A structural review of foliar glands in Passiflora L. (Passifloraceae)

Extrafloral glands in Passifloraceae species have aroused the interest of many researchers because of their wide morphological diversity. The present work analyzed the foliar glands on 34 species of Passiflora from samples containing glands in the petiole and foliar blade fixed in 50% solution of formaldehyde-ethanol-acetic acid and stored in a 70% ethanol solution. For anatomical analyses, part of the material was embedded in Paraplast, longitudinally sectioned and double stained with safranin and astra blue. Scanning electron microscopy analysis was also carried out. To analyze the presence of sugars in the secretion of foliar glands, a glucose strip test was used. Based on the results of morphological, anatomical and glucose strip tests, the foliar secretory glands in Passiflora can be grouped into two categories: Type I glands, defined as nectaries, can be elevated or flattened, and can have a sugar content high enough to be detected by the glucose strip test analysis. Type II glands are elevated and did not show a positive reaction to the glucose strip test. From an anatomical viewpoint, glands characterized as extrafloral nectaries show a multistratified secretory epidermis, typically followed by two flat layers of nectariferous parenchyma with dense content. Internal to these layers, vascular bundles are immersed in the subsecretory parenchyma and terminate in phloem cells. On the other hand, type II glands show a single layer of elongated secretory epidermal cells. Internal to this single layer, parenchyma and vascular tissue with both phloem and xylem elements can be observed. The analyzed species show a wide diversity of gland shape and distribution, and the combined analysis of morphology, anatomy and preliminary tests for the presence of glucose in the exudate in different Passiflora subgenera suggests the occurrence of two categories of glands: nectaries and resin glands.


Introduction
Admired for the beautiful flowers and their edible fruits, the Passifloraceae Juss. Ex. Rouseel family is the object of study in different areas. Passiflora L. is the most representative genus in the Passifloraceae s.s. family, comprising more than 500 species [1][2][3][4]. According to the most recent infrageneric classification the family is subdivided in five subgenera, including PLOS  composition of the exudate. The authors verified that the exudate was soluble in ethanol and xylene, but not in water, and they also found osmiophilic material within the vacuole of secretory cells. According to the authors, Passiflora foetida shows a variability in its gland morphology and physiology that can be regarded as a transition from a true EFN to lipophilic secretory glands, thus naming them as resin glands. Detailed investigation to elucidate the morphological and anatomical structures of foliar glands in Passiflora has not been conducted. To better understand the diversity of secretory glands, the current study was aimed at comparative morphological and anatomical analyses associated with the presence of glucose in the exudate, as determined by the glucose strip test. We described two categories of secretory glands and discuss the use of terms regarding the different shapes.

Materials and methods
Thirty-four species were selected from the subgenera Astrophea (DC.) Mast. (1 species), Deidamioides (Harms) Killip (2 species), Decaloba (DC.) Rchb. (5 species) and Passiflora (26 species) ( Table 1), and special attention was given to the subgenera Passiflora, given its greater diversity. Part of the analyzed species was cultivated in a greenhouse at the Institute of Biosciences of the University of São Paulo. Another part was obtained from cultivation at Embrapa Cerrados (Brasilia, Federal District, Brazil), from a greenhouse cultivation at the State University of Santa Cruz (UESC, Ilhéus, Bahia, Brazil), and from the greenhouse of a private collector. One species was obtained from its natural environment (S1 Table). The voucher material was deposited at the Herbarium of the Botany Department at the University of São Paulo (SPF). Voucher numbers of private collectors were also used for obtaining information about where the species were originally sampled (S1 Table).
