Abstract:Colleters are common secretory structures in Rubiaceae. In this study, we describe colleter morphoanatomy and histochemistry in 10 species belonging to Chiococceae, Coussareae, and Psychotrieae tribes of Rubiaceae. Colleter morphoanatomy was analyzed by light and scanning electron microscopy. Microscopy analysis revealed that colleters were present on the stipule adaxial surface in all species. In the case of Palicourea marcgravii A.St.-Hil. and Chiococca alba Hitchc., colleters were also found on leaf primord… Show more
“…Morphologically distinct types of colleters have been reported in the literature (Lersten 2008;Thomas 1991;Silva et al 2017), and the distribution, typology and the presence of calcium oxalate crystals are characters frequently used in taxonomic (Lersten 1974;Coutinho et al 2015;Lopes-Mattos et al 2015) and evolutionary approaches (Vitarelli et al 2015;Judkevich et al 2017). The standard colleter type, formed by a non-secretory parenchyma axis covered by palisade secretory epidermis (Fahn 1988;Thomas 1991), is the most common and has been recorded in several unrelated families such as Euphorbiaceae (Machado et al 2015;Vitarelli et al 2015;Feio et al 2016), Rubiaceae (Lopes-Mattos et al 2015Judkevich et al 2017) and Salicaceae (Fernandes et al 2016;Faria et al 2019), but only for Macrocarpea obtusifolia in Gentianaceae (Dalvi et al 2014a).…”
“…Morphologically distinct types of colleters have been reported in the literature (Lersten 2008;Thomas 1991;Silva et al 2017), and the distribution, typology and the presence of calcium oxalate crystals are characters frequently used in taxonomic (Lersten 1974;Coutinho et al 2015;Lopes-Mattos et al 2015) and evolutionary approaches (Vitarelli et al 2015;Judkevich et al 2017). The standard colleter type, formed by a non-secretory parenchyma axis covered by palisade secretory epidermis (Fahn 1988;Thomas 1991), is the most common and has been recorded in several unrelated families such as Euphorbiaceae (Machado et al 2015;Vitarelli et al 2015;Feio et al 2016), Rubiaceae (Lopes-Mattos et al 2015Judkevich et al 2017) and Salicaceae (Fernandes et al 2016;Faria et al 2019), but only for Macrocarpea obtusifolia in Gentianaceae (Dalvi et al 2014a).…”
“…Colleters are widely distributed on young vegetative and reproductive organs in plants and have been reported in ferns (Oliveira et al 2017), monocots (Leitão & Cortelazzo 2008;Mayer et al 2011;Cardoso-Gustavson et al 2014) and in sixty-five eudicots families (Thomas 1991;Muravnik et al 2014) such as Apocynaceae, Gentianaceae, Rubiaceae, (Thomas 1991;Renobales et al 2001;APG 2009;Lopes-Mattos et al 2015;Tresmondi et al 2015). Anacardiaceae (Lacchia et al 2016), Aquifoliaceae (González & Tarragó 2009), Euphorbiaceae (Machado et al 2015;Vitarelli et al 2015), Fabaceae (Barros & Teixeira 2016), Lecythidaceae (Paiva 2012), Moraceae (Machado et al 2013), Rutaceae (Macêdo et al 2016), Rhizophoraceae (Sheue et al 2012) and Myrtaceae (Silva et al 2012).…”
Colleters are secretory structures that produce a sticky substance, consisting of a mixture of mucilage, proteins, terpenes, pectic substances and even alkaloids, which lubricates and protects the shoot apical meristem. Several colleter types have been described and have taxonomic value in many botanical families. In Myrtaceae, the colleters description is recent and presents three new morphological types (conic, euryform and petaloid) that differ those already described for other eudicots. In this work, we report the colleters morphological types in six species of three genera belonging to the Myrteae tribe of Myrtoideae from the Brazilian Cerrado. The samples were fixed for light and scanning electron microscopy. Histochemical tests were carried out on the fresh and methacrylate-embedded material. The conic and euryform colleters from Myrtoideae species of the Cerrado did not differ either morphologically nor as to the secretion nature from those described for Myrtoideae species from others biomes, which may indicate their potential use for taxonomic purposes. Considering the hypothesis that the multiple fleshy-fruit lineages have evolved independently in Myrteae tribe, our results indicate the relevance of additional studies in order to recognize the pattern of distribution of colleters in Myrtaceae.
“…Colleters produce a sticky secretion that functions as a lubricant, protecting meristems and developing organs against desiccation and attack by pathogens (Thomas, ; Mayer, Cardoso‐Gustavson & Appezzato‐Da‐Glória, ; Mayer, Carmello‐Guerreiro & Mazzafera, ). Colleters occur on the adaxial surface of young reproductive and (or) vegetative organs in several families of eudicots (Fahn, ; Thomas, ; Klein et al ., ; Martins, ; Coelho et al ., ; Dalvi et al ., ; Lopes‐Mattos et al ., ) and only Orchidaceae among monocots (Leitão & Cortelazzo, ; Mayer et al ., ). Recently, colleters have also been reported at the leaf margins for some species (Paiva, ; Mercadante‐Simões & Paiva, ; Vitarelli et al ., ; Feio, Riina & Meira, ).…”
Salicaceae possess a range of leaf teeth types, many characterized as nectariferous salicoid or violoid teeth. One large genus, Casearia, deviates from this generalization in having theoid teeth. Although taxonomic descriptions of Casearia have included reports of glands at the apex of teeth, there have been no descriptions of their anatomy or functional role. Here, we aim to describe the anatomy of the theoid teeth of 43 Casearia spp. Leaf samples from herbarium specimens were processed for light and scanning electron microscopy. Leaves of C. sylvestris were collected and fixed in the field for histochemical tests, revealing only polysaccharides in secretory epidermal cells and outside of these cells. The glands have precocious development and are composed of a non-vascular central axis covered with a palisade-like secretory epidermis. During senescence, the cells of the palisade-like secretory epidermis and central axis appear to lose their typical form, with some cell walls disintegrating. In the mature leaf, an abscission zone at the base of the gland causes detachment of the gland. The placement, anatomical structure, precocious activity and polysaccharide secretion (in C. sylvestris) allow the recognition of the glands associated with the marginal teeth in Casearia as colleters. Similar studies are needed for other genera in order to clarify how colleters have evolved in Salicaceae and how they are functionally and anatomically related to other teeth types in the family.
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