THE EXTRAFLORAL NECTARIES OF IPOMOEA LEPTOPHYLLA (CONVOLVULACEAE)

Ipomoea leptophylla Torr. (Convolvulaceae) is a sprawling dry-site morning glory with two types of extrafloral nectaries: foliar nectaries and nectaries on the outside of the sepals. Both are shown to greatly increase insect visitation to the plant. Ants visiting sepal-surface nectaries significantly decrease flower damage caused by grasshoppers and seed losses caused by bruchids. These results are similar to those for I. carnea and other plants whose extrafloral nectary-ant interactions have been studied, but differ in detail. This is the first demonstration of antiherbivore defense of a prairie plant by nectary visitors.     

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.     

The influence of extrafloral nectaries on parasitism of an insect herbivore

The extrafloral nectaries of many plants promote ant defense against insect herbivores. We examined the influence of extrafloral nectaries on the levels of parasitism of a generalist insect herbivore, the gypsy moth (Lymantria dispar L.). Larvae and pupae of the moth were collected from trees with and without extrafloral nectaries growing in the same forests in South Korea and reared to evaluate parasitism. More parasitism occurred on plants with extrafloral nectaries in seven of the nine season-long collections at the six sites and in four out of five collecting periods. Parasitism was higher on the four main genera of plants with extrafloral nectaries than on any of five main genera of plants without extrafloral nectaries. There was no difference in parasitoid richness; nine species occurred in each group, eight of which were the same. There was a positive and almost significant correlation between the abundance of plants with extrafloral nectaries and the parasitism of gypsy moth at the sites. Extrafloral nectaries may reduce herbivory by inducing more parasitism of the insect herbivores that attack plants bearing the glands.     

THE FUNCTION OF EXTRAFLORAL NECTARIES IN OPUNTIA ACANTHOCARPA (CACTACEAE)

Opuntia acanthocarpa (Cactaceae) possesses extrafloral nectaries embedded in the areoles of new reproductive and vegetative growth. The nectar secreted by these glands attracts ants and is a nutritional food source. Members of one attracted ant species, Crematogaster opuntiae (Myrmicinae), are aggressive and efficient defenders of the plants against cactus-feeding insects. The results of our study are consistent with the ant-guard hypothesis for the role of extrafloral nectaries in O. acanthocarpa. Additionally, individuals of O. acanthocarpa are well protected in comparison with those of O. phaeacantha. The latter generally possess ephemeral extrafloral nectaries and consistently maintain fewer ants.     

Extrafloral nectaries in the genus Macaranga (Euphorbiaceae) in Malaysia: comparative studies of their possible significance as predispositions for myrmecophytism

Some species of the paleotropical tree genus Macaranga (Euphorbiaceae) live in close association with ants. The genus comprises the full range of species from those not regularly inhabited by ants to obligate myrmecophytes. In Malaysia (Peninsular and Borneo) 23 of the 52 species are known to be ant-associated (44%). The simplest structural adaptation of plants to attract ants are extrafloral nectaries. We studied the distribution of extrafloral nectaries in the genus Macaranga to assess the significance of this character as a possible predisposition for the evolution of obligate myrmecophytism. All species have marginal glands on the leaves. However, only the glands of non- myrmecophytic species function as nectaries, whereas liquids secreted by these glands in myrmecophytic species did not contain sugar. Some non-myrmecophytic Macaranga and transitional Macaranga species in addition have extrafloral nectaries on the leaf blade near the petiole insertion. All obligatorily myrmecophytic Macaranga species, however, lack additional glands on the lamina. The non-myrmecophytic species are visited by a variety of different ant species, whereas myrmecophytic Macaranga are associated only with one specific ant-partner. Since these ants keep scale insects in the hollow stems, reduction of nectary production in ant-inhabited Macaranga seems to be biologically significant. We interpret this as a means of (a) saving the assimilates and (b) stabilization of maintenance of the association's specificity. Competition with other ant species for food rewards is avoided and thereby danger of weakening the protective function of the obligate ant- partner for the plant is reduced. A comparison with other euphorb species living in the same habitats as Macaranga showed that in genera in which extrafloral nectaries are widespread, no myrmecophytes have evolved. Possession of extrafloral nectaries does not appear to be essential for the development of symbiotic ant-plant interactions. Other predispositions such as nesting space might have played a more important role.     

