Nectar is an aqueous solution produced by specialized structures (nectaries), largely distributed among angiosperms (Fahn 1979; Smets 1986; Nepi et al. 2009). The ontogenetic origin, size, shape or position of floral nectaries is variable among eudicotyledonous flowers (Pacini et al. 2003; Evert 2006; Bernardello 2007), and show no particular patterns associated with taxa, habitat or pollinator type (Herrera et al. 2006; Canto et al. 2007; Agostini et al. 2011; Wilmer 2011). Despite being referred to as a poorly elaborated carbohydrate-based solutions, nectar production requires extensive processing by the nectary cells, whose subcellular features reflect its final composition (Nepi 2007).
Nectar has been considered the most important resource available to anthophilous animals in angiosperms (Galetto & Bernardello 2005; Willmer 2011). Bignoniaceae species are predominantly zoophilous (Gentry 1974; Alcantara & Lohmann 2010) and the floral nectar production has been commonly attributed to a conspicuous nectary, characterized as a disk that surrounds the ovary base (Gentry 1992; Galetto 1995; 2009; Rivera 2000). This nectariferous disk is usually composed by a secretory epidermis and secretory parenchyma, predominantly supplied by phloem (Galetto 1995; Thomas & Dave 1992; Rivera 2000; Guimarães et al. 2016). However, in some genera as Clytostoma, Cydista, Phryganocydia (now treated as Bignonia according to Lohmann & Taylor 2014) and Lundia the nectariferous disk is absent, and these nectarless flowers are supposed to be pollinated by deceit (Gentry 1980). Remarkably, Lundia cordata, a Bignoniaceae species that possesses a vestigial and non-secretory disk, offers nectar as trophic resource, which production was assigned to the corolla-borne trichomes (Lopes et al. 2002). A similar pattern was described for Zeyheria montana, for which a functional disk is supposedly lacking (Gentry 1992) and floral nectar secretion was also attributed to the corolla-borne trichomes placed on the nectar chamber's inner corolla wall (Bittencourt & Semir 2004). So, for species in which the disk is absent or reduced, as L. cordata and Z. montana, the trichomes' carpet was considered as a substitute nectary (sensuVogel 1997) considering that this type has evolved secondarily, after the disk lost its secretory function (Lopes et al. 2002; Bittencourt & Semir 2004). Despite the importance of this evolutionary change in the floral nectary in Bignoniaceae, these functional assumptions have been based only on disk size and on the distribution, abundance and histochemistry of corolla-borne trichomes in the nectar chamber. However, ultrastructural and chemical analyses are essential to investigate relationships between structure and cell functions (Fakan 2004).
Zeyheria genus is characterized as possessing a vestigial, non-functional nectary disk (Gentry 1992). This genus comprises only two species and both differ on their pollinators. Zeyheria montana is hummingbird-pollinated and produces copious diluted nectar (Bittencourt & Semir 2004), while Z. tuberculosa is bee-pollinated and produces a more concentrated nectar in smaller amounts (Souza 2015). Carrying-out a study on gynoecium secretory trichomes of Zeyheria montana (Machado et al. 1995; 2006) authors observed abundant starch grains in the reduced disk and presence of vascular tissues close to the disk. These observations led us to question the non-functionality of the reduced disk, since such attributes have been associated with nectar production (Fahn 1979; Nepi 2007). Additionally to the already described involvement of corolla-borne glandular trichomes in nectar secretion (Bittencourt & Semir 2004), we observed signs of secretory activity in other tissues and structures of the nectar chamber, which suggest that, in this species, floral nectary may comprise more than one site of secretion.
These observations motivated us to investigate, in a comparative way, the chemical and subcellular features of the reduced disk, aiming to determine its functionality, in both Zeyheria species since they differ in nectar volume and concentration. In addition, we investigated all the nectar chamber's tissues and structures in order to determine the functional role of each one and to characterize the floral nectary in both species.