In order to structurally characterize the glands, samples were analyzed through scanning electron microscopy (SEM) and the shape definition was based on the descriptions for solid shapes by Radford et al. [22] and the terminology followed Harris & Harris [23]. Samples were fixed in a 50% solution of formaldehyde-ethanol-acetic acid (FAA 50) for 24 hours [24], dehydrated in ascending ethanol series, and then submitted to critical point drying with carbonic gas (CPD 030, Balzer). After drying, samples were mounted in metal stubs and metalized with gold [25]. The analysis was carried out using a QUANTA 250 (FEI COMPANY) scanning electron microscope at the Laboratory for Electron Microscopy of the Santa Cruz State University (UESC, Ilhéus-BA) and using a Zeiss DSM 940 scanning electron microscope (Zeiss, Oberkochen, Germany) at the Institute of Biosciences, University of São Paulo (IB/USP).
For the anatomical analysis, samples of petiolar and laminar glands were fixed in FAA 50 for 24 hours [24] and subsequently stored in a 70% ethanol solution. The material was dehydrated in a butanol series [26] and embedded in Paraplast (Leica Microsystems, Heidelberg, Germany). Longitudinal anatomical sections of the glands varying from 8 to 12 μm thick were cut in a Reihertt-Jung Auto Cut 2040 rotatory microtome and mounted on permanent slides. Material was double stained with a 1% safranin solution in 50% ethanol and a 1% astra blue solution, and mounted on permanent slides with Canada balsam [27]. Acquisition of photographic data was carried out by using a Leica DMLB microscope coupled to a Leica DFC 310FX camera and by using the IM50 software at the Plant Anatomy Laboratory (IB/USP).
In order to analyze the presence of sugars in the secretion of foliar glands, the glucose strip test was used (Inlab Diagnóstica-Alamar Tecno Científica Ltda.) for the species cultivated at the Institute of Biosciences, University of São Paulo. The same method was used for the species Passiflora sublanceolata (Killip) MacDougal cultivated in a Passiflora active germplasm bank at UESC (BAG-Passifloras).

Results
In the studied species of Passiflora, glands were found in the petioles (petiolar glands) in pairs or dispersed over the petiole at the margin of the leaf blade (marginal glands), on the abaxial face of the leaf blade and/or dispersed on both sides of the foliar blade (laminar glands). In the same species, glands could be seen in more than one region, and the most common combination observed was the presence of petiolar and marginal glands on the same leaf (Table 1). Based on the results of morphological, anatomical and glucose strip tests (Figs 1-3), the foliar secretory glands in Passiflora could be grouped into two categories: Type I glands, either elevated or flattened; and Type II glands, which are elevated (Table 1).
Type I Glands-These leaf glands have a sugar content high enough to be detected by the glucose strip test, and as such, they may be defined as nectaries (Fig 1). Nectaries are   anatomically formed by palisade secretory epidermis, which is usually multi-layered, followed by secretory parenchymal cells formed by juxtaposed cells with dense content and filled by subsecretory parenchyma cells with large cells in a loose arrangement. Two morphological patterns are described. Pattern I is characterized by well-structured glands with evident projection in relation to the foliar tissue. Pattern II is characterized by glands with tissue closely pressed against the leaf blade tissue, in which the projection is not very evident.
In pattern I, several forms can be grouped (Figs 2 and 3). In Passiflora deidamioides, the glands found in the petiolule are patelliform, i.e., sessile, rounded, and with a slight depression in the central region ( Fig 4A). On the other hand, the glands of the petiole are more elongated with an elliptic-patelliform shape, and a more evident depression in the central region ( Fig  4B). This elliptic-patelliform shape also occurs in petiolar and marginal glands of P. incarnata (Fig 4C and 4D. The petiolar glands of Passiflora coccinea, P. galbana, P. maliformis and P. setacea are spheroidal, with a flattened or slightly convex surface (Fig 4E-4H). The glands on the abaxial surface of leaf blade of P. coccinea and the marginal glands of P. gardneri, P. mierssi, P. sidifolia and P. subrotunda are lenticular ones (Fig 4I-4M). In some glands, a distension of the cuticle occurs, probably owing to the accumulation of exudate in the subcuticular space (Fig 4H and 4K).