Comparative morphology of the leaf epidermis in the genera Codonanthe (Martius) Hanstein and Nematanthus Schrader (Gesneriaceae)*

The leaf epidermis of 14 species ofCodonanthe and 10 species of Nematanthus has been examined. Species of Codonanthe section Codonanthe are geographically restricted to south-eastern Brazil, and are diploid. They possess multicellular-uniseriate nonglandular trichomes, glandular trichomes with a four-celled head and a short body, anisocytic stomata and lack extrafloral nectaries. Species of Codonanthe section Spathuliformae and Codonanthe subgenus Codonanthella are distributed from southern Mexico through Central America to north-western South America and are tetraploid. They possess unicellular non-glandular trichomes (except C. caribaea), glandular trichomes with a two-celled head (except C. caribaea) and a short body, anisocytic stomata and extrafloral nectaries (except C. caribaea). All Nematanthus species are distributed in south-eastern Brazil and are diploid (N=8). Six species of Nematanthus consistently have multicellular-uniseriate nonglandular trichomes, glandular trichomes with a four-celled head and a short (unicellular) or long (multicellular) body, anisocytic stomata and lack extrafloral nectaries. Four species of Nematanthus have multicellular-uniseriate non-glandular trichomes, glandular trichomes with a head of more than four cells and a short body, anisocytic and helicocytic stomata and lack extrafloral nectaries.     

FOSSIL EXTRAFLORAL NECTARIES,EVIDENCE FOR THE ANT-GUARD ANTIHERBIVORE DEFENSE IN AN OLIGOCENE POPULUS

Extrafloral nectaries are secretory glands, usually found on leaves, that have been shown to promote ant defense against the insect herbivores of many modem day plants. Extrafloral nectaries were found on the 35-million-year-old fossil leaves of the extinct Populus crassa from Florissant, Colorado. Extinct ant species (belonging to five still extant genera that have modem ant-guard species), and other predators and parasitoids (whose modem relatives frequent extrafloral nectaries) also lived at Florissant. The extrafloral nectaries of P. crassa (and perhaps other plants) probably operated to attract ants and/or other arthropod defenders as early as the Oligocene.     

Time‐course proteome analysis of developing extrafloral nectaries of Ricinus communis

Floral and extrafloral nectaries are unique organs that secrete energy rich chemical components, but their contribution for nectar production is largely unknown. Here, we present the first comparative proteome dataset of four developmental stages of the extrafloral nectaries from castor plant (Ricinus communis), an important biofuel crop. Respectively, from stage I—IV, we identified 626, 613, 449 and 356 proteins, respectively, summing up 882 nonredundant proteins. Surprisingly, we identified two isoforms of the potent toxin ricin, indicating that ricin expression is not limited to seeds, but it may serve a general defense purpose for the castor plant. To date, this is the most complete dataset of proteins either from floral or extrafloral nectaries, thus contributing to lay the foundations for investigations on their ecological and evolutionary importance.     

Monocots

Green nectaries have been frequently mentioned in the literature, leading to the assumption that photosynthesis of nectaries can supply the carbohydrates secreted in the nectar, especially when storage of starch is seen in the plastids in nectaries and this starch disappears during secretion. Photosynthesis in nectaries can also provide reduction equivalents for the nectar–redox cycle and energy for secretion. However, quantitative data on the photosynthetic capacity of nectaries are largely missing. Therefore, in the present study, the photosynthetic capacity of green nectaries from a range of plants was screened; 20 floral nectaries (including six septal nectaries) and six extrafloral nectaries were studied. For the screening, chlorophyll fluorescence parameters were measured as depending on photosynthetic photon flux density (PPFD). Parameters measured were basic ground fluorescence (F) and quantum yield (Y₀) of the dark adapted sample at 0 PPFD. From the light saturation curves saturating PPFD (PPFD_sat), quantum yield at saturation (Y_sat) and maximum apparent photosynthetic electron transport rates (ETR_max) were obtained. For comparison, leaves of the plants were also measured. In most cases, the performance of the nectaries was lower than that of the leaves. F was lower in 14 floral and four extrafloral nectaries (69% of total), ETR_max was lower in 18 floral and four extrafloral nectaries (85%), Y_sat was lower in 15 floral and three extrafloral nectaries (69%). In 18 floral and two extrafloral nectaries (77%) Y₀ was well below 0.8, indicating photoinhibition. In contrast, the range of ETR_max for green nectaries was 25–140 μmol m^?2 s^?1 and overlaps well with that of green tissues in general. The lower end of the range of rates of photosynthetic carbon dioxide (CO₂) uptake of sun leaves in the literature is 10 μmol CO₂ m^?2 s^?1. Taking this value for sun‐adapted green nectaries, i.e. having a PPFD_sat > 1000 μmol m^?2 s^?1, with an area of nectar tissue measured as 3–50 mm² per flower, sugar secretion related to photosynthetic CO₂ fixation in the green nectaries is estimated at approximately 0.2–3.0 μmol hexose units flower^?1 day^?1. This is compares well in order of magnitude with the range of secretion given in the literature and clearly suggests that photosynthetic activity of green nectaries can explain a significant part, if not all, of the sugar secreted. In some nectaries ETR did not saturate with PPFD. This could be attributable to spillover from photosystem II to photosystem I and cyclic photosynthetic electron transport. It is in agreement with observations in the literature and my preliminary findings that nectary plastids often lack grana thylakoids where photosytem II is located. Cyclic photophosphorylation could provide adenosine triphosphate (ATP) energy for the nectaries. This needs further investigation. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013, 173 , 1–11.     

