MORPHOLOGY AND DISTRIBUTION OF PETIOLAR NECTARIES IN IPOMOEA (CONVOLVULACEAE)

The distribution of petiolar nectaries in 24 species of Ipomoea was investigated. Petiolar nectaries were found on 12 species (8 new reports, 4 confirmations of previous reports) and quoted from the literature as being found on 3 other species; they were absent from 9 species investigated. The structure of petiolar nectaries in the genus ranges from simple beds of superficial nectar-secreting trichomes (1 species), to slightly recessed “basin nectaries” (8 species), to “crypt nectaries,” which are structurally the most complex extrafloral nectaries known (3 species). (Structures were not determined for 3 species.) Petiolar nectaries are present in all subgenera, but all crypt nectaries occur in the same section (Eriospermum). Species with extrafloral nectaries tend to be perennial; species lacking extrafloral nectaries tend to be annual. There is no relationship between temperate or tropical habitat and presence of nectaries.     

Trichome micromorphology of Iranian Stachys (Lamiaceae) with emphasis on its systematic implication

Trichomes of 37 taxa of the genus Stachys and one species of Sideritis (S. montana) were examined using light and scanning electron microscopy. The indumentum shows considerable variability among different species, but is constant among different populations of one species, and therefore, affords valuable characters in delimitation of sections and species. The characters of taxonomic interest were presence of glandular and non-glandular trichomes, thickness of the cell walls, number of cells (unicellular or multi-cellular), presence of branched (dendroid) trichomes, presence of vermiform trichomes, orientation of trichomes in relation to the epidermal surface, curviness of trichomes, and presence of papillae on trichome surface. Two basic types of trichomes can be distinguished: glandular and non-glandular trichomes. The glandular trichomes can in turn be subdivided into subtypes: stalked, subsessile, or sessile. The stalks of the glandular trichomes can be uni- or multi-cellular. Simple unbranched and branched trichomes constitute two subtypes of non-glandular trichomes. Our data do not provide any support for separation of Sideritis from Stachys. The following evolutionary trends are suggested here for Stachys: vermiform trichomes with stellate base are primitive against vermiform trichomes with tuberculate base, long vermiform trichomes are primitive against the short simple trichomes, appressed trichomes are advanced against spreading ones, and loss of glandular trichomes is advanced against their presence. Overall, trichome micromorphology is more useful in separation of species within sections rather than characterizing large natural groups known as sections, except for few cases.     

The foliar micromorphology of Solanum pseudocapsicum

Foliar micromorphology of Solanum pseudocapsicum was investigated by electron microscopical examination. The leaves are characterized by anisocytic stomata which are more abundant on the abaxial surfaces. The leaves have short multicellular glandular trichomes sparsely distributed over the entire leaf surfaces. Crystal deposits were also observed on the surfaces above the stomata. Energy dispersive X-ray spectroscopy-SEM showed that Al, K, Na and Si were the major constituents of the crystals analyzed. The presence of glandular trichomes in this plant could be the source of poisonous compounds that are characteristic of this species.     

Trichomes and stomata,and their taxonomic significance in theUrticales

Structure and ontogeny of stomata and trichomes have been studied in 23 species and 3 varieties of theUrticales. Stomata are anomocytic, more rarely paracytic; anisocytic and sometimes helicocytic and transitorial types are found inUrticaceae andDorstenia, rarely inArtocarpus. The ontogeny of anomocytic and actinocytic stomata is perigenous, of paracytic either mesogenous or perigenous, of anisocytic either mesogenous or mesoperigenous, and of helicocytic and transitional types mesogenous. Among trichomes eglandular unicellular (wide spread), bicellular or uniseriate filiform (Cannabis); glandular capitate with uni- or bicellular (Moraceae, Ulmaceae, Cannabaceae), uniseriate filiform (Ulmaceae) or multiseriate stalk (Cannabis); sunken glands (Artocarpus); uniseriate glandular with uniseriate stalk (Celtis), and stinging emergences (Urticaceae) have been observed. It is concluded that theUrticales represent a natural order with four families:Ulmaceae, Moraceae, Urticaceae andCannabaceae which are distinct but interrelated with each other.     

Is nectar reabsorption restricted by the stalk cells of floral and extrafloral nectary trichomes?

