The ontogeny of pollinia and elastoviscin in the anther of Doritis pulcherrima (Orchidaceae)

Wolter, M., Seuffert, C. & Schill, R. 1988. The ontogeny of pollinia and elastoviscin in the anther of Doritis pulscherrima (Orchidaceae). - Nord. J. Bot. 8: 77–88. Copenhagen. ISSN 0107–055X.
The ontogeny of pollinia of Doritis pulcherrima shows some features not commonly found in other angiosperms. The cell wails of the mature pollinium are almost identical with those of the pollen mother cells, and a callose envelope is lacking during the formation of sporopollenin. This fact may be related to the absence of a clear substructure of the exine and its low resistance to acetolysis. An exine is found only at the outer tetrads of the pollinium. The pollen grains in the tetrads possess irregularly spaced cell walls. The ontogeny of elastoviscin (specialized pollenkitt) begins in the ground cytoplasm of some tapetal cells, where small droplets are surrounded by myelin-like structures. Before anthesis the droplets fuse, flow into the loculus, and attach the pollinia to the stipe, thus forming a pollinarium. In the region in front of the elastoviscin-producing cells, some cells with specialized helical wall thickenings develop.     

兰科雄蕊发育多样性研究进展

兰科是被子植物中多样性最丰富的家族,其雄蕊形态和功能分化在亚科间变化明显,是该物种多样性形成及适应性传粉生物学的研究重点。基于现有研究资料,该文初步归纳了兰科雄蕊发育多样性的主要研究内容及现状,为野生兰花资源的保护与利用提供科学依据。结果如下:(1)可育雄蕊数目的减少和花粉愈合程度的增加在兰科分子系统树上呈明显的平行演化趋势。(2)兰科雄蕊数目的减少和功能分化与早期花器官发生中存在大量的滞后和缺失、次生融合与分裂现象等密切相关。(3)花药开裂时的4类散粉单元的花粉超微形态特征在亚科、族、亚族、属和种间差异明显。(4)兰科花药散粉单元可以为单花粉粒,也可以通过花药发育过程中源自绒毡层的三类黏性物质而聚合成不同的散粉单元,包括花粉鞘、弹性黏素和其他黏性物质。(5)花药发育揭示了兰亚科的花粉小块结构主要有三类(红门兰型、树兰型和过渡型),树兰亚科的不同数目(2、4、8)和形态(全缘、浅裂、深裂、孔裂)的花粉团是由于花药原基分化出的不育隔膜组织的数目、朝向和位置而形成的。(6)兰科花药发育中,花药室数目、花药壁发育类型、绒毡层细胞核数目、不育隔膜组织分化、胞质分裂类型、小孢子四分体排列形式、花粉细胞核数目等在亚科和属间差异明显。然而,由于种类繁多,现有研究资料难以为理解兰科雄蕊发育提供清晰的线索,包括雄蕊的发育模式、散粉单元的形成机制、花药发育的胚胎学特征等。因此,有必要重视兰科雄蕊发育研究,包括扩大取样范围和利用多学科技术方法和修订兰科花形态常用术语等。     

From anther and pollen ripening to pollen presentation

The events and processes occurring between pollen maturation, opening of the anther and presentation of pollen to dispersing agents are described. In the final phases of pollen development, starch is always stored; this occurs before the anther opens. Depending on the species, this starch may be totally or partially transformed into: (a) other types of polysaccharides (fructans and rarely callose); (b) disaccharides (sucrose); (c) monosaccharides (glucose and fructose, all situated in the cytoplasm. While awaiting dispersing agents and during dispersal, polysaccharides, especially fructans, and sucrose may be interconverted to control osmotic pressure and prevent loss and uptake of water. Opening of the anther is preceded by disappearance of the locular fluid and in many cases by partial dehydration of the pollen. Pollen generally has a water content between 5 and 50%. Pollen with a high water content may or may not be able to control water retention during pollen exposure and dispersal. Pollen may be dispersed in monads or grouped in pollen dispersing units by the following mechanisms: (i). tangling of filamentous pollen; (ii). adhesion by viscous substances (pollenkitt, tryphine, elastoviscin) derived from the tapetum; (iii). common walls. When the anther opens, the pollen may be dispersed immediately, remain until dispersed (primary presentation), or be presented to pollinators in another part of the flower (secondary presentation).     