Occurrence,structure, ontogeny and biology of nectaries inKigelia pinnata DC

The occurrence, morphology, ontogeny, structure and preliminary nectar analysis of floral and extrafloral nectaries are studied inKigelia pinnata of the Bignoniaceae. The extrafloral nectaries occur on foliage leaves, sepals and outer wall of the ovary, while the floral nectary is situated around the ovary base as an annular, massive, yellowish ring on the torus. The extrafloral nectaries originate from a single nectary initial. The floral nectary develops from a group of parenchymatous cells on the torus. The extrafloral nectaries are differentiated into multicellular foot, stalk and cupular or patelliform head. The floral nectary consists of parenchymatous tissue. The floral nectaries are supplied with phloem tissue. The secretion is copious in floral nectary. Function of the nectary, preliminary nectar analysis, and symbiotic relation between nectaries and animal visitors are discussed.     

A novel indirect defence in Brassicaceae: Structure and function of extrafloral nectaries in Brassica juncea

While nectaries are commonly found in flowers, some plants also form extrafloral nectaries on stems or leaves. For the first time in the family Brassicaceae, here we report extrafloral nectaries in Brassica juncea. The extrafloral nectar (EFN) was secreted from previously amorphic sites on stems, flowering stalks and leaf axils from the onset of flowering until silique formation. Transverse sections at the point of nectar secretion revealed a pocket‐like structure whose opening was surrounded by modified stomatal guard cells. The EFN droplets were viscous and up to 50% of the total weight was sugars, 97% of which was sucrose in the five varieties of B. juncea examined. Threonine, glutamine, arginine and glutamate were the most abundant amino acids. EFN droplets also contained glucosinolates, mainly gluconapin and sinigrin. Nectar secretion was increased when the plants were damaged by chewing above‐ and belowground herbivores and sap‐sucking aphids. Parasitoids of each herbivore species were tested for their preference, of which three parasitoids preferred EFN and sucrose solutions over water. Moreover, the survival and fecundity of parasitoids were positively affected by feeding on EFN. We conclude that EFN production in B. juncea may contribute to the indirect defence of this plant species.     

The occurrence and abundance of plants with extrafloral nectaries, the basis for antiherbivore defensive mutualisms, along a latitudinal gradient in east Asia

Abstract. The occurrence and abundance of indigenous plants with extrafloral nectaries was evaluated within local communities and regional floras along a north to south gradient from tundra in northeastern Russia (64–70°N) through temperate types in eastern Russia and Korea to subtropical vegetation in the Bonin Islands (26–27°N) south of Japan. Moving from tundra to subtropical vegetation, there is a pattern of increasing abundance of extrafloral bearing plants as a function of total plant cover (from 10.25 to 40.18%), number of species per sampled area (from 0.11 to 1.13/100 m), and proportion of species within regional floras (from 0.32 to 7.46%). There were some plants with extrafloral nectaries in all communities but their abundance varied greatly, c. 1–25% in the four northern latitudes and c. 7–70% in the subtropical region. Ants, the primary mutualists associated with plants bearing extrafloral nectaries, have a similar pattern of increasing abundance (species richness, nest density, and colony size) along the same north–south latitudinal gradient.     