Materials and methods
Plant species, sampling and study site
Zeyheria montana Mart. and Z. tuberculosa (Vell.) Bureau ex Verl. differ in relation to habit, type of vegetation, pollinators and nectar attributes (Gentry 1992; Rizzini 1997). Zeyheria montana is a typical shrubby species, hummingbird-pollinated with diluted and copious nectar, that occurs in the Brazilian savanna (Bittencourt & Semir 2004). Zeyheria tuberculosa is a tree species, bee-pollinated with little and more concentrated nectar that occurs in seasonal semi deciduous forests in Brazil (Souza 2015).
This study was conducted from 2008 to 2015 on five adult specimens of Z. montana and five of Z. tuberculosa growing in savanna and forest areas, respectively, at Botucatu municipality, São Paulo State, Brazil (22°55'S 48°30'W). Anthesis in Z. montana lasted about six days and around four days in Z. tuberculosa and in both species nectar production started in pre-anthesis buds. From each individual four pre-anthesis buds and four first-day functional flowers (n = 20 samples per species), both stages showing nectar production, were collected. The flowers were observed and dissected under a stereomicroscope. Then, 20 samples of each stage were fixed for anatomical (five samples) and histochemical (five samples) studies on light microscopy (LM) and for ultrastructural studies on scanning (SEM) (five samples) and transmission (TEM) (five samples) electron microscopy.
Voucher of Z. montana (number 28469-28470) and of Z. tuberculosa (number 30818-30819) are deposited on BOTU Herbarium.
Scanning electron microscopy (SEM)
For SEM, the samples (n = 10 plants) were fixed in 2.5% glutaraldehyde (GA) in 0.1 M phosphate buffer (pH 7.2), dehydrated in an ethanol series, dried by the critical point method using liquid CO2, and sputter-coated with approximately 10 nm of gold (Robards 1978). The materials were observed in a FEI Quanta 200 SEM (FEI, Hillsboro, OR, USA) at 20 kV.
Light microscopy (LM)
For LM, the samples were fixed in FAA 50 (formaldehyde, acetic acid, and 50% ethanol 1:1:18 v/v) (Johansen 1940), dehydrated in an ethanol series, and embedded in methylmethacrylate-based resin. Semi-thin sections (5-6 µm) were cut with disposable steel razors on a RM2255 (Leica) rotary microtome, mounted on glass slides and stained with 0.05% Toluidine Blue O (pH 4.3) (O'Brien et al. 1964). Fresh hand-cut sections and semi-thin sections were treated with Sudan III (Johansen 1940) for total lipids; Lugol's reagent for starch grains (Johansen 1940); NADI reagent for terpenes (David & Carde 1964); Dragendorff reagent for alkaloids (Svendsen & Verpoorte 1983); mercuric bromophenol blue to detect total proteins (Mazia et al. 1953); Fehling's solution to detect reducing sugars (Purvis et al. 1964). Samples treated with aluminium trichloride and lead neutral acetate (Charrière-Ladreix 1976) were analysed under fluorescence microscope for flavonoids. Standard control procedures were carried out simultaneously. Starch grains and calcium oxalate crystals were detected using polarized light. The preparations were examined and photographed using an Olympus BX-51 microscope (Olympus, Tokyo, Japan) with Image-ProExpress software (Media Cybernetics Inc., Silver Spring, Maryland, USA).
Transmission electron microscopy (TEM)
For conventional ultrastructural analysis, samples of pre-anthesis buds and first-day functional flowers were fixed in glutaraldehyde (2.5% with 0.1 M phosphate buffer, pH 7.3, for 6-8 h at 4 °C), post-fixed with 1% osmium tetroxide (OsO4) aqueous solution in the same buffer, for 2h at room temperature. Samples were then dehydrated using a graded acetone series and embedded in Araldite resin at room temperature. Polymerization was performed at 60 °C for 48 h. Ultra-thin sections were stained with uranyl acetate and lead citrate (Reynolds 1963), and examined with a TEM Tecnai Spirit (FEI) at 60 kv. In addition, samples were treated with ZIO method (zinc iodide-osmium tetroxide) to improve the visualization of endomembranes (Reinecke & Walther 1978).