Reabsorption is a phase of nectar dynamics that occurs concurrently with secretion; it has been described in floral nectaries that exude nectar through stomata or unicellular trichomes, but has not yet been recorded in extrafloral glands. Apparently, nectar reabsorption does not occur in multicellular secretory trichomes (MST) due to the presence of lipophilic impregnations – which resemble Casparian strips – in the anticlinal walls of the stalk cells. It has been assumed that these impregnations restrict solute movement within MST to occur unidirectionally and exclusively by the symplast, thereby preventing nectar reflux toward the underlying nectary tissues. We hypothesised that reabsorption is absent in nectaries possessing MST. The fluorochrome lucifer yellow (LYCH) was applied to standing nectar of two floral and extrafloral glands of distantly related species, and then emission spectra from nectary sections were systematically analysed using confocal microscopy. Passive uptake of LYCH via the stalk cells to the nectary tissues occurred in all MST examined. Moreover, we present evidence of nectar reabsorption in extrafloral nectaries, demonstrating that LYCH passed the stalk cells of MST, although it did not reach the deepest nectary tissues. Identical (control) experiments performed with neutral red (NR) demonstrated no uptake of this stain by actively secreting MST, whereas diffusion of NR did occur in plasmolysed MST of floral nectaries at the post‐secretory phase, indicating that nectar reabsorption by MST is governed by stalk cell physiology. Interestingly, non‐secretory trichomes failed to reabsorb nectar. The role of various nectary components is discussed in relation to the control of nectar reabsorption by secretory trichomes.     

Trichome complement of Turnera and Piriqueta (Turneraceae)

The indumentum of Piriqueta and Turnera is made up of nine different types of trichomes, which broadly can be divided into glandular and non-glandular. Taking into account foot shape, head size and pedicle size, five variants of glandular trichomes are recognized: microcrapitate, stipitate-capitate, sessile-capitate and setiform. The non-glandular trichomes can be simple (unicellular or pluricellular-uniseriate), stellate or porrect-stellate. The setiform glandular hairs are present in most species of Piriqueta . Simple unicellular hairs are the most widespread type, frequently being found in combination with other trichomes. Stellate trichomes show a restricted distribution in both genera. Within Piriqueta , section Africana has only simple trichomes, whereas section Piriqueta has also porrect-stellate trichomes; groups of species can be set up according to the presence and type of glandular trichomes. Within Turnera the stipitate-capitate trichomes are exclusive to series Papilliferae ; sessile-capitate trichomes are found in series Microphyllae , Annulares and in some species of Salicifoliae ; clavate trichomes are found only in series Turnera ; setiform glandular hairs are exclusive to T. collotricha , whereas the microcapitate trichomes are widely distributed.  © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 144 , 85–97.     

Ficus carica L. leaf anatomy: Trichomes and solid inclusions

Ficus carica L., a typical plant of the Mediterranean environment, presents leaves covered by an extensive indumentum, and a mesophyll full of solid inclusions. The morphology and ultrastructure of the trichomes, calcium carbonate cystoliths and silicified structures of leaves of F. carica cv Dottato were investigated with light, confocal, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. At the same time, histochemical reactions were also employed to analyse the indumentum composed by glandular and non-glandular trichomes by applying chemical reagents and fluorescence microscopy. Non-glandular and glandular trichomes, capitate, are described. Non-glandular trichomes are unicellular simple, spine-like and present different morphology and sizes. The capitate glandular trichomes are present on leaf adaxial and abaxial surface and consist of one-celled stalk and 3/4 cells spherical head. Histochemical characterisation of leaf hairs revealed the presence of flavonoids, while glandular trichome head cells showed a complex mixture of alkaloids, essential oil and flavonoids. Cu and Al were found in the constitutive structures, spike and dome, of the cystoliths. Several epidermal cells and non-glandular trichomes were silicified. Leaf hairs, trichomes secretions, solid inclusions and silicification of F. carica leaf have significant roles to play in relation to leaf protection from external factors, including high-intensity radiation, herbivores or pathogens.     

