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Redalyc.Leaf Dimorphism of Microgramma Squamulosa

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Redalyc.Leaf Dimorphism of Microgramma Squamulosa Revista de Biología Tropical ISSN: 0034-7744 [email protected] Universidad de Costa Rica Costa Rica Dalgallo Rocha, Ledyane; Droste, Annette; Gehlen, Günther; Lizandro Schmitt, Jairo Leaf dimorphism of Microgramma squamulosa (Polypodiaceae): a qualitative and quantitative analysis focusing on adaptations to epiphytism Revista de Biología Tropical, vol. 61, núm. 1, marzo, 2013, pp. 291-299 Universidad de Costa Rica San Pedro de Montes de Oca, Costa Rica Available in: http://www.redalyc.org/articulo.oa?id=44925650016 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Leaf dimorphism of Microgramma squamulosa (Polypodiaceae): a qualitative and quantitative analysis focusing on adaptations to epiphytism Ledyane Dalgallo Rocha1, Annette Droste1, Günther Gehlen1 & Jairo Lizandro Schmitt1 1. Programa de Pós-Graduação em Qualidade Ambiental, Universidade Feevale, RS 239, 2755 - Novo Hamburgo-RS, 93352-000, Brazil; [email protected], [email protected], [email protected], [email protected] Received 08-XII-2011. Corrected 04-VIII-2012. Accepted 03-IX-2012. Abstract: The epiphytic fern Microgramma squamulosa occurs in the Neotropics and shows dimorphic sterile and fertile leaves. The present study aimed to describe and compare qualitatively and quantitatively macroscopic and microscopic structural characteristics of the dimorphic leaves of M. squamulosa, to point more precisely those characteristics which may contribute to epiphytic adaptations. In June 2009, six isolated host trees cov- ered by M. squamulosa were selected close to the edge of a semi-deciduous seasonal forest fragment in the municipality of Novo Hamburgo, State of Rio Grande do Sul, Brazil. Macroscopic and microscopic analyzes were performed from 192 samples for each leaf type, and permanent and semi-permanent slides were prepared. Sections were observed under light microscopy using image capture software to produce illustrations and scales, as well as to perform quantitative analyses. Fertile and sterile leaves had no qualitative structural differences, being hypostomatous and presenting uniseriate epidermis, homogeneous chlorenchyma, amphicribal vascular bundle, and hypodermis. The presence of hypodermal tissue and the occurrence of stomata at the abaxial face are typical characteristics of xeromorphic leaves. Sterile leaves showed significantly larger areas (14.80cm2), higher sclerophylly index (0.13g/cm2) and higher stomatal density (27.75stomata/mm2) than fertile leaves. The higher sclerophylly index and the higher stomatal density observed in sterile leaves are features that make these leaves more xeromorphic, enhancing their efficiency to deal with limited water availability in the epiphytic environ- ment, compared to fertile leaves. Rev. Biol. Trop. 61 (1): 291-299. Epub 2013 March 01. Key words: fertile leaf, sterile leaf, fern, epiphyte, morphometry, xeromorphism. Epiphytes are important components of many different environments. Hietz & Briones the biodiversity of tropical forests, although (1997) studied the adaptations to epiphytism little is known about their structural charac- of Pleopeltis mexicana (Fée) Mickel & Bei- teristics. Ferns form a group of plants that tel. (Polypodiaceae), Phlebodium areolatum should receive special attention in the epiphytic (Humb. & Bonpl. ex Willd.) J. Sm. (Polypo- environment, considering that about 2 600 spe- diaceae) and Elaphoglossum glaucum T. Moore cies around the world are epiphytic (Kress (Dryopteridaceae), and found an association 1986). Because of microclimate variations in between water availability and stomatal den- epiphytic environments, these plants develop sity. Ribeiro et al. (2007) analyzed the leaf adaptations (Benzing 1990), which are phy- anatomy of Anemia tomentosa (Savigny) Sw. siological and structural changes that reduce var. anthriscifolia (Schrad.) Mickel and Ane- water loss (Jones 1987, Hietz & Briones 1997), mia villosa Humb. & Bonpl. ex Willd. (Ane- and mechanisms that help them to capture light miaceae), linking it with adaptative strategies (Graçano et al. 2001). to hydric stress on rocky outcrop. The purpo- Studies about leaf anatomy are an impor- se of most comparative anatomic studies of tant tool to identify differences between plant ferns is to describe terrestrial species and to organs and adaptive strategies developed in contribute to their taxonomic classification, Rev. Biol. Trop. (Int. J. Trop. Biol. ISSN-0034-7744) Vol. 61 (1): 291-299, March 2013 291 as in the studies conducted by Hernández et Epiphytic species of Polypodiaceae deve- al. (2006) with species of Dryopteris