The micromorphology, histochemistry, anatomy and ultrastructure of the reduced disk and of all the other tissues and structures that comprise the nectar chamber were characterized in this study. The similar results are presented for the two studied Zeyheria species and the differences between them were highlighted in the text. Additionally, due to anatomical, histochemical and ultrastructural similarities, the data from disk and stipe were grouped and presented together. As no differences were found in any of the secretory tissues and structures between pre-anthesis and first-day functional flowers, the results were presented only for functional flowers.
Nectar chamber micromorphology
Both Zeyheria species had similar nectar chamber morphology (Fig. 1), showing four regions with secretory features: the reduced disk (Fig. 2), the stipe (Fig. 3), the petals' axils (Fig. 4) and the floral tube internal wall (Figs. 5, 6).
The tubular flowers of both Zeyheria species accumulated nectar, since pre-anthesis stage, in a chamber located at the base of the floral tube, which was delimited by an upper constriction formed by the thickened bases of epipetalous filets disposed around the ovary (Fig. 1A).
The reduced nectary disk, in both species of Zeyheria, was flattened, protuberant, and occurred at the base of the stipe (Fig. 1A-C), but in Z. montana it was more conspicuous (Fig. 1B). The disk's surface was sparsely covered with trichomes in both species (Fig. 1B-C), while the stipe was densely covered by glandular and non-glandular trichomes (Fig. 1A-C). In both species, prominent modified stomata were distributed throughout the disk's surface and remnants of the flocculent secretion could be observed especially around the stomata (Fig. 1D). The inner surface of the nectar chamber was lined with glandular capitate-type trichomes (Fig. 1A, E-H) distributed among papillae (Fig. 1F-G), except on the corolla tube's base, which was glabrous (Fig. 1E). The papillae exhibited variable sizes and verrucose cuticle (Fig. 1F-G). Cuticle blisters resulting from subcuticular secretion accumulation in the distal region of the capitate trichomes' head cells (Fig. 1H) were registered since the pre-anthesis stage.
The histochemical tests revealed the presence of flavonoids, starch grains, reduced sugars, terpenes/ resin and total lipids in both species (Tab. 1). Disk-stipe and petal's axil reacted positively for starch grains, reduced sugars, and total lipids. Only capitate trichomes' head cells reacted positively to terpenes/ resin and total lipids tests. Papillae reacted positively to total flavonoids and lipids. Proteins were detected only in Z. montana, which occurred in the disk-stipe and papillae.
|Reagents||Target compounds||Colour||Disk and stipe||Petals' axil||Capitate trichomes||Papillae|
|Z. m.||Z. t.||Z. m.||Z. t.||Z. m.||Z. t.||Z. m.||Z. t.|
|Lead neutral acetate||Flavonoids||Yellowish||-||-||-||-||-||-||+||+|
|Mercuric bromophenol blue||Proteins||Blue||+||-||-||-||-||-||+||-|
|Sudan III||Total lipids||Orange-red||+||+||+||+||+||+||+||+|
- negative, + positive
Nectar chamber histology and ultrastructure
The reduced disk (Fig. 2) and the stipe (Fig. 3) were composed by a uniseriate epidermis and covered by a thin cuticle, a nectary parenchyma formed by isodiametric and compactly arranged voluminous cells, and a subnectary parenchyma constituted by larger loosely arranged cells and vascularized mainly by phloem, showing well-developed intercellular spaces (Fig. 2A). Xylem was abundant in the junction of the disk's base to the petals' axils (Fig. 2A).