Should aphids attract or repel ants? Effect of rival aphids and extrafloral nectaries on ant–aphid interactions

Among plants and herbivores, two types of conflicts occur in relation to mutualism with ants: one is competition for ant mutualism among myrmecophilous herbivores and plants, and the other is the conflict whether to attract or repel ants between myrmecophiles and nonmyrmecophiles that are damaged by ants. We investigated the extent to which two species of aphids (Megoura crassicauda and Aphis craccivora) and extrafloral nectaries on their host plant (Vicia faba var. minor) interact with one another for their relationships with ants. We designed an experiment where ants can choose to visit seedlings colonized by (1) M. crassicauda, (2) A. cracivora, (3) both aphid species, or (4) neither aphid species. Ants preferred A. craccivora to extrafloral nectaries and avoided tending M. crassicauda. We also analyzed the population growth of each aphid when it coexists with (1) ants, (2) the other aphid species, (3) ants and the other aphid species, or (4) neither of them. Under ant-free conditions, we detected an exploitative competition between the two aphid species. The ants had no significant effect on the population of A. craccivora, whereas they had negative effects on the population growth of M. crassicauda by attacking some individuals. When both aphids coexisted, M. crassicauda suffered ant attack more intensely because A. craccivora attracted more ants than extrafloral nectaries despite ant-repelling by M. crassicauda. On the other hand, the ants benefited A. craccivora by eliminating its competitor. To avoid ant attack, aphids may have been selected either to be more attractive to ants than other sympatric sugar sources or to repel the ants attracted to them. We hypothesize that competition among sympatric sugar sources including rival aphids and extrafloral nectaries is a factor restricting aphids to be myrmecophilous. Received: January 17, 2000 / Accepted: July 4, 2000     

GoNe encoding a class VIIIb AP2/ERF is required for both extrafloral and floral nectary development in Gossypium

The floral nectary, first recognized and described by Carl Linnaeus, is a remarkable organ that serves to provide carbohydrate-rich nectar to visiting pollinators in return for gamete transfer between flowers. Therefore, the nectary has indispensable biological significance in plant reproduction and even in evolution. Only two genes, CRC and STY, have been reported to regulate floral nectary development. However, it is still unknown what genes contribute to extrafloral nectary development. Here, we report that a nectary development gene in Gossypium (GoNe), annotated as an APETALA 2/ethylene-responsive factor (AP2/ERF), is responsible for the formation of both floral and extrafloral nectaries. GoNe plants that are silenced via virus-induced gene silencing technology and/or knocked out by Cas9 produce a nectariless phenotype. Point mutation and gene truncation simultaneously in duplicated genes Ne₁Ne₂ lead to impaired nectary development in tetraploid cotton. There is no difference in the expression of the CRC and STY genes between the nectary TM-1 and the nectariless MD90ne in cotton. Therefore, the GoNe gene responsible for the formation of floral and extrafloral nectaries may be independent of CRC and STY. A complex mechanism might exist that restricts the nectary to a specific position with different genetic factors. Characterization of these target genes regulating nectary production has provided insights into the development, evolution, and function of nectaries and insect-resistant breeding.     

Nutrient transfer supports a beneficial relationship between the canopy ant,Azteca trigona,and its host tree

1. Energy fluxes between ants and plants have been a focal point for documenting mutualistic behaviour. Plants can provide resources to ants through the production of extrafloral nectaries. In exchange, ants can fertilise plants through their nutrient‐ and microbe‐rich refuse. 2. Here, we test a potential facultative mutualism between the carton‐nesting canopy ant, Azteca trigona, and their host trees. Through observational and experimental approaches, this study documents how nutrient transfer provides a basis for this beneficial ant–plant relationship. 3. In a greenhouse experiment, fertilisation with sterilised refuse (i.e. nutrients only) increased seedling growth three‐fold, while the refuse with its natural microbial community increased growth 11‐fold. 4. Total root density was doubled in refuse piles compared with the surrounding area in situ. On average, refuse provides host trees and the surrounding plant community with access to a > 800% increase in N, P and K relative to leaf litter. 5. Azteca trigona preferentially nests in trees with extrafloral nectaries and on large, longer‐lived tree species. 6. Given the nutrient‐poor nature of the Neotropics, host trees probably experience significant benefits from refuse fertilisation. Conversely, A. trigona benefit from long‐term stable structural support for nests and access to nutrient‐rich extrafloral nectaries. Without clear costs to either A. trigona or host trees, it is proposed that these positive interactions are preliminary evidence of a facultative mutualism.     

MORPHOLOGY AND ANATOMY OF FLORAL AND EXTRAFLORAL NECTARIES IN CAMPSIS (BIGNONIACEAE)

The genus Campsis (Bignoniaceae), with one New World and one Old World species, is unusual among temperate plants in having five distinct nectary sites. Multiple nectaries occur at all four of the extrafloral sites (petiole, calyx, corolla, fruit), representing an advanced strategy for ant attraction. The morphology and anatomy of the extrafloral nectaries in both species are uniform for the petioles, calyces, and young fruits; those on the outer corolla lobes are of slightly different forms. The generalized structure consists of one layer of basal cells, and a one- to two-layered secretory cup. Because of their small size, there is no vascular tissue in them. The large, vascularized (phloem only) floral nectary is an annular structure subtending the ovary.     