Adans. loped various adaptive strategies to deal with (Dryopteridaceae) and by Hernández et al. a limited availability of water which include a (2008) with species of Cheilanthes Sw. (Pte- wide variation of anatomical and morphologi- ridaceae). Tejero-Díez et al. (2010) compa- cal characters (Dubuisson et al. 2009). The aim red anatomically the Polypodium plesiosorum of this study was i) to describe and compare sensu Moran (Polypodiaceae) group, in order qualitatively and quantitatively macroscopic to identify taxonomic characteristics. However, and microscopic structural characteristics of most studies have been focused on epiphytic the dimorphic leaves of M. squamulosa, and angiosperms (Zanenga-Godoy & Costa 2003, ii) to point more precisely those characteristics Proença & Sajo 2007, Noguera-Savelli & Jáu- which contribute to adaptations in the epiphytic regui 2011). environment. Polypodiaceae shows pantropical distribu- tion, with about 12 000 species (Smith et al. MATERIAL AND METHODS 2008). Microgramma C. Presl sensu Tryon & Tryon (1982) comprises of 30 species (Sali- Study area: Fertile and sterile leaves of no et al. 2008). Their leaves are glabrous or M. squamulosa were collected in the munici- scaly, monomorphic or dimorphic (Tryon & pality of Novo Hamburgo, State of Rio Grande Tryon 1982) with a coriaceous texture, which do Sul (RS), Brazil, in an area close to the edge is an adaptation to the epiphytic environment of a fragment (29º46’51.4’’ S-50º58’31.6’’ W) (Hirsch & Kaplan 1974). Microgramma squa- of the semi-deciduous seasonal forest (Teixeira mulosa Kaulf. de la Sota is an epiphytic fern et al. 1986) located in an Area of Special Envi- occurring in Peru, Bolivia, Brazil, Argenti- ronmental Interest. The predominant regional na, Paraguay and Uruguay (Tryon & Stolze climate, according to Köeppen, is classified as 1993), both in human-modified environments Cfa type, being humid-temperate, with rainfall (Gonçalves & Waechter 2003) and in natural throughout the year (Moreno 1961). forests (Kersten & Silva 2002). This species presents a long rhizome from which arise the Sampling: In June 2009, six isolated host petioles of the fertile and sterile leaves, which trees (phorophytes) covered by an extensive M. are dimorphic (Sehnem 1970, Jaime et al. squamulosa rhizome (Fig. 1A) were selected 2007, Suffredini et al. 2008). Hirsch & Kaplan (1974) studied the orga- nography and development of the shoot sys- tems of M. squamulosa and M. vacciniifolia (Langsd. & Fisch.) Copel. to establish their taxonomic differences. The antiulcer action of M. squamulosa has been studied by Suffredini et al. (1999). Jaime et al. (2007) described the diagnostic characteristics of M. squamulosa to contribute to its taxonomic identification and to the control of the quality of secon- dary metabolites with medicinal properties. Stem and root morphology and anatomy of M. squamulosa have been characterized in the pharmacognostic study conducted by Suffre- dini et al. (2008). However, these studies did not analyze the structural differences between Fig. 1. (A) Microgramma squamulosa habit; (B) fertile dimorphic leaves. leaf; (C) sterile leaf. Bar: 2cm. 292 Rev. Biol. Trop. (Int. J. Trop. Biol. ISSN-0034-7744) Vol. 61 (1): 291-299, March 2013 next of the edge of the forest fragment. For by Feder & O’Brien (1968), and according to each leaf type (Fig. 1B, 1C), 192 samples the manufacturer’s instructions. The samples were collected, 32 from each phorophyte. The were embedded transversally. Samples were leaves were collected from the internal area of sectioned at a thickness of 7µm using a rotatory the phorophyte canopy, where they received microtome (Leica RM 2125 RT) with dispos- sunlight from the East and were exposed to a able blades (Leica 818). The sections were luminosity range of 22.99 to 38.73µmol/m2/s. stained with 0.05% toluidine blue (Sakai 1973) Voucher material was deposited in the Herba- and mounted using synthetic resin (Entellan®). rium Anchieta of the Universidade do Vale do The semi-permanent slides of paradermal sec- Rio dos Sinos (PACA 108023), in São Leopol- tions were obtained after dissociation (Franklin do, RS, Brazil. 1946) of other 36 leaves of each type, which were later stained with 0.05% toluidine blue Macroscopic and microscopic analyses: (Sakai 1973), mounted on 50% glycerin and For macroscopic analyses, 120 leaves of each luted with clear nail polish (Purvis et al. 1964). type were used. They were scanned and their Slides were mounted with epidermis samples images were digitalized using a desktop scan- of the two faces of the leaves to classify the ner connected to a computer. The leaves were leaves according to the occurrence of stomata. dehydrated in an oven at
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