By TEM, both epidermal and parenchyma cells of the disk (Fig. 2B) and stipe (Fig. 3A) presented similar features. In both Zeyheria species these cells had conspicuous nuclei with evident nucleolus, abundant cytoplasm and vacuoles of variable sizes (Figs. 2B, 3A). Big starch grains occurred in all the disk and stipe cells showing a clear decrease in abundance and size from the parenchyma towards the epidermis (Figs. 2B, 3A-C). Epidermal and parenchyma cells exhibited dense cytoplasm with abundant ribosomes (Figs. 2C, 3B), mitochondria (Figs. 2D, 3B), endoplasmic reticulum (Figs. 2F-H, 3B, G), Golgi bodies (Figs. 2D, G, I, 3B-D) and round plastids (Figs. 2B-C, 3A-C), which contained big starch grains and lipid droplets in both species, and protein bodies in Z. montana (Fig. 2C). Plastids with residual starch grains occurred in subepidermal parenchyma cells (Fig. 3E). Endoplasmic reticulum (Fig. 2G-H) and Golgi bodies and associated vesicles (Figs. 2G, I, 3C-D) were better viewed with the use of the ZIO method. In addition, parenchyma and epidermal cells showed juxtaposed vesicles with plasma membrane (Figs. 2F, 3G), cytoplasmic oil bodies (Figs. 2E, H, K, 3C, E, G), and multivesicular bodies (Fig. 2F, J). Protein bodies were abundant in Z. montana disk and stipe cells, occurring inside plastids (Fig. 2C) and scattered in the cytoplasm (Fig. 2C, J), while these inclusions were absent in Z. tuberculosa. The vacuoles contain finely flocculent material (probably the polysaccharides previously detected with histochemical tests) and electron-lucent material (oils), besides membranous material (Figs. 2E, J, K, 3E, G). Sieve tube elements of large calibre with companion and parenchyma cells were registered in the parenchyma of the disk and stipe (Fig. 2L; 3F). Wall protuberances coated with the plasma membrane were observed on the entire inner wall surface of the stipe parenchyma cells (Fig. 3B). The anticlinal walls of epidermal cells showed primary pit fields with abundant plasmodesmata (Fig. 2E, M). Accumulations of dense material traversing the inner and outer periclinal walls, in the cytoplasm and vacuoles besides lipid drops on the cuticle surface were commonly observed in epidermal cells (Fig. 2M). Developed periplasmic space containing dense or flocculent material was observed in the epidermal (Fig. 2F, M) and parenchyma cells (Figs. 2G, 3E, G). Intercellular spaces, variable in extension and width, filled with finely flocculated material (polysaccharides), were observed in the parenchyma tissue (Figs. 2N, 3G).
The petals' axils (Fig. 4) exhibited uniseriate epidermis composed by small cells irregular in shape, covered by a smooth and thin cuticle, and subepidermal parenchyma composed by compactly arranged small cells of various shapes (Fig. 4A). Ultrastructurally, epidermis and parenchyma cells were characterized by presenting thickened walls, conspicuous nuclei, dense cytoplasm and vacuoles of different sizes (Fig. 4B). Amyloplasts filled with conspicuous starch grains (Fig. 4B-C), endoplasmic reticulum (Fig. 4D-F), hyperactive well-developed Golgi bodies (Fig. 4C-D) and mitochondria (Fig. 4C) were the most evident organelles in these cells. Conspicuous oil bodies occurred scattered in the cytoplasm (Fig. 4D, F). The vacuoles presented flocculent material and membrane debris (Fig. 4C). Images of vesicle juxtaposed to the plasma membrane (Fig. 4D), which was sinuous in outline (Fig. 4D-F), were frequently observed in these cells. Flocculent material occurred in the periplasmic space of those cells (Fig. 4D-F). Just in the petal junction to the disk, the thickness of epidermal cells' walls was remarkable (Fig. 4E). The swelling of the middle lamellae and its posterior dissolution along the anticlinal walls of the epidermal cells originated channels that exhibited accumulated secretion (Fig. 4E).