Ant Defense Versus Induced Defense in Lafoensia pacari (Lythraceae), a Myrmecophilous Tree of the Brazilian Cerrado1

We compared the effects of ant presence at extrafloral nectaries of Lafoensia pacari St. Hil. on herbivore damage and silicon accumulation. Plants that were accessible to ants experienced lower herbivory levels over the first 3 mo of the experiment. After 3 mo, most leaves were fully expanded with inactive extrafloral nectaries; by 6 mo there was no effect of ant access on herbivore damage. Along with experiencing higher herbivory, plants in the ant‐exclusion treatment had significantly higher silicon levels in their leaves, suggesting that silicon serves as an induced defense in this ant–plant–herbivore interaction.     

Alien and native tree species having extrafloral nectaries as favorite hunting area for arboreal endemic Philippine tiger beetles (Coleoptera: Cicindelidae) in human‐disturbed habitat in Lanao del Sur Province,Mindanao, Philippines

To document a relation between abundance of arboreal, predatory tiger beetles, their ant prey, and extrafloral nectaries attracting the ants, we gathered data from more than 10 species of native and introduced trees and large, tree‐like perennial plants in Lanao del Sur Province, Mindanao, Philippines. All specimens of tiger beetles (two Tricondyla and two Neocollyris species, all endemic to the country) were noted on five tree species characterized by presence of extrafloral nectaries, including three alien/invasive and two native ones. Invasive Spathodea campanulata and native Hibiscus tiliaceus were the most inhabited ones (respectively, 56% and 19% of beetles). Presence of tiger beetles on these trees most probably depends on high abundance of ants, which are typical prey for arboreal Cicindelidae, while occurrence of ants can result from presence of extrafloral nectaries on different parts of the plants. This suggests a new mutualistic insect–plant interaction between native and invasive species.     

Sooty Mould on Hibiscus rosa‐sinensis Caused by Leptoxyphium kurandae is Associated with Extrafloral Nectaries

In August 2013, sooty mould was observed on Chinese hibiscus (Hibiscus rosa‐sinensis) in a propagation nursery in Seoul, Korea. The sooty mould initially developed at the junction between the leaf blade and leaf petiole and then dispersed along the vein on the abaxial surface. The fungal growth pattern on the plants was quite different from general sooty moulds growing on honeydew secreted by insects on the plants. On the basis of the morphological characteristics and phylogenetic analysis using the internal transcribed spacer rDNA, this fungus was identified as Leptoxyphium kurandae. A pathogenicity test was carried out to fulfil Koch's postulates. Through field observation and a pathogenicity test, we found an association between the sooty mould and extrafloral nectaries. To our knowledge, this is the first report of sooty mould caused by L. kurandae on the extrafloral nectaries of H. rosa‐sinensis.     

A macro- and micromorphological survey of floral and extrafloral nectaries in the epiphytic cactus Rhipsalis teres (Cactoideae: Rhipsalideae)

Floral and extrafloral nectaries in plants favor pollination and defense against herbivory. Despite their wide distribution in plants and differences in position, structure, and topography, their biological and systematic significance has been underutilized. This study investigated the macro- and micromorphology of floral and extrafloral nectaries in the epiphytic cactus Rhipsalis teres and reports unusual bristle-like structures (bracteoles) functioning as extrafloral nectaries in the cactus family. The floral nectary is disc-shaped embedded in the hypanthial floral cup with anomocytic stomata as secreting structures present on the epidermal nectarial tissue. Small multicellular bristle-like extrafloral nectar-secreting structures, homologues to bracts, were observed on the plants’ stems and function as bracteolar nectaries having a relatively long and continuous secretory activity throughout several stages of the reproductive structures. Both the floral and bracteolar nectaries are functional. It is possible that in the latter nectar discharge occurs though epidermal cells, which build up pressure inside as nectar accumulates, thereby ending with rupture of the cuticle to release the liquid. The nectar in both secreting structures is scentless and colorless, and the concentration from floral nectaries is slightly lower than that of the bracteolar nectaries, 70.6% and 76.4%, respectively. The relatively higher concentration in the latter might be correlated with exposure, relative humidity and water evaporation, leading to crystallization of sugars on the stem surface in a short period of time.