Trichome morphology provides phylogenetically informative characters for Tremandra, Platytheca and Tetratheca (former Tremandraceae)

Summary Trichomes of Tremandra R.Br. ex DC., Platytheca Steetz and Tetratheca Sm. (Elaeocarpaceae, former Tremandraceae), together with two outgroup species of Elaeocarpus L., are illustrated using scanning electron microscopy, and their distribution on various plant organs is documented. Various trichomes types were identified that relate taxa: simple hairs, stellate hairs, short glandular trichomes, long glandular trichomes, and three forms of tubercules. Both outgroup and ingroup taxa have simple hairs. Stellate hairs are confirmed as unique to Tremandra. Prominent and sculptured multicelled tubercules, some bearing a stout hair, are characteristic of Platytheca. Smaller multicelled tubercules occur in both Platytheca and Tetratheca, except for the Western Australian taxon Te. filiformis Benth. (possibly plesiomorphic). Unicellular tubercules (papilla) characterise two species of Tetratheca. Short glandular trichomes, usually found on the ovary, also occur in both of these genera but not in all species (possibly secondary losses), while long glandular trichomes, usually on stems and leaves, occur only in some groups of Tetratheca. Within Tetratheca, Western Australian taxa that have five-merous flowers fall into three ‘groups’: seven species (together with one from South Australia) that have short glandular trichomes but no long glandular trichomes; six species that have long glandular trichomes but no short glandular trichomes; and four species that have both trichome types. All other species of Tetratheca have four-merous flowers and form two ‘groups’: 12 eastern species (including one from South Australia) that have both short glandular trichomes and long glandular trichomes; 4 western species and six eastern species that lack short glandular trichomes. On the basis of these characters, a phylogenetic hypothesis for the three genera is presented.     

Colleters in Turnera and Piriqueta (Turneraceae)

The anatomy of colleters was examined by light and scanning electron microscopy in 25 species of Turnera and nine species of Piriqueta. Based on morphology, four categories of colleters were recognized: standard, sessile, lachrymiform and trochleariform, all of which differ in shape and length/width ratio. They all have a similar anatomy: they consist of an axis of parenchymatous cells, sheathed by a palisade epidermis. The standard type is the most widespread in the studied taxa; the lachrymiform example was found in those species of Piriqueta with setiform glandular hairs; only one trochleariform example appeared in T: diffusa. The sessile type is considered to be a morphological transitional form between extrafloral nectaries and colleters. This is the first record of sessile, lachrymiform and trochleariform colleters. The anatomy of colleters is compared with other secretory structures such as glandular trichomes and extrafloral nectaries.     

Glandular trichomes and essential oil constituents ofCalamintha menthifolia (Lamiaceae)

Plant material ofCalamintha menthifolia was collected from two populations grown in the Vikos-Aoos area (NW. Greece). The structure and ontogeny of the glandular trichomes and the chemical composition of the secreted essential oil were studied. The leaves ofC. menthifolia have numerous glandular trichomes of three morphological distinct types: 1) glandular scales with a unicellular foot and stalk, and a 12-celled head, 2) glandular hairs with a unicellular foot and stalk, and a unicellular pear-shaped head and 3) glandular hairs with a unicellular foot, a bicellular stalk and a unicellular elongated head. Qualitative and quantitative GC-MS analyses of the essential oils revealed piperitone oxide as the main constituent in both populations. In the light of these results the relationships beweenC. menthifolia and other members of theSatureja group as well as its taxonomy are discussed.     

Anatomy and histochemistry of the nectaries of Rodriguezia venusta (Lindl.) Rchb. f. (Orchidaceae)

Orchidaceae is one of the largest angiosperm families. Although extensively studied, reports of anatomy of secretory structures of orchids are relatively scarce. Rodriguezia venusta is an epiphytic orchid occurring in Brazil and Peru that has floral and extrafloral nectaries. This study describes the structure and the histochemistry of these secretory structures. Floral and extrafloral nectary samples were obtained from R. venusta plants that were collected in a gallery forest in the State of Bahia, Brazil, and grown in a greenhouse. Theses samples were fixed and processed according to routine procedures in plant anatomy and histochemistry or for scanning electron microscopy. The extrafloral nectaries occur on the edge and sub-edge of young leaves and at the basal portion of bracts that subtend the floral buds. They are structurally very similar, being formed by a nectary parenchyma and a simple epidermis with stomata (“non-structured nectaries”). The floral nectary is inserted at the floral receptacle fused with the labellum base, between this structure and the two inferior connate sepals. This nectary consists of an epidermis with numerous specific nectar secreting trichomes, a subnectary and a nectary parenchyma abundantly supplied by vascular terminations. Its structure is complex and distinct from other floral nectaries described for Orchidaceae.     