The glandular capitate trichomes (Fig. 5) were composed by an epidermal basal cell, a uniseriate stalk formed by 1-5 cells, and a secretory head with 12-24 cells concentrically disposed in one or two layers. Trichomes, with a variable number of cells in the stalk and secretory head, occurred side-by-side (Fig. 1F-H). The glandular trichomes were covered with a thick cuticle that was thicker on the lateral walls of the stalk cells (Fig. 5A-B). Cuticle blisters, originated by the secretion accumulation between the cell walls and cuticle, were more evident in the distal pole of the secretory head (Figs. 1H, 5B, G). Prior to the accumulation of secretion in the subcuticular space, the outer periclinal walls of the head cells showed a homogenous polysaccharide inner stratum that was followed by a dense intermediate fibrous layer, which protruded towards the cuticle layer forming a network of electron-dense ramifications in this cuticle region (Fig. 5C). The dissolution of the intermediate polysaccharide layer preceded the cuticle detachment from the outer cell wall (Fig. 5F). The cells from the secretory head showed a central and spherical nucleus, vacuoles of variable sizes and shapes, and dense, abundant cytoplasm (Fig. 5A-B). Polyribosome (Fig. 5C, E-F), globular mitochondria with a well-developed cristae (Fig. 5F, G), scarce Golgi bodies (Fig. 5E), extensive profiles of rough endoplasmic reticulum (Fig. 5F) and dilated smooth endoplasmic reticulum (Fig. 5C, G), and modified plastids (Fig. 5G-I) characterized the cytoplasm of the head cells. The plastids were large, round (Fig. 5H) or oval (Fig. 5I) and filled with tubular electron-dense structures and osmiophilic inclusions of different sizes. In the head cells, it was remarkable the abundance of scattered electron-lucent droplets (Fig. 5D) and electron-dense inclusions (Fig. 5D-H), previously identified as lipids. Some head cells exhibited a developed periplasmic space with irregular contour and accumulations of heterogeneous materials (Fig. 5F-G, I). These cells had sinuous walls with a loose aspect (Fig. 5F). Subcuticular space occurred through all the extension of the head cells (Fig. 5B, F), although it was more developed in the apical pole of the secretory head (Fig. 5B, G). The subcuticular space contained abundant lipid accumulations and some flocculated material (Fig. 5G).
Papillae (Fig. 6) were covered with a thick and folding cuticle forming tall, deep sulci at the cell surface (Fig. 6A). These cells exhibited sinuous thin walls interconnected by abundant plasmodesmata (Fig. 6A). Cytoplasm was abundant (Fig. 6A) and rich in polyribosomes, globular mitochondria, plastids (Fig. 6B-D), Golgi bodies, rough endoplasmic reticulum and multivesicular bodies (Fig. 6C). Mitochondria showed well-developed cristae and black granulations (Fig. 6C). Plastids lacking inner membrane and exhibiting inclusions of different aspects, including deeply electron-dense bodies (flavonoids), electron-lucent drops (oils) and granular material (proteins) were registered (Fig. 6B-D). Figures suggesting the fusion of rough endoplasmic reticulum profiles with the plasma membrane were commonly registered (Fig. 6C). Osmiophilic bodies, previously identified as flavonoids, occurred inside plastids (Fig. 6B-D), attached to the inner tonoplast surface (Fig. 6D) and scattered through the cytoplasm (Fig. 6A, D). Conspicuous protein bodies occurred inside plastids (Fig. 6C-D) and scattered through the cytoplasm (Fig. 6D).
Our data support that the reduced disk, stipe, petals' axils, glandular trichomes and papillae have subcellular evidences of secretory activity. In both species, disk, stipe and petals' axils are involved in hydrophilic secretion, while capitate glandular trichomes in lipophilic secretion and papillae in mixed secretion. We present strong evidence that although reduced in size, the nectary disk is functional in nectar secretion in both Zeyheria species. It is important to emphasize that the disk-stipe differ in the cellular contents. In Z. montana proteins are predominant, while in Z. tuberculosa lipids droplets are more abundant. Lipids and proteins, or their derivatives, as amino acids, have been described as nutritionally valuable nectar componentes that contribute to its attractiveness for various mutualistic animals (Baker & Baker 1983; González-Teuber & Heil 2009).