In Passiflora sidifolia (Fig 4M), the marginal glands have different shapes. Some glands are more elongated than those previously described, and thus termed as elliptic-lenticular glands. This form also occurs in the marginal glands of P. eichleriana, P. haematostigma, P. umbilicata and P. serratodigitata (Figs 4N-4P and 5A). Besides having elliptic-lenticular glands in the leaf margins, P. serratodigitata ( Fig 5A) may also have semi-spheroid glands in this region. This shape is also found in the marginal glands of P. watsoniana (Fig 5B). These glands are sessile, circular, and widely convex.
A slightly different shape from those previously mentioned is the ellipsoid one. The ellipsoid shape occurs in the petiolar glands of P. ambigua, P. contracta, P. haematostigma, P. laurifolia, P. odontophylla and P. racemosa (Fig 5C-5H). These glands are sessile, more elongated in their longitudinal axis, have a convex central region, and their margins join gently to the petiole. In P. haematostigma and P. odontophylla (Fig 5E and 5G) non-glandular trichomes were observed in the nectariferous epidermis, most abundantly in P. haematostigma.
The petiolar glands of P. actinia, P. elegans, P. miersii and P. subrotunda (Fig 5I-5L), as well as the marginal glands of P. elegans and P. kermesina (Fig 5M and 5N, in frontal view), are sessile and display an obconical shape, being circular and slightly tapered towards the insertion in the petiole, with the apex flattened or slightly convex. In P. actinia, a curvature is seen towards the abaxial region of the petiole (Fig 5I).
Similarly to the previous form, we have identified obconical short-stipitate glands in which a short stipe ends in an obconical shape. These glands occur in the petiole of P. eichleriana and P. sidifolia, in which they make a curvature towards the abaxial region of the petiole, as well as in P. watsoniana (Fig 5O, 5P and 6A) and in the leaf margin of P. edmundoi (Fig 6B).
On the petiole of Passiflora edmundoi and P. kermesina, an obconical long-stipitate gland is observed with a stipe three times longer than that of short-stipitate glands (Fig 6C and 6D). A variation of this type of gland is noted in P. ligularis, in which a long stipe ends in a nearly obconical shape, but without inserting itself centrally in the stipe. This gland was determined to be obconical asymmetric long-stipitate ( Fig 6E).
In Passiflora morifolia (Fig 6F and 6G) and P. serratodigitata (Fig 6H), the petiolar glands show a very short stipe ending in a cotyliform shape. Here, the central region is deep, and the margins of glands form a cup shape.
The crateriform shape occurs in the short-stipitate petiolar glands, as observed in P. ferruginea and P. suberosa. These glands are circular and flat, with a shallow depression in the central region (Fig 6I and 6J).
Among the nectaries that follow pattern II, the glands on abaxial surface of leaf blade have the shape of a rounded spot, which may form a slight depression, termed as concave ocellus, or a slight bulging, termed as convex ocellus (Fig 2). In P. ferruginea, P. misera, and P. organesis, a pair of ocellus concave glands (Fig 6K and 6L) are usually observed in the region among the main vascular bundles at the base of the foliar blade, as well as convex ocellus glands (Fig 6M) dispersed in the foliar blade. In P. contracta, the glands on abaxial surface of leaf blade are convex ocellus only (Fig 6N). Slight concave ocellus glands also occur at the margin of the leaf blade in P. galbana and P. odontophylla (Fig 6O and 6P). These glands are minute and hardly recognizable to the naked eye.
The secretory epidermis is usually located in the central region of the glands. In some cases, it is restricted to either one of the sides, occupying a region that is proportionally small relative to the total size of the glandular projection (S1-S4 Figs). A subcuticular space is formed by distension of the cuticle caused by the accumulation of exudate (Fig 7A). Epidermal cells are generally elongated in the anticlinal direction, but they may vary from short to elongated (Fig  7 and Table 1). The nuclei are relatively large, usually centralized (Fig 7D), and the cell content is dense. The number of cells layers constituting the secretory epidermis can be variable in the same species and even in the same gland (Table 1). In P. racemosa, a predominant single layer of elongated cells is observed to form the secretory epidermis. However, regions with more Foliar glands in Passiflora L. than one layer are often found in the same nectary (Fig 7E). The non-secretory epidermis only shows one layer of cells with a slightly evident nucleus and a large vacuole.