An investigation of the foliar trichomes of Tetradenia riparia (Hochst.) Codd [Lamiaceae]: An important medicinal plant of Southern Africa

The morphology and distribution of leaf trichomes of Tetradenia riparia were studied using light and scanning microscopy. Three morphologically distinct types of trichomes were observed on T. riparia leaf surfaces: glandular capitate (short and long stalked), peltate and non-glandular. The glandular and non-glandular trichomes were present in abundance on both the adaxial and abaxial surfaces. Young leaves were densely covered with trichomes; however, the density of trichomes decreases progressively with leaf maturity. This suggests that the trichomes are established early in leaf differentiation and their density decreases with leaf development and age.     

Glandular Trichomes on Alfalfa Impede Searching Behavior of the Potato Leafhopper Parasitoid

New cultivars of alfalfa, Medicago sativa L., have been released with glandular trichomes for resistance to potato leafhopper, Empoasca fabae (Harris). Yet, the impact of the glandular trichomes on the primary natural enemy of the leafhopper, Anagrus nigriventris Girault, is unknown. We compared the host searching behavior of the egg parasitoid on four alfalfa clones varying in trichome characters. Female wasps were videotaped on Ranger, a susceptible clone with relatively sparse trichomes, B14, a resistant clone with dense but nonglandular trichomes, and FG12 and FG18, two resistant clones with glandular trichomes. Although the number of leafhopper eggs per stem exposed to wasps did not significantly differ among the four clones, the frequency of foraging and total foraging time were less on the two clones with glandular trichomes than on the two clones with nonglandular trichomes. In addition, an analysis of covariance demonstrated that, although the number of ovipositional probes increased with egg density on a stem, the number of probes on stems with glandular trichomes was significantly less than that on stems without glandular trichomes. The allocation of time by wasps among drumming, probing, and grooming behaviors was similar among the clones. Wasps tended to fly off of clones with glandular trichomes more often than off of clones with nonglandular trichomes. This study suggests that cultivars with glandular trichomes may interfere with host searching by A. nigriventris.     

Glandular Trichomes on Vegetative and Reproductive Organs of Leonotis leonurus (Lamiaceae)

The types of glandular trichomes, their ontogeny and patternof distribution on the vegetative and reproductive organs ofLeonotis leonurus at different stages of development, are studiedby light and scanning electron microscopy. Two morphologicallydistinct types of glandular trichomes (peltate and capitate)are described. Peltate trichomes, at the time of secretion,are characterized by a short stalk, which is connected witha large spherical head composed of eight cells in a single layer.Capitate trichomes can be divided into various types. Generally,they consist of a four-celled head supported by one or threestalk cells. The two kinds of trichomes differ in the secretionprocess. In the peltate trichomes, the secretory product seemsto remain accumulated in a subcuticular space, unless an externalfactor damages it. In the capitate trichomes, this product probablybecomes released through micropores. On the leaves peltate andcapitate trichomes are abundant, while on the flowers only thepeltate trichomes are numerous and the capitate are rare orabsent.Copyright 1995, 1999 Academic Press Leonotis leonurus R. Br., lion's ear, lion's tail, Lamiaceæ, glandular trichomes, morphology, ontogeny     

冬凌草腺毛的形态学及组织化学研究

利用光学显微镜对药用植物冬凌草地上部分腺毛的形态、分布和组织化学进行了研究。结果表明:(1)冬凌草的叶表皮有3种形态显著不同的毛,即非腺毛、盾状腺毛和头状腺毛;盾状腺毛和头状腺毛均具1个基细胞、1个柄细胞和头部;成熟的盾状腺毛的头部一般由4个分泌细胞组成,而头状腺毛头部由2个分泌细胞组成。(2)组织化学鉴定结果显示:2种腺毛中均含有黄酮类成分,盾状腺毛中还含有单萜、倍半萜等萜类成分;冬凌草甲素可能只存在于盾状腺毛中,但需要更直接的证据证明。研究认为,高密度的盾状腺毛可以作为筛选冬凌草高甲素含量品种的一项重要依据。     

Trichome micromorphology of the East Asiatic genus Chelonopsis (Lamiaceae) and its systematic implications