Our study clearly showed that the disk, in spite of the reduced dimensions, has a functional vascularized parenchyma that storages and hydrolyses starch, besides presenting typical cellular features associated to nectar-producing tissues, including large mitochondria, rough endoplasmic reticulum (RER), well-developed Golgi bodies and abundant vesicles (Fahn 1979; 1988; Roshchina & Roshchina 1993; Nepi 2007). These evidences show that the disk in the Zeyheria genus is functional in nectar secretion. This finding differ from Bittencourt & Semir (2004) that referred the disk in flowers of Z. montana as vestigial, non-functional and ascribing nectar secretion to the corolla-borne glandular trichomes.
As both, disk and stipe, were similar in ultrastructure and histochemistry we considered them as a functional unity involved in nectar secretion, herein called 'disk-stipe'. We hypothesized that nectar production in the stipe may compensate for the disk's reduced size, since there is a considerable increase in area of tissues with secretory activity. In fact, a considerable amount of nectar is produced from the pre-anthesis buds, mainly in Z. montana (Machado et al. 2006). Nectar release may occur through modified stomata placed only at the disk, similar to what is reported for other Bignoniaceae species (Guimarães et al. 2016) and through the intact cuticle, as reported by Nepi (2007) for several other plant species, since we didn't find cuticle pores. The dense trichomes coverage in the stipe did not allow us to verify the occurrence of modified stomata in this region. The presence of amyloplasts with voluminous starch grains was remarkable in the disk-stipe parenchyma cells of both Zeyheria species. These starch grains showed a gradual reduction in size and in abundance from the parenchyma cells toward the epidermis. Other authors, like Nepi (2007 and references therein) have described a similar pattern in different species and believe that starch grains' hydrolysis in the nectary parenchyma contributes directly to nectar carbohydrate's supply, which reinforces our findings about the disk-stipe functionality. We detected an abundance of proteins in the cellular contents of Z. montana. In fact, proteins and amino acids were detected in the floral nectar of this plant species (E. Guimarães unpubl. res.). The presence of proteins in nectar has been registered since the 1930's and several functions have been ascribed to them (Beutler 1935; Pryce-Jones 1944; Baker & Baker 1975). The proteins and amino acids registered in the floral nectar of several plant species may represent a nitrogen source for nectarivorous pollinators (Nicolson & Thornburg 2007), as the hummingbirds that feed on the nectar of Z. montana flowers.
The disk-stipe was supplied predominantly by phloem, and, probably, the pre-nectar flows away from the sieve tubes through an apoplastic route via intercellular spaces reaching the modified stomata (e.g. Wist & Davis 2006). In fact, we observed intercellular spaces filled with flocculent material in the nectary parenchyma tissue of both species. Furthermore, a symplastic pathway of pre-nectar can also occur in the floral nectary via the plasmodesmata, which connects phloem and nectary cells (Wist & Davis 2006; Vassilyev 2010). Additionally, stipe's parenchyma cells presented a peculiar feature, e.g. the presence of protuberances along the inner surface of the cell wall, which characterizes them as transfer cells. These protuberances are surrounded by plasma membrane and greatly enlarge the protoplast's surface, favouring transport by apoplast and symplast (Taiz & Zeiger 2013). Transfer cells were reported for several hydrophilic glands such as salt glands and nectaries (Fahn 1979). Moreover, the considerable plastid-juxtaposed mitochondria population observed in these cells is evidence of a secretion mechanism that requires enhanced energy, which is typical of transfer cells (Razem & Davis 1999).
The presence of oil droplets in plastids, inside vacuoles and dispersed in the cytoplasm of the nectary cells of all tissues and structures suggest that it may participate in the enrichment of floral nectar with lipids (Gilbert & Raven 1975), similar to reported for other Bignoniaceae species (Baker & Baker 1975; Guimarães et al. 2016).