Multicellular and unicellular non-glandular trichomes can be found in the secretory epidermis of P. coccinea and P. haematostigma (Fig 7G). Extensions of the subepidermal parenchyma occur in the regions underlying the base of the trichomes.
Internal to epidermis, the secretory parenchyma is usually formed by small cells, which can be flattened (Figs 7C, 7D, 7F and 7I and 8A), and have an evident nucleus and dense content. In P. haematostigma and P. laurifolia, the border between this region and the cells of the subsecretory parenchyma is unclear. In P. haematostigma the cells are slightly smaller and more juxtaposed than the innermost layers, and they are apparently derived from the hypodermis by periclinal divisions (Fig 8B). In P. laurifolia, the secretory parenchyma cells are smaller than those of subsecretory parenchyma and with a dense cytoplasma content (Fig 8C).
The innermost region of the glands is formed by non-secreting parenchyma (subsecretory), vascular bundles and idioblasts with druses (Figs 7 and 8). This is a highly variable region in that it can form glandular projections (S1- S4 Figs). Generally, the extension of the subsecretory parenchyma of marginal glands is limited to a few layers of cells. In this regard, the marginal gland of P. watsoniana is particularly short. Extension of the subsecretory parenchyma in petiolar glands is particularly notable in P. ligularis (S3D Fig). In glands on the abaxial surface of leaf blade, the subsecretory parenchyma replaces the palisade parenchyma present in the rest of the foliar blade, thus forming a very distinct region of parenchyma with rounded cells and large vacuoles occupying most of the cells (Fig 8F and 8G).
Vascularization of the glands occurs up to the region of the subsecretory parenchyma and consists of collateral bundles. In most species, the endings only consist of phloem cells (Fig 7C  and 7I), but in P. gardneri vascular endings are composed of both phloem and xylem cells ( Fig  8H).
In petiolar glands, the vascularization can show many ramifications (Fig 8I) or a single bundle such as that found in the marginal glands (Fig 7A). In the glands of abaxial surface of leaf blade, general vascularization runs parallel to the leaf surface, with the phloem tissue closer to the secretory tissue (Fig 8F and 8G).
Gland type II-A single pattern was observed for this glandular type, which did not show a positive reaction to the glucose strip test. These glands may be found in the petiole or across the entire foliar blade, showing a minute size, and thus being easily mistaken for trichomes (Fig 9). Anatomically, these glands have secretory epidermis with a single layer of anticlinally elongated cells. No distinction can be observed between secretory and non-secreting parenchyma (Fig 10).
In P. arida and P. villosa, the petiolar and laminar glands found on both sides and on the margin of the leaves are elongated, with trichomes along the stipe and with a rounded apex (Fig 9A and 9B). These are termed "terete" glands (Fig 3). On the other hand, the petiolar and laminar glands of Passiflora foetida, termed pyriform long-stipitate, do not show trichomes in their long stipes, but the termination is globose with an acuminate apex (Figs 3 and 9C). Similar to these glands are the non-marginal laminar glands of P. sublanceolata, which differ in the globular, non-pyriform termination observed in the previous description. They may be denominated as capitate long-stipitate (Figs 3 and 9E). Clavate glands at the margins of the leaf blade and in the petiole are found in Passiflora sublanceolata (Figs 3, 9E and 9F).