The micromorphology of trichomes of the leaves of 17 taxa (including two varieties) of the genus Chelonopsis Miq. and of six species representing four additional genera (Bostrychanthera deflexa Benth., Colquhounia coccinea Wall. var. coccinea, Co. seguinii Vaniot. var. seguinii, Gomphostemma chinense Oliv. var. chinense, G. crinitum Wall. ex Benth. and Physostegia virginiana (L.) Benth.) was surveyed by light and scanning electron microscopy. Two basic types of trichomes can be identified: non-glandular and glandular trichomes. The non-glandular trichomes can be subdivided into two subtypes: simple unbranched and branched trichomes. Based on the cell number, simple unbranched trichomes are further divided into four shapes (unicellular, two-celled, three-celled, and more than three cells), whilst branched trichomes are separated into three shapes (biramous, stellate, and dendroid trichomes). The glandular trichomes can in turn be subdivided into four subtypes: subsessile, capitate, clavate, and sunken. Non-glandular trichomes with two cells (NGTW) and subsessile glandular trichomes (GSU) are most widespread in all taxa examined. The indumentum shows considerable variation among different sections or species. Consequently, trichome micromorphology and distribution have high taxonomic value for Chelonopsis at both infrageneric and interspecific levels. The presence of capitate glandular trichomes (GCA) provides an additional morphological character to clarify the boundaries between subgenus Chelonopsis and Aequidens Wu and Li. Within subgenus Aequidens, non-glandular trichomes with more than three cells (NGMT) and clavate glandular trichomes (GCL) are important characters for sectional division between sect. Aequidens Wu and Li and sect. Microphyllum Wu and Li. Again, three forms of three-celled trichomes can be used as a distinctive taxonomic character at specific level between C. albiflora Pax et K. Hoffm. ex Limpr., C. forrestii J. Anthony, and C. souliei (Bonati) Merr. in sect. Aequidens. This study supports Wu's delimitation of subgenus and sections and the subsequent review work by Xiang et al. Additionally, distribution of trichome types is correlated with the altitudinal distribution and habitats of some species in Chelonopsis.     

Influence of elevated CO2 and ultraviolet-B radiation levels on floral nectar production: a nectary-morphological perspective

 Investigations of the effects of two global events – elevated CO₂ levels and enhanced ultraviolet-B (UV-B) radiation – on floral nectar production are reviewed from twelve dicotyledonous families. Furthermore, to allow comparisons between nectary morphology and nectar production in treated plants of these fifteen species, new data on floral nectary structure are provided for Malcolmia maritima (L.) R. Br. (Brassicaceae) and Scabiosa columbaria L. (Dipsacaceae). All but the last taxon possessed mesenchymatic floral nectaries with surface stomata. Few clear relationships existed between nectary morphology and various physiological responses to CO₂ or UV-B enrichment, indicating that species responded notwithstanding nectary structure itself. Overall, nectar-solute concentration was least affected by elevated CO₂ or UV-B radiation; consequently, changes in nectar volume were responsible for differences in nectar-sugar production per flower. Three species of Fabaceae experienced no change in floral nectar production upon exposure to elevated CO₂. To date, no study of enhanced UV-B radiation reported a consistent reduction in floral nectar production; three species of Brassicaceae responded differently, but various levels of ozone depletion were simulated. Experimentation with more taxa – including those possessing nectary types such as septal (gynopleural) nectaries (e.g. many monocotyledons) or aggregations of glandular trichomes – and expanding such physiological studies to species possessing extrafloral nectaries, are recommended. Received August 8, 2002; accepted November 23, 2002 Published online: June 2, 2003     

A Study on the Morphology of Foliar Trichomes of Evergreen Oaks (Quercus) in China and Its Implication in Taxonomy