The petals axil's cells have a similar subcellular pattern observed in the disk-stipe in both studied species. The presence of amyloplasts with signs of starch grains degradation, rough endoplasmic reticulum and hyperactive Golgi bodies in the petals axil's cells is typical of nectar secreting cells (Fahn 1979; 1988). RER and polyribosomes are evidence of enzymes synthesis that may act in the middle lamellae dissolution (Turner & Croteau 2004), besides contributing to the enrichment of floral nectar. In addition, the epidermal cells' variation in size and shape originates an irregular surface and amplifies the area of nectar release in this region of the nectar chamber. So, the petals' axils seem to have an important role in nectar release, in addition to the modified stomata.
The present study suggests that glandular capitate trichomes are involved in lipophilic secretion, instead of nectar secretion, as previously reported by Bittencourt & Semir (2004). The extensive development of plastids containing tubular osmiophilic structures and electron-dense droplets, together with the proliferation of smooth endoplasmic reticulum, have been described in many lipophilic secretory structures, particularly in those secreting terpenes (Cheniclet & Carde 1985; Figueiredo & Pais 1994; Ascensão et al. 1997; Monteiro et al. 1999; Turner et al. 1999; Machado et al. 2006; Possobom et al. 2015; Sá-Haiad et al. 2015). Terpenes were histochemicaly detected in capitate glandular trichomes in both Zeyheria species, which may participate in the attraction of mutualists or in the deterrence of antagonists (Harborne 1997; Nishida 2002; Raguso 2004; Machado et al. 2006; Guimarães et al. 2008).
The presence of polyribosomes, Golgi bodies and rough endoplasmic reticulum elements in these cells can be related to the increased cytoplasmic enzyme synthesis needed for cell metabolism and terpene biosynthesis (Turner & Croteau 2004). Furthermore, such organelles are also associated to the synthesis of the pectinases and cellulases involved in the wall degradation processes during the subcuticular space development (Ascensão et al. 1997; Machado et al. 2006). In fact, in both studied species, we observed sinuous, loose walls together with cuticle detachment in the head secretory cells.
Some papillae ultrastructural features from both Zeyheria species, such as abundant cytoplasm with modified plastids, abundance of RER, and presence of osmiophilic drops and protein bodies are consistent with secretion activity. We believe that the osmiophilic inclusions observed in the plastids, cytoplasm and vacuoles may be flavonoids, since these compounds were histochemically identified in the papillae. Flavonoids are a remarkably diverse group of polyphenolic secondary metabolites with a vast array of biological functions, such as defense against pathogenes, cell cycle inhibition, chemical messengers, control of auxin transport and stress protection (Roshchina & Roshchina 1993; Petrussa et al. 2013). Flavonoids are synthesized by a cytosolic multienzyme complex loosely associated to membranes of different organelles, such as the cytoplasmic face of the endoplasmic reticulum, vacuoles, plastids and nucleus (Petrussa et al. 2013). We hypothesize that the papillae contributes, in some way, for nectar secretion or nectar enrichment.
This study showed that all structures and tissues of the nectar chamber have secretory activity and we suggest that, in some way, all of them are involved in nectar secretion, characterizing a complex and integrated system of floral nectar production in Zeyheria species. This kind of nectary system is a novelty, since it comprises several tissues and structures functioning in an integrated fashion. Thus, in spite of its reduction in size, the disk is functional in nectar secretion in both Zeyheria species. This finding contradicts the previous general assumptions that reduced disks in Bignoniaceae are non-functional in nectar secretion. Therefore, the use of routine methods together with ultracytochemical techniques in transmission electron microscopy allowed us to investigate more accurately the relationship between cell structure and function. Our results highlight the importance of detailed cytological and cytochemical studies in order to assess the functionality of floral nectaries with different developmental degrees in Bignoniaceae. Therefore, other Bignoniaceae genera are under study to verify if our findings on Zeyheria genus can be extended to other species with reduced nectary disk.