In these species, the glands are elongated with the secretory region restricted to the apex, and formed by palisade secretory epidermis (Fig 10A-10E). The epidermal cells of the stipe region are periclinally elongated, short in the anticlinal direction (Fig 10B), and in P. arida and P. villosa, trichomes are found along it. The inner region has few layers of parenchyma cells, some of which have druses (Fig 10C). The vascular system is central, and it has xylem and phloem endings. A gradual tapering in the secretory region of Passiflora foetida ends with the two most apical cells (Fig 10C). In Passiflora sublanceolata, the petiolar and marginal glands have a broader secretory region that extends almost to the middle part of the gland (Fig 10D). In addition, the subepidermal cells are wider in the petiolar glands of P. sublanceolata ( Fig  10D) which has fewer druses than what is found in P. foetida. In Passiflora arida, the secretory region is more restricted, with shorter secretory cells with thin walls (Fig 10A).
In Passiflora villosa, some secretory epidermal cells divide (Fig 10E). However, a multiseriate epidermis does not occur, as it does in species that have nectaries. In the subepidermal layers, lignified parenchyma occurs in some glands (Fig 10E). Foliar glands in Passiflora L.

Discussion
Our comparative study has revealed a variety of forms among the extrafloral secretory glands. Therefore, we were able to classify them into two distinct categories. Type I glands can be elevated or flattened, and have a sugar content high enough to be detected by the glucose strip test. These glands are defined as nectaries. Type II glands are elevated, but show no positive reaction to the glucose strip test. With few exceptions, nectar secreting glands are present in Passiflora [5,8], and the presence of EFN in Passifloraceae, as well as their shape, position and number, have been used as an important diagnostic feature for species or groups of species within the family [2][3][4][5][6][7][8][9][10].
Passiflora subgenera show EFN distributed as distinct features. Astrophea has two petiolar nectaries near the leaf blade; nectaries are absent on the leaf blade. Deidamioides has two petiolar nectaries or inconspicuous nectaries at the margin of the leaf blade; nectaries can also be absent on the leaf blade. Decaloba has two (rarely more than four) petiolar nectaries, when present, and leaf blades with nectaries in the shape of spots. Passiflora has two to six petiolar nectaries (rarely absent or more than six), and in the foliar blades nectaries may be either absent or present (marginal ones) [1,2]. Tetrapathea has petiolar nectaries, up to two per petiole when present, in ovoid, sub-sessile or crateriform shapes. When present, it has up to eight laminar nectaries that are ovoid and, in some cases, inserted in pairs between the median and primary veins at the base of the leaf blade, or even dispersed along the major veins [3].
Among the analyzed species, we found considerable morphological diversity in the glands of the subgenus Passiflora, many species displaying both petiolar and laminar glands in the same specimen. As mentioned in the description of the subgenus, the laminar glands observed in the present study were marginal, with the exception of the glands of the abaxial surface of leaf blade of P. coccinea. Still, Silva et al. [28] reported the occurrence of ocellus EFN on abaxial surface of leaf blade in at least one species of the subgenus Passiflora, P. glandulosa Cav. In the subgenus Decaloba, the analyzed species have only one type of gland, either petiolar or dorsolaminar, except for P. ferruginea, which has petiolar glands and ocellus glands on abaxial surface of leaf blade. Among the species belonging to the subgenus Deidamioides, P. deidamioides show features in common with those described for the group, with two petiolar nectaries, in this case, nectaries are also present in the petiolule. However, for P. contracta, besides the petiolar nectaries, nectaries in the abaxial surface of leaf blade are also present. Unlike the description for the group, P. haematostigma, from the subgenus Astrophea, has nectaries on the foliar blade in addition to petiolar nectaries.
Among species that show glands defined as EFN and verified through chemical tests for the presence of total carbohydrates [17,[28][29][30], most of them have glands that fit exclusively into the pattern I, as described in the present work. Since this morphological type is representative of EFN in Passiflora, we can denominate such pattern I glands as elevated nectaries ("Hochnektarien") according to the classification of Zimmermann [16]. In describing the structure of EFN in Passiflora species, other authors, such as Durkee [17] and Silva et al. [28], have already classified these glands as elevated nectaries. Analyzing the EFN in Piriqueta and Turnera (genera currently within Passifloraceae) Gonzales & Ocantos [31] classified most of the nectaries as elevated ones.
In pattern II, the glands that occur on abaxial surface and margin of leaf blade have a circular shape forming an ocellus, and the projection in relation to the leaf tissue is not evident to the naked eye. In this group, we mention Passiflora contracta, P. ferruginea, P. misera and P. organensis, two of which have glands exclusively on the abaxial surface of the leaf blade (P. misera and P. organensis), while the other two have petiolar glands that fall under morphological pattern I. The marginal glands included in this morphological type are present in only two of the analyzed species, P. galbana and P. odontophylla. Since this morphological pattern is also representative among the EFN of Passiflora, we classified these glands as flattened nectaries ("Flachnektarien") according to Zimmermann [16]. Durkee [17] mentioned the nectaries of the abaxial surface as embedded in the surface of the organ, a category included by Elias [11] to Zimmermann [16] classification, whereas Silva et al. [28] classified the nectaries on abaxial surface of leaf blade as pit nectaries according to the Zimmermann [16] classification. Gonzales & Ocantos [31] also placed the EFN of Piriquetta Aubl. and Turnera L. (Turneraceae, currently Passifloraceae) present on abaxial surface of leaf blade and some marginal glands among the flattened nectaries.
The nomenclature of the different glandular shapes varies among authors. The description of the glands for some species is often mentioned only as sessile or stipitate, or as concave or convex [5,10,28,30].
In this work, we are using nomenclature for gland shape based on the solid form descriptions found in Radford et al. [22] and Harris & Harris [23]. This approach facilitates comparative studies, such as ours, through nomenclatural standardization, also contributing to a more accurate and diverse definition of the variety of glandular forms found among the different Passiflora species. When analyzing EFN in several species of Piriquetta and Turnera (Turneraceae, currently Passifloraceae), Gonzales & Ocantos [31] divide the nectaries into four distinct shapes: flat (for nectaries on abaxial surface of leaf blade), as well as globose, hemispherical and cupuliform, which are related to elevated nectaries. However, we chose not to use this classification because it would have limited our ability to distinguish among the glandular shapes found in the species studied here, thus not highlighting the great variety found in Passiflora.
Anatomically, the EFN show small variations of the same pattern among the various studied species. All extrafloral glands framed as nectaries are vascularized nectaries according to the definition of Elias [11]. Anatomical analysis reveals a multi-layered secretory epidermis (in palisade), varying in number of layers, followed by two layers of secretory parenchyma cells with dense content. This number is also variable between different species and even within a single nectary. Internally, vascular bundles with phloem endings occur in a subsecretory parenchyma. These characteristics are very similar to those already described for EFN in Passiflora species [17,[28][29][30]32], despite the differences in nomenclature in some works. Durkee [17] named the nectary epidermis as "secretory tissue", which the author described as being followed by 2-5 layers of non-secretory tissue (nectary parenchyma) that separates the secretory tissue (nectary epidermis) from the vascular supply.
In Passiflora species, the secretory parenchyma contains isodiametric cells that are larger than those of the epidermis, usually more vacuolated with a dense cytoplasm and abundant calcium oxalate crystals [17,18,28]. In the species studied here, cells of the secretory parenchyma are generally larger than the secretory epidermal cells, but they may also be flatter, being found with dense vacuolar content and druses in few species, which are more abundant in the subsecretory parenchyma. In some cases, the differentiation between nectary and subsecretory parenchyma is a fine one. In this region, Jáuregui et al. [32] report that the cells have a slightly thickened wall and that they are also very compact and almost indistinguishable from the secretory epidermis. In the species studied here the difficulty of distinguishing between the secretory epidermis and the secretory parenchyma can be verified only in some glands on abaxial surface of leaf blade. Through an ontogenetic study of glands present on the abaxial surface of leaf blade, Roth [33] verified that this region originates by periclinal divisions of the subepidermal layer and that anticlinal rows do not form as in the epidermis. In the studied glands, it was possible to detect periclinal divisions of the subepidermal layer, or hypodermis, occurring not only in the glands of abaxial surface of leaf blade, but also in those of the elevated type.
In addition to the presence of EFN, as described by several authors in Passiforaceae, Solereder [15] reported the occurrence of "glandular shaggy hairs" in Passiflora and Malesherbia (currently Passifloraceae). In the genus Passiflora the author reported that these "trichomes" are restricted to some species like Passiflora clathrata Mast., P. foetida, P. lepidota Mast. and P. villosa. Solereder [15] also reported that "glandular shaggy hairs" have a multiseriate stipe. The stipe is mentioned to be variable in length, and when long, it has vascular bundles inside. The glandular "head" consists of a multi-seriated interior with elongated cells, which are the continuation of the stipe. A palisade secretory epidermis is also present, as verified for some species analyzed here classified into pattern II glands.
Killip [5] highlights that the sections Dysosmia (DC.) Killip and Dysosmioides Killip (subgenus Passiflora) have a petiole without a "true gland", although they often have gland-tipped hairs. On the other hand, in an extensive work on EFN in Passifloraceae, Cusset [34], named the structures found in P. foetida as glandular pseudo-hairs ("pseudo-poils glanduleux"). When assessing glandular development in this same species, Roth [20] concluded that they are EFN. Although the author did not mention any carbohydrate test, the presence of lipid droplets was observed in the secretory epidermis with a Sudan III test.
When analyzing Passiflora foetida cytologically and chemically, Durkee et al. [21] treated the glands of this species as resin glands. During the chemical tests, the authors did not find the presence of carbohydrates or amino acids as being secreted; however, they did react strongly with OsO4 in situ. The authors conclude that the glands present in P. foetida may represent a transition from true EFN to lipid-secreting glands, subsequently denominating them as resin glands.
The glands described in the present work as type II are small and elongated, with a cylindrical stipe, which can, after only a cursory analysis, be confused with trichomes, having an anatomical structure similar to that of glands described by Roth [20] and Durkee et al. [21]. This glandular type has been named by many authors as "glandular hairs" [2,5,8,15,34,35]. However, Roth [20] has shown that it forms as subepidermal protuberances and thus called emergences by the author.
Apart from Passiflora foetida already described as having resin glands, P. arida, P. sublanceolata and P. villosa studied in the present work have secretory glands with very similar morphological and anatomical characteristics. Also, they did not show a positive reaction to the glucose strip test, suggesting that they are structurally similar to the resin gland in Passiflora foetida.
The section Dysosmia DC. is characterized by the presence of gland-tipped hairs, and P. foetida is coated by small sticky glands and sticky hairs [2,8]. The absence of nectaries in Dysosmia species may be related to the presence of resin glands, a probable evolutionary novelty. However, this hypothesis needs to be verified in a phylogenetic context. A similar situation was reported by Conceição et al. [36], who verified that the EFN were replaced by sticky glandular hairs in a group within the Chamaecrista (Leguminosae). In the Bignonieae (Bignoniaceae) tribe, Nogueira et al. [37] verified that the evolution of glandular trichomes with viscous secretion contributes to the reduction of EFN, i.e., species with glandular trichomes have fewer EFN. The authors associate this substitution of EFN by glandular trichomes with the colonization of more arid environments, which would make the maintenance of EFN very costly for the plant, especially when considering the water availability.
In summary, this work reflects the initial stage of a much more extensive study of extrafloral secretory glands in Passiflora. The combined morphological and anatomical analyses, together with preliminary tests for the presence of glucose in the exudate of different Passiflora subgenera, suggests the occurrence of two categories of glands, resin glands and nectaries, the last one with a wide morphological diversity. The next challenges will involve determining the nectary histochemistry and ultrastructure, as well as the chemical nature of the exudate. Once the hypothesis of resin glands has been corroborated only in species of the Dysosmia section, we can think of a new interpretation of the evolution of the secretory glands in the group.