The structure and function of orchid pollinaria

Cohesive masses of pollen known as pollinia have evolved independently in two plant families — Orchidaceae and Asclepiadaceae. Yet, the bilateral symmetry of orchids has allowed a greater degree of specialization in pollination systems and a much greater diversity in the morphology of pollinaria — units comprising the pollinia(um) together with accessory structures for attachment to the pollinator. Pollinaria differ in the degree of cohesion of pollen in the pollinium, which may be soft, sectile (comprised of sub-units known as massulae) or hard. A single hard pollinium may contain more than a million pollen grains, yet pollen:ovule ratios in orchids are several orders of magnitude lower than in plants with powdery pollen due to the lack of wastage during transport to the stigma. Attachment of pollinia to the pollinator is usually achieved by means of a viscidium that adheres most effectively to smooth surfaces, such as the eyes and mouthparts of insects and beaks of birds. The stalk connecting a pollinium to the viscidium may be comprised of a caudicle (sporogenous in origin) and/or a stipe (derived from vegetative tissue), or be lacking altogether. Caudicles and stipes may undergo a gradual bending movement 20 s to several hours after withdrawal from the flower, the main function of which appears to be to reduce the possibility of geitonogamous pollination. Other mechanisms that promote outcrossing and pollen export in orchids include pollen carryover (achieved by sectile or soft pollinia), temporary retention of the anther cap, protandry and self-incompatibility (rare among orchids). Pollinaria ensure that large pollen loads are deposited on the stigma, thus enabling the fertilization of the large numbers of ovules in the flowers of Orchidaceae. Pollinaria also ensure efficient removal of pollen from the anther, minimal pollen wastage during transit, and a high probability of deposition on conspecific stigmas.     

Anther opening, pollen biology and stigma receptivity in the long blooming species, Parietaria judaica L. (Urticaceae)

Background and aimsThis paper is about pollen ecophysiology, anther opening, pollen dispersal and the timing of the male and female phases in Parietaria judaica (Urticaceae).MethodsEcophysiological (effects of different relative humidities (RHs) and osmotic relationships) and cytological methods (stigmatic receptivity, pollen viability, histology and histochemistry) were used to determine pollen and pollination features during the long blooming period of this species.Key resultsPollen is dispersed by rapid uncurling of the filament and anther opening. The filament and anther lack cells with lignified wall thickenings, which are usually responsible for anther opening and ballistic pollen dispersal. Instead, dispersal is the result of the sudden movement of the filament. Pollen is of the partially hydrated type, i.e. with a water content greater than 30% at shedding, and readily loses water, and hence viability, at low RH. Pollen carbohydrate reserves differ with season. Starchless grains germinate quickly and are less subject to water loss. Flowers are protogynous, pollen release occurring only after complete cessation of the female phase within an inflorescence.ConclusionParietaria has partially hydrated pollen which differs from typical pollen of this type because of its reduced size and the absence of callose. Because of its low water content at the time of shedding it survives better at higher RH. Dispersal and pollination are adapted to pollen features.     

The digestion of dandelion pollen by adult worker honeybees

ABSTRACT. The digestion of dandelion ( Taraxacum officinale ) pollen by adult worker honeybees ( Apis mellifera Linn.; Hymenoptera: Apidae) was initiated at the germination pores. 30 min after feeding, pollen had reached the anterior midgut and the germination pores had become swollen. This permitted further removal of protoplasm during the next 2 h of digestion as the pollen passed into the middle portion of the midgut. 3 h after feeding, pollen grains had reached the posterior midgut where some had ruptured to release both 'naked' protoplasm and masses of protoplasm but many remained intact or were only partially digested; undigested pollen grains passed unchanged to the rectum. The lipid-rich pollenkitt layer was removed from the exine during digestion. Our studies indicate that dandelion pollen was not utilized completely by honeybees.     

Pollenkitt – its composition, forms and functions

Two types of sticky pollen coat material exist in angiosperms, both produced by the anther tapetum. Pollenkitt is the most common adhesive material present around pollen grains of almost all angiosperms pollinated by animals, whereas tryphine seems to be restricted only to Brassicaceae. Tapetal cell protoplasts have different patterns of development according to the products formed during their development and degeneration. If tryphine is formed, the tapetal cell protoplasts lose their individuality at the microspore stage. If pollenkitt is formed, their contents degenerate at later stages. Cell content is totally reabsorbed, when ripe pollen is not surrounded by any gluing material. Current knowledge of pollenkitt formation, deposition on pollen grains and chemical composition are reviewed and discussed. Methods for detecting this viscous fluid are also presented. The many functions of pollenkitt, deduced from personal observations and the literature, act in the period between anther opening and pollen hydration on the stigma; they are: (1) to hold pollen in the anther until dispersal; (2) to enable secondary pollen presentation; (3) to facilitate pollen dispersal; (4) to protect pollen from water loss; (5) to protect pollen from ultra-violet radiation; (6) to maintain sporophytic proteins responsible for pollen–stigma recognition inside exine cavities; (7) to protect pollen protoplasts from fungi and bacteria; (8) to keep together pollen grains during transport; (9) to protect pollen from hydrolysis and exocellular enzymes; (10) to render pollen attractive to animals; (11) to render pollen visible to animal eyes; (12) to hide pollen from animal eyes; (13) to avoid predation of pollen through smell; (14) to enable adhesion to insect bodies; (15) to enable pollen packaging by bees and to form corbicules; (16) to provide a digestible reward for pollinators; (17) to enable pollen clumps to reach the stigma; (18) to allow self-pollination; (19) to facilitate adhesion to the stigma; (20) to facilitate pollen rehydration. Depending on the developmental program of the species, these functions may act during pollen presentation, in relation to pollinators, during pollen dispersal and when pollen reaches the stigma.     