Most of the evergreen oaks (Quercus L.) are endemic to China and distributed in a large moutainous area of southwestern China at an altitude of 2600-4000m. The delimitation of sections and species in the group has not been satisfactorily solved. The foliar trichomes are very an important character in identifying species of oaks. As a result of observation on 17 species and 2 varieties of evergreen oaks in China under scanning electron microscope, ten types of foliar trichomes are recognized: Simpleuniseriate, Simple-branched, Bulbous, Rosulate, Solitary, Stipitate-fasciculate, Fasciculate, Multiradiate, Stellate and Fused-stellate. The first four types fall into glandular trichomes and the last six non-glandular trichomes. The taxa examined have a combination of various types of the trichomes. All the evergreen oaks have non-glandular trichomes on their foliar epidermis, but glandular trichomes occur solely in certain taxa. These two types of foliar trichomes are obviously different in structure and function, which represent different adular trichomes and the last six non-glandular en oaks are divided into two groups: the glandular group and the non-glandular group according to the types of foliar trichomes and it is reasonable to divide the evergreen oaks into two sections: Sect. Suber (Reichenb.) Spach and Sect. Englerianae (A. Camus) Hsu et Jen. Foliar trichomes of the evergreen oaks show a continuity in density from species predominately with glandular trichomes at a high altitude to species solely with non-glandular trichomes at a low elevation. The characters of branching of foliar trichomes, especially the number of branches, can imply to some extent the evolutionary position of a given evergreen species. Considering the types, density and branches of foliar trichomes combined the evolutionary relationships among the evergreen oaks in China are proposed. Q. gilliana is the startpoint, from where evolution took place in two directions: glandular and non-glandular. In the glandular direction envolved are Q. aquifolioides, Q. longispica and Q. guyavaefolia. Q. pannosa is a species with the most types and highest number of glandular trichomes. In non-glandular line aligned are Q. spinosa, Q. senescens, Q. senescens var. muliensis, Q. monimotricha with the reduction of glandular trichomes and increase of non-glandular trichomes. After Q. tungmaiensis no glandular trichomes appear and it solely depends on non-glandular trichomes to protect itself. Q. granchetii is the climax in the non-glandular line with the highest density and number of branches of foliar trichomes. And then some species, such as Q. engleriana, Q. phillyraeoides, have few or no trichomes. Q. dolicholepis, Q. baronii and Q. baronii var. capitata show the close re-lationships because they share fused-stellate trichomes.     

The taxonomic value of leaf anatomy and trichome morphology of the genus Cyclotrichium (Lamiaceae) in Turkey

The genus Cyclotrichium (Boiss.) Manden. & Scheng. is represented by six species in Turkey: C. glabrescens, C. leucotrichum, C. longiflorum, C. niveum, C. origanifolium and C. stamineum. They are aromatic perennial subshrubs used as spices or herbal teas in traditional Turkish medicine. The leaf anatomy and tomentum morphology of leaves and calyces of Cyclotrichium species in Turkey was investigated by scanning electron microscopy (SEM) and light microscopy (LM). The investigated species have equifacial (C. niveum, C. origanifolium) or bifacial leaves (C. glabressens, C. leucotrichum, C. longiflorum, C. stamineum). All species have peltate and capitate glandular, and simple (all species) or branched (C. niveum) eglandular trichomes and diacytic stomata. Peltate trichomes consist of a basal cell embedded in the epidermis, a stalk cell, and a broad 12 (–13)‐celled secretory head arranged in two concentric circles. The capitate trichomes observed in Cyclotrichium can be grouped into five types, differing in structure and size. They consist of either a pear‐shaped or globose unicellular head and uni‐or bicellular stalk, or a bicellular head and bicellular stalk. The density of peltate, capitate and eglandular trichomes differs between species. Peltate trichomes are densely spaced only on the calyx and on the leaf surface of C. niveum and C. origanifolium and on the abaxial leaf surface of C. longiflorum and C. stamineum. The significance of trichome architecture for taxonomy in Cyclotrichium and Lamiaceae in general is discussed.     

Leaf anatomy ofDombeya andNesogordonia (Sterculiaceae), emphasizing epidermal and internal idioblasts

We studied leaf anatomy, using clearings, resin sections, and scanning electron microscopy, from mostly herbarium specimens of 123 species ofDombeya and 11 species ofNesogordonia (Sterculiaceae). Species were placed in seven idioblast categories, ranging from those without any to single and bicelled epidermal forms to multicelled nodules and single mesophyll idioblasts. Idioblast contents are possibly mucilaginous, but were not identified. In these two genera the range of foliar idioblast morphology surpasses that known previously for the entire family. Leaves are dorsiventral with mostly abaxial anomocytic stomata and typical palisade and spongy layers; paraveinal mesophyll is lacking. Miniature glandular (clavates, capitates) and nonglandular (mostly stellate) trichomes occur. Prismatic crystals predominate; epidermal prismatics and mesophyll druses are rare.