; G. Baracho & E.A. Rocha 4358 (JPB); Patos, 7º02’.20”S and 37º26’.43”W, 10.VII.2012, fr., D.S. Lucena; C. D. Ferreira; P. C. Souto.(6018 CRST); Patos, 7º02’.20”S and 37º26’.43”W, 21.IX. 2011, M. Meneses (CSRT 002854); Pedra Lavrada, Serra da Flecha, 6º23’.50”S and 36º23’.50”W, 30.IV.2007, est., B.I. Lima; P.C. Gadelha-Neto; R.J. Lima & S.A. Melo (JPB 37012); Pico do Jabre, 7º17’.20”S and 37º23’.03”W, 23.IX.2003, M.M. Medeiros 40 (JPB); Pocinhos, 7º03’.20”S and 36º05’.29”W, 31.X.2007, fl., P.C. Gadelha-Neto & B.I. Lima s.n. (JPB 38.069); Ibidem, Bela Vista, 36º14’.15”W, 04.IX.2016, fl., S.S. Figueiredo 31 (HACAM); Ibidem, Sítio Bravo, 7º03’20”S and 36º05’29”W, 19.X.2015, fl., S.S. Figueiredo 06 (HACAM); 15.XII.2016, fl., S.S. Figueiredo 10 (HACAM); 24.I.2016, fr., S.S. Figueiredo 13 (HACAM); Puxinanã, Sítio Espinheiro, 7º08’.57”S and 35º50’.02”W, 27.VIII.2016, S.S. Figueiredo 27 (HACAM); 29.X.2016, fr., S.S. Figueiredo 36 (HACAM); Ibidem, Várzea Salgada, 7º08’57”S and 35º50’02”W, 16.X.2015, fl., S.S. Figueiredo 05 (HACAM); 16.VIII.2016, fl., S.S. Figueiredo 24 (HACAM); 12.IX.2016, fr., S.S. Figueiredo 33 (HACAM); São João do Cariri, Pai Mateus, 7º23’36.82”S and 36º18’09.96”W, 22.XII.1997, fl., C. Schlindwein 838 (JPB); Seridó, 6º54’.55”S and 36º27’.00”W, 13-IX-2005, fl., M.F. Agra; V.P.M. Coelho & I.J.L. Diniz 6529 (JPB); Serra Branca, Cacimba Nova, 7º33’18”S and 36º40’56”W, 28.VIII.2016. fl., S.S. Figueiredo 28 (HACAM); Serra da Raiz, Sítio Boa Ventura, 6º42’.14”S and 35º27’.25”W, 07.I.2012, fl., J.N.P. Cordeiro 43 (EAN); Solânea, 6º44’.26”S and 35º43’.24”W, 02.VIII.2001, fl., T.M. Grisi Velôso 271 (IPA); Teixeira, 7º13’14.85”S and 37º15’08.37”W, 15.IX.1984, fl., W.N. Fonseca 429 (RB).

Ceiba glaziovii (Figure 3 and 4) is a Brazilian endemic species from the northeastern region, in the states of Bahia, Ceará, Paraíba, Pernambuco, Rio Grande do Norte and Sergipe (Flora do Brasil 2020 in preparationFLORA DO BRASIL 2020 (in preparation). Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br (last access on 26/05/2019).
http://floradobrasil.jbrj.gov.br...
). The species can be easily recognized especially for presenting aculeate stems with, a protuberance in the middle region, five stamens, and by the white petals with lilac to pink macule sparsely arranged on the inner surface. This species had already been registered in the Caatinga vegetation of the study area; however, during the execution of this work, it was also recorded under the Atlantic Forest domain, which represents a new occurrence for this environment (Figure 5). In the study area, it was found flowering in January and from May to December, and fruiting in November.

Figure 3
Ceiba glaziovii. a. individual in flowering; b. individual fruit; c. flower and flower bud; d. stem tube; e. leaf; f. anthers; g. fruit; h. ovary; i. ovary demonstrating the nectariferous glands; j. fruit open; k-l. seeds.

Figure 4
Ceiba glaziovii. a. habit; b. inflorescence; c. flower; d. fruiting; e. fruit (Photos: a, b, e. Figueiredo, S.S.; c-d. Monteiro, F. K. S.).

Figure 5
Distribution of Ceiba glaziovii in the State of Paraíba, Brazil (Map: Rodrigues, E.M.).

2. Eriotheca Schott & Endl., Melet. Bot.: 35. 1832.

Eriotheca comprises 25 species restricted to South America (Duarte 2015DUARTE, M.C. 2015. Ceiba. In Lista de Espécies da Flora do Brasil. Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br/jabot/floradobrasil/FB9034 (last access in 26/05/2019).
http://floradobrasil.jbrj.gov.br/jabot/f...
). In Brazil, the species occur from the North to the South, associated with the Caatinga, the Cerrado, the Amazonian, and the Atlantic Forest, in deciduous, Seasonal and Ombrophiles forests, and in igapós (Flora of Brasil 2020 in preparation). It is characterized by stems without aculeous, leaflets with entire margin and slightly revolute, inflorescences with 1-10 cimes, receptacle with or without nectaries, indumentum lepidote, peltiform scales, starred trichomes, fruits capsules, obovoid, abundant wool, and numerous glabrous seeds (Duarte 2010DUARTE, M.C. 2010. Análise filogenética de Eriotheca Schott & Endl. e gêneros afins (Bombacoideae, Malvaceae) e estudo taxonômico de Eriotheca no Brasil. Tese de Doutorado, Instituto de Botânica da Secretaria de Estado do Meio Ambiente, São Paulo., Carvalho-Sobrinho 2013CARVALHO-SOBRINHO, J.G. 2013. A new species of Eriotheca (Malvaceae: Bombacoideae) from Espírito Santo, Eastern Brazil. Phytotaxa 108:49-53.). Two species were found in Paraíba: E. gracilipes and E. macrophylla, both associated with the Atlantic Forest vegetation.

2.1. Eriotheca gracilipes (K. Schum.) A. Robyns, Bull. Jard. Bot. l’état 33 (1/2): 145. 1963.

Trees, 3-17 m high; rectilinear stem, streaks absent, glabrescent. Stipules absent. Compound digitate leaves, 5-foliolate, pedicel ca. 1-3 cm long, leaflets 6-18 × 2-5 cm, lepidote, coriaceous, obovate, truncated apex, cuneate base, entire margin, slightly revolute, main vein protruding at the abaxial face, craspedodromous venation, secondary veins 10-15, evident, printed on abaxial face, glabrescent; petiole 3-27 cm long, with brown scales. Obovoid flower buds, axillary flowers, 1-5 in each cyme, 12-13 cm long, peltate brown scales, sparse, receptacle with nectaries forming a continuous ring, calyx 0.6-1.0 cm long, cupuliform, truncated, 5-slightly apiculate, externally lepidote-brown, internally not seen; corolla 1-1.8 cm long, narrow-obovate, acuminate apex, curved, both sides covered with starred trichomes, golden; petals cream to yellowish; staminal tube 3-5 cm long, constricted at the median portion until the base, stamens 110-160, longitudinal fillaments 3 cm long, anthers 0.05-0.1 cm long, reniform; ovary conic to subglobose, with peltate scales, 5-locules, pluriovulate; stylus 1-1.5 cm long. Capsule 4.0-7.0 × 2.0 cm, obovoid, dehiscent, 4-5 valves, acuminate to apiculate, base rounded, valves 0.5-1 cm long, glabrescents, coppery wool. Seeds not seen.

Specimens examined: BRAZIL. PARAÍBA: Cruz do Espírito Santo, Engenho São Paulo, 7º06’37.14” S and 35º05’42.93” W, 22.XI.1968, A. Lima 68-5491 (IPA).

Additional specimens examined: BRAZIL. DISTRITO FEDERAL: 15º48’45.12”S and 47º58’42.86”W, 25.IX.1989, fr., D. Alvarenga 466 (RB). GOIÁS, Pirenópolis,15º51’05.15”S and 48º57’30.83” W, 01.VIII.1984, fl., B.A.S. Pereira et al. 1102 (CEPEC); São Domingos, 16º34’40.85”S and 49º20’01.33”W, 13.VIII.1995, fl., B.A.S. Pereira & D. Alvarenga 2840 (RB).

Eriotheca gracilipes (Figure 6) occurs in Bolivia and Brazil (Tropics 2018). In Brazil, it is recorded in the North (Rondônia), Northeast (Bahia, Paraiba and Pernambuco), Midwest (Distrito Federal, Goiás, Mato Grosso do Sul, Mato Grosso) and Southeastern (Minas Gerais, São Paulo) regions (Flora do Brasil 2020 in preparationFLORA DO BRASIL 2020 (in preparation). Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br (last access on 26/05/2019).
http://floradobrasil.jbrj.gov.br...
). This species represents a new record for Paraiba and inhabits the Atlantic Forest vegetation (Figure 7). Additional material from the state of Pernambuco was also found during the morphological analyses. Eriotheca gracilipes is mainly characterized by the lcoriaceous leaflets, obovoid flower buds, and by the externally lepidote calyx. In the study area, it was found flowering in August and November, and fruiting in November.

Figure 6
Eriotheca gracilipes. a. habit; b. branches; c. inflorescence; d. flower; e. stamens (Images: a. Nascimento, W.P.; b, c, d. Beneli, A.; e. Penati, R.).

Figure 7
Distribution of the Eriotheca species found in the State of Paraíba, Brazil (Map: Rodrigues, E.M.).

2.2. Eriotheca macrophylla (K. Schum.) A. Robyns, Bull. Jard. Bot.l’état 33 (1/2): 152. 1963.

Trees, 10-20 m high; rectilinear stem, streaks absent, glabrescent, stipules absent. Compound leaves, digitate, 5-leaflet; petiole 2-15 mm long, leaflets 7.5-18 × 3.3-6.0 cm, lepidote, carthaceous, large-obovate to oblong, rounded apex, emarginate, decurrent base, entire margin, slightly revolute, with abundant peltate trichomes on the abaxial face, and peltate trichomes scarce on adaxial face, craspedodromous venation, main vein salient on abaxial face, secondary veins evident, printed on abaxial face. Oblong flowers buds, flowers axillary, 2-7 in each cyme, 2.5-3.0 cm long, pedicel 1-3.0 cm long, glabrescents, receptacle with or without nectaries, calyx 0.5-0.9 cm long, cupuliform, crenate margin, externally with flocculent trichomes, ferrugineous, internally not seen, petals 2.0-3.0 cm long, bright yellow, concave, obovate, rounded apex, recurved in the apical portion unilaterally, both sides covered with golden starred trichomes; staminal tube 0.4-0.5 cm long, constricted in the median portion to the base, 100-120 stamens, longitudinal fillaments 0.8-1.8 cm long, anthers 0.05 cm long, reniform; ovary globose to subglobose, flocculent coppery scales, 5 carpels, 5 locules, pluriovulate, stylus 1.3 cm long with flocculent coppery trichomes in the basal portion. Capsule 4.0-6.0 × 0.5-1 cm, obovoid, 5 valvate, acuminate, cuneate base, valves 2.0-3.0 cm long, glabrescent, abundant wool, brownish seeds not seen.

Specimens examined: BRAZIL. PARAÍBA: Areia, Mata do Pau Ferro, 6º58’.15”S and 35º44’.58”W 12.VII.2001, E. Cunha 30144 (JPB); João Pessoa, 7º07’13.31”S and 34º50’42.67”W, 23.XI.1979, M.F. Agra 200 (JPB); Ibidem, 7º07’13.31”S and 34º50’42.67”W,18.V.1993, fr., P. C. Gadelha-Neto 27 (JPB); Mamanguape, 6º50’22.95”S and 35º08’0814”W, 22.XI.1991, L.P. Félix & C.A.B. Miranda 4592 (EAN); Ibidem, Estação Ecológica do Pau Brasil, 6º36’15.30”S and 35º07’45.36”W, 06.I.2008, fr., S. Satyro & M.S. Pereira 40542 (JPB).

Additional specimens examined: BRAZIL. PERNAMBUCO: São Lourenço da Mata, Estação Ecológica do Tapacurá, 8º02’27.54”S and 35º11’46.51”W, 17.VIII.2001, K. Almeida 184 (JPB).

Eriotheca macrophylla is endemic from Brazil, occurring in the Northeast (Alagoas, Bahia, Pernambuco and Paraíba) and Southeast (Espírito Santo, Minas Gerais and Rio de Janeiro) regions, associated with the Atlantic Forest domain (Flora do Brasil 2020 in preparationFLORA DO BRASIL 2020 (in preparation). Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br (last access on 26/05/2019).
http://floradobrasil.jbrj.gov.br...
). This species is a new record for the State of Paraíba (Figure 7) can be easily recognized by the carthaceous leaflets; oblong flower buds, and the externally flocculent ferrugineous trichomes on the calyx. In the study area, it was found with flowers in June and with fruits in May, July and August.

3. Pseudobombax Dugand, Caldasia 2(6): 65. 1943.

This genus has 23 species, restricted to the Neotropical region (Duarte 2015DUARTE, M.C. 2015. Ceiba. In Lista de Espécies da Flora do Brasil. Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br/jabot/floradobrasil/FB9034 (last access in 26/05/2019).
http://floradobrasil.jbrj.gov.br/jabot/f...
). In Brazil, the species can be found in all the regions, inhabiting Ombrophylous forests, Semideciduous forests, Restinga, Caatinga, Cerrado, rocky field and ciliary forest, including in rocky outcrops (Flora do Brasil 2020 in preparationFLORA DO BRASIL 2020 (in preparation). Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br (last access on 26/05/2019).
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).

It is morphologically characterized by presenting the stem with green longitudinal streaks, which are spread throughout the plant, compound leaves and unifoliolate, polystemone flowers, bithecae, fruit a 5-valvate capsul, abundant wool and numerous seeds, reniform (Carvalho-Sobrinho & Queiroz 2010CARVALHO-SOBRINHO, J.G. & QUEIROZ, L. P. 2010. Three new species of Pseudobombax (Malvaceae, Bombacoideae) from Brazil. Novon 20:13-20.). In Paraíba, it is represented by three species: Pseudobombax marginatum, P. parvifolium and P. simplicifolium, associated with the Caatinga vegetation (Agreste and Sertão).

3.1. Pseudobombax marginatum (A.St.-Hil., Juss. & Cambess.) A. Robyns, Bull. Jard. Bot. l’État 33(1): 73. 1963.

Trees, 5-8 m high; large canopy. Irregular stem with amorphous excrescences, glabrescent, with yellowish-green longitudinal streaks. Stipules absent. Compound leaves, digitate, petiole 7.0-11.0 mm long, 5-7 foliolate, grouped at the apex of the branches, without braquiblasts; leaflets 6.5-14.5 × 4.0-8.1 cm, oblong-elliptical to elliptical, carthaceous, acuminate to obtuse apex, base cuneate and slightly attenuate, entire margin, adaxial face glabrous, face abaxial pubescent with branched trichomes under the vein, main vein salient on the abaxial face, secondary veins prominent, printed on the abaxial and adaxial face, craspedodromous venation. Terminal or subterminal flowers, solitary, 11-17.3 cm long, oblong to oboval buds, pedicel 2.0-3.0 × 0.4 cm, glabrous, glands in the pedicel connection with the calyx 2.3 × 2.5 cm, cupuliform to campanulate, truncated, inconspicuously 5-apiculate, externally with simple microtrichomes, internally glabrous; petals 12-14.8 × 1.5-2.0 cm, linear-lanceolate, acute apex, brown externally and sometimes with simple trichomes, internally white, pubescents, covered with simple trichomes; staminal tube 2.0 × 0.8 cm, glabrous, stamens fused only at the base of the tube and then free among each other; stamens 300-350, longitudinal fillaments free 10-11 × 3.5-4.0 cm, anthers 0.3-0.4 cm long, bithecae; ovary 5 mm long, oblong, subglabrous except for peltate microtrichromes, 5-locules, pluriovulate; stylus 14.5 mm long, glabrous. Capsule 13-15 × 4.0-6.0 cm, oblongoid, 5-valvate, apiculate apex, cuneiform base, valves 0.8-1.3 cm diam, glabrous, abundant gold wool. Seeds 0.5-0.6 cm long, piriform, light brown when immature and blackened when herborized.

Specimens examined: BRAZIL. PARAÍBA: Boqueirão, 7º28’36.94”S and 36º07’56.28”W, 22.VI.2011, I.V.P. Nóbrega 253 (CSTR); Campina Grande, INSA, 7º14’.34”S and 35º54’.05”W, 24.I.2011, A.S. Barbosa 1972 (EAN); Ibidem, INSA, 7º14’.34”S and 35º54’.05”W, 13.III.2012, fl., A.L.S. Albuquerque & D.S. Ferraz (EAN 19.617); Congo, 7º28’.33”S and 36º39’.01”W, 01.IX.2011, fl., s.c. (EAN 17.562); C.E.L. Lourenço; M.C. Pessoa & G.A. Costa 836 (JPB); Diamante, Fazenda Andresa, 7º25’21.33”S and 38º15’44.41”W, 02.V.2011, C.E.F. Diniz 2080 (CSTR); João Pessoa, Fazenda Santana, Sítio João do Cariri, 7º28’.33”S and 36º28’.55”W, 21.V.1997, R.G. Luna 01 (JPB); Patos, 7º01’.28”S and 37º16’.48”W, 21.VI.2014, fl., H.O. Machado-Filho 460 (IPA); Itaporanga, Fazenda Cafula e Lagoa, 7º18’13.28”S and 38º09’00.64”W, 21.IX.2014, P.F. Souza 43 (CSTR); Patos, Santa Terezinha, 7º02’.20”S and 37º26’.43”W,25.III.1993, fl., M.F. Agra; E.A. Rocha; E. Locatelli et al. & A.B. Fragoso 1729 (IPA); Pocinhos, Sítio Icó, 07º17’.015”S and 036º16’.567”W, 16.IX.2007, fl., L.E.T. Mendonça 34 (JPB); Ibidem, 7º4’28.39”S and 36º03’18.65”W, 21.VI. 211, I.V.P. Nóbrega, (2705 CSTR); Poço Dantas, Olho D’Água do Frade, 6º24’14.78”S and 38º29’47.98”W, 12.X.2007, I.B. Lima & P.C. Gadelha-Neto; J.R. Lima; C.E.L. Lourenço; M.C. Pessoa & G.A. Costa 836 (JPB); Riacho dos cavalos, 6º26’08.51”S and 37º39’07.08’W, 04.II.2014, fl., R.H. Silva (5959 CSTR); Santa Teresinha, 7º02’.20”S and 37º26’43”W, 24.VII.2013, A.E.S. Ferreira (4720 CSTR); Ibidem, 18.IV.2006, C.M.A. Pegado & L.P. Félix 08 (EAN); São João do Cariri, Estação Experimental, 7º28’.33”S and 36º28’.55”W, 25.VIII.1993, fl., C.M.L. Aguiar 35 (JPB); Ibidem, Riacho Aveloz, 7º28’.33”S and 36º28’.55”W, 18.VIII.2004, fl., A.V. Lacerda & F.M. Barbosa 225 (JPB); Ibidem, Riacho Gangorra, 7º28’.33”S and 36º28’.55”W 20.XII.2004, A.V. Lacerda & F.M. Barbosa 286 (JPB); Ibidem, Riacho Salgado, 29.IX.2004, A.V. Lacerda & F.M. Barbosa 222 (JPB); Ibidem, 22.VII.2005, A.V. Lacerda & F.M. Barbosa 495 (JPB); Ibidem, Riacho Aveloz, 7º28’.33”S and 36º28’.55”W 26.IX.2005, fl., A.V. Lacerda & F.M. Barbosa 509 (JPB); São José do Bonfim, Sitio Pé de Serra, 7º08’.43”S and 37º18’.59”W, 13.VII.2001, fl., M.G.V. Marinho 17 (JPB); São Mamede, 6º55’.26”S and 37º05’.02”W, 10.IX.2011, fl., s.c. (EAN 20.484); São José de Piranhas,7º07’08.10”S and 38º29’57.70”W, 5.VII.2011, P.F. Souza 26 (CSTR); Serra Branca, Serra do Jatobá, 7º33’.18”S and 36º42’.56”W, 29.VI.016, S.S. Figueiredo 17 (HACAM); Ibidem, 21.VII.2016, fl., S.S. Figueiredo 19 (HACAM); Ibidem, 04.VIII.2016. fl., S.S. Figueiredo 23 (HACAM); 09.IX.2016, fr., S.S. Figueiredo 32 (HACAM); Sousa, Fazenda Jangada, 6º45’.09”S and 38º13’.27”W, 2.III.1995, fl., P.C. Gadelha-Neto 205 (JPB); Ibidem, Vale dos Dinossauros, 6º45’.09”S and 38º13’.27”W, 06.VIII.2004, P.C. Gadelha-Neto 1220 (JPB); Sumé, Sítio Gonçalo, 7º39’.44’S and 36º54’.21”W, 12.VI.1999, F. Barbosa 24 (JPB).

Pseudobombax marginatum (Figure 8 and 9 h-n) occurs in Peru, Bolivia and Brazil, specifically in the North, Northeast, Midwest, Southeast, and South regions, under the domain of the Caatinga, Cerrado and Atlantic Forest, including the Seasonal Deciduos Forest (Flora of Brasil 2020 in preparation). The species is easily recognized by the irregular stem with amorphous excrescences and yellowish-green longitudinal streaks. In the study area (Figure 10), it was found flowering in March, June, and from August to November and fruiting in November.

Figure 8
Pseudobombax marginatum. a. stem; b. leaf; c. flower buds; d. inflorescence; e. flower; f. fruit (photos: Monteiro, F.K.S.; F. Rodrigues, E.M.).

Figure 9
Pseudobombax parvifolium. a. flower; b. stem; c. streaks; d. leaf; e. ovary; f. flower bud; g. fruit. P. marginatum. h. flower; i. leaf; j. flower bud; k. ovary; l. stem; m. streaks; n. fruit.

Figure 10
Distribution of the species of Pseudobombax found in the State of Paraíba, Brasil (Map: Rodrigues, E.M.).

3.2. Pseudobombax parvifolium Carv. -Sobr. & L.P. Queiroz, Novon 20(1): 17-19. 2010.

Trees, 8-12 m high; rectilinear stem, with dark green longitudinal streaks, glabrescent. Stipules absent. Compound leaves, digitate, pedicel 1.0 cm long, 5-7 foliolate, grouped at the apex of the branches, without braquiblasts; leaflets 8.0 cm × 0.3 cm, oval-lanceolate, carthaceous, elliptical, acuminate apex, cuneate base and slightly attenuated, revolute margin, irregularly crenulate, main vein salient on the abaxial face, 9-12 secondary veins, evident, printed on the abaxial face, glabrescent; craspedodromous venation; petiole 11 cm long. oblong-lanceolate buds. Terminal flowers, solitary, 10-17 cm long, curved; calyx 2.0 mm long, cupuliform to campanulate, truncated, sometimes inconspicuously 5-apiculate, externally puberulous with short trichomes, thick, internally sericeous on distal half; petals 12-15 cm long, white internally, linear-lanceolate, apex acute to acuminate, externally brown, usually in longitudinal strips when herborized, tomentose at the base, internally pubescent; staminal tube 8.8-9 cm long, stamens 400-450, fused only at the base of the tube and then free among each other; longitudinal fillaments free 8.5 cm long, anthers 0.3 cm long, bithecae; ovary 0.5-0.6 cm long, ovoid, subglabrous except for peltate microtricomes, 5-locules, pluriovulate; style 13.5 cm long, subglabrous except for peltate microtrichome in the basal portion. Capsule 10-14 × 5 cm, oblong to oblong-elliptic, 5-valves, apiculate, cuneiform base, valve 1 cm diam, glabrous, woody, light-brown to cream wool. Seeds 0.9 cm long, reniform, light to dark-brown.

Specimens examined: BRAZIL. PARAÍBA: Boa Vista, APA do Cariri, 7º18’.07”S and 36º42’.24”W, 26.X.2016, fl., fr., S.S. Figueiredo 34 (HACAM); Pocinhos, Bela Vista, 7º03’.20”S and 36º05’.29”W, 04.IX.2016, fl., S.S. Figueiredo 30 (HACAM); Ibidem, Bravo, 7º03’.20”S and 36º05’.29”W, 16.XI.2015, fl., S.S. Figueiredo 07 (HACAM); Ibidem, 15.XII.2015, fr., S.S. Figueiredo 11 (HACAM); 24.I.2016, S.S. Figueiredo 15 (HACAM); Ibidem, 10.VII.2016, S.S. Figueiredo 18 (HACAM); Soledade, 07º03’26’S and 36º21’.46”W, 04.VII.2006, R.F.P. Lucena & G.R. Almeida 246 (PEUFR).

Pseudobombax parvifolium (Figure 9a-g and 11)is endemic from Northeastern Brazil, in the states of Bahia and Sergipe, inhabiting Caatinga environments (Flora do Brasil 2020 in preparationFLORA DO BRASIL 2020 (in preparation). Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br (last access on 26/05/2019).
http://floradobrasil.jbrj.gov.br...
). It can be easily recognized by the rectilinear stem with dark-green longitudinal streaks and the reniform seeds. In the study area (Figure 10), it was found flowering from September to December, and fruiting in October and December.

Figure 11
Pseudobombax parvifolium. a. habitat; b. stem; c. flower bud; d. flower; e. fruit (Photos: Figueiredo, S.S.).

3.3. Pseudobombax simplicifolium A. Robyns, Bull. Jard. Bot. l’État 33: 81. 1963.

Trees, 6-12 m high; stem with irregular green rectilinear streaks. Triangular stipules, concave. 3-foliolate, united at the apex in braquiblasts, leaves and branches with peltate and dense microtrichome among each other; pedicel 16 mm long, leaflets 6-7 × 1.0-1.1 cm, oval-elliptic to oval-lanceolate, coriaceous, carthaceous, acute apex, base obtuse, margin revolute, glabrous on both sides, main vein salient, secondary and tertiary veins evident; craspedodromous venation; petiole 1.5 cm long. Oblong flower buds, terminal flowers, solitary or in groups with 2-3, 10-11 cm long, sometimes striated longitudinally, glabrous; calyx 2.2 × 1.1 cm, campanulate, usually 5-apiculate, externally subglabrous due to sparse and peltate microtrichomes and internally, sericeous; petals 8-9 × 0.7-0.8 cm, brown when dry (not seen in nature), lanceolate, acute apex, with simple microtrichomes, internally sericeous; staminal tube 1.1 cm long, 200-300, stamens fused only at the base of the tube and then free among each other, glabrous; fillaments free 60-100 mm long, anthers 0.2-0.4 cm long; ovary 0.6 × 0.2 cm, oblong, glabrous, 5-locules, pluriovulate; style 7-12 cm long. Capsule 1.2 × 0.7 cm, oblong to obovoid, valves not observed, abundant light brown wool. Seeds 0.4-0.5 cm long, piriform, dark brown.

Specimens examined: BRAZIL. PARAÍBA: Aroeiras, 7º35’.05”S and 35º42’.24”W, 24.IX.1994, fl., M.F. Agra et al. 3298 (JPB).

Additional specimens examined: BRAZIL. BAHIA: Luiú, 14°24’45.96’’S and 43°33’16.58’’W, 16.VII.2005, fl., R.C. Forzza, B.R. Silva & R. Dias-Melo 4065 (RB). BAHIA: Curaçá, Faz. Angical, 9º15’40.48”S and 39º43’38.44”W, s.d., fr., S.B. Silva 303 (CEPEC).

Pseudobombax simplicifolium (Figure 12) is endemic from Brazil, occurring in the Northeast (Bahia, Pernambuco, Piauí, Sergipe) and Southeast (Minas Gerais) regions, associated with the Caatinga domain (Flora do Brasil 2020 in preparationFLORA DO BRASIL 2020 (in preparation). Jardim Botânico do Rio de Janeiro. http://floradobrasil.jbrj.gov.br (last access on 26/05/2019).
http://floradobrasil.jbrj.gov.br...
). In this work, it is reported as a new occurrence for Paraíba and inhabits the Caatinga vegetation (Figure 10). Morphologically, P. simplicifolium is characterized by presenting 3-leaflets leaves united at the apex in braquiblasts. In the study area, it was found flowering in November.

Figure 12
Pseudobombax simplicifolium. a. branches; b. leaf; c. flower bud; d. flower; e. fruit; f. kapok (photos: b-e. Carvalho-Sobrinho; a, f. Siqueira-Filho, J.A.).

  • Ethics
    This study doesn’t involve dealing with humans.
  • Data availability
    The data recorded in this work will be available in GenBank.

Acknowledgements

To the CNPq (National Scientific and Technological Development Council), by Scientific Initiation Scholarship granted to S.S. Figueiredo. The State University of Paraíba (UEPB), support for the development of this work. J.I.M. Melo thanks to the CNPq (National Scientific and Technological Development Council), for the Research Productivity Scholarship (PQ-2 Proc. n. 303867/2015-9). Regina Alcântara, by producing the illustrations in Nanjing. Erimágna de Moraes Rodrigues, for the production of the map.

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Publication Dates

  • Publication in this collection
    18 May 2020
  • Date of issue
    2020

History

  • Received
    20 July 2019
  • Reviewed
    13 Mar 2020
  • Accepted
    18 Mar 2020
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