铁皮石斛花粉块结构及发育过程的解剖学特征研究北大核心CSCD

兰科植物的有性生殖特殊,每朵花只有1个花药,且花粉有聚集成块发育的特征。为了揭示铁皮石斛花粉块的发育特征,该研究以野生铁皮石斛不同时期的花药为材料,采用半薄切片和植物组织化学方法对其发育过程进行解剖学观察分析,并对成熟花粉块进行离体培养,观察花粉管的萌发状况。结果表明:(1)铁皮石斛花药壁由1层表皮细胞,2层药室内壁细胞,1层中层细胞和1层绒毡层细胞组成。开花时,绒毡层细胞退化,中层细胞没有退化,药室内壁细胞则形成纤维状细胞壁;药室中的小孢子母细胞没有明显的胼胝质壁结构。(2)小孢子发生属同时型,减数分裂后四分体小孢子不分散,以四合花粉状态发育,并进一步连接形成花粉块。(3)在小孢子发育中,孢粉素覆盖在整个花粉块表面形成花粉外壁,但花粉块内部的花粉没有花粉外壁结构;在花粉块表面的花粉外壁上未见花粉萌发孔。(4)在花粉离体萌发实验中,具有花粉外壁的花粉块表面花粉未见萌发,仅由花粉块内部的花粉萌发出花粉管。     

Ontogenesis of monad pollen inPterostylis plumosa (Orchidaceae,Neottioideae)

Pterostylis plumosa (Neottioideae) is an orchid with monosulcate monad pollen. Tetrads may be isobilateral, decussate, tetrahedral, rhomboid or T-shaped, but all pollen grains have a similar shape. Those belonging to the same tetrads are contiguous from microspore release to opening of the anther, with the furrow oriented inwards. Sporophytic proteins are present outside the furrow. The tapetum is of the parietal type without orbicles. The increase in pollen grain size between meiosis and maturity is only three-fold. The generative cell is spherical when the pollen is mature. These features are discussed in relation to the primitive nature of the species.     

Water status and associated processes mark critical stages in pollen development and functioning

Background

The male gametophyte developmental programme can be divided into five phases which differ in relation to the environment and pollen hydration state: (1) pollen develops inside the anther immersed in locular fluid, which conveys substances from the mother plant – the microsporogenesis phase; (2) locular fluid disappears by reabsorption and/or evaporation before the anther opens and the maturing pollen grains undergo dehydration – the dehydration phase; (3) the anther opens and pollen may be dispersed immediately, or be held by, for example, pollenkitt (as occurs in almost all entomophilous species) for later dispersion – the presentation phase; (4) pollen is dispersed by different agents, remaining exposed to the environment for different periods – the dispersal phase; and (5) pollen lands on a stigma and, in the case of a compatible stigma and suitable conditions, undergoes rehydration and starts germination – the pollen–stigma interaction phase.

Scope

This review highlights the issue of pollen water status and indicates the various mechanisms used by pollen grains during their five developmental phases to adjust to changes in water content and maintain internal stability.

Conclusions

Pollen water status is co-ordinated through structural, physiological and molecular mechanisms. The structural components participating in regulation of the pollen water level, during both dehydration and rehydration, include the exine (the outer wall of the pollen grain) and the vacuole. Recent data suggest the involvement of water channels in pollen water transport and the existence of several molecular mechanisms for pollen osmoregulation and to protect cellular components (proteins and membranes) under water stress. It is suggested that pollen grains will use these mechanisms, which have a developmental role, to cope with environmental stress conditions.     

Pollen morphology of selected species from Annonaceae

The morphology of the pollen grains of 18 species representing nine genera of Annonaceae from China is described and illustrated based on observations from scanning electron microscopy (SEM). The pollen grains are small, medium-sized, large or very large, elliptic, spherical or subspherical in monads (Artabotrys, Fissistigma, Miliusa, Trivalvaria, Uvaria and most Polyalthia), tetrads (Annona, Goniothalamus, Mitrephora and Polyalthia rumphii) or octads (Disepalum). Tetragonal, tetrahedral or rhomboidal tetrads were observed in Polyalthia rumphii. Ornamentation is psilate, foveolate, perforate, rugulate, reticulate or verrucate. Most species have no visible aperture, while Miliusa balansae, Polyalthia cerasoides, Polyalthia laui, Polyalthia oblique and Trivalvaria costata have one sulcus or 1–3 pores on proximal side or globally distributed. Disepalum lagioneurum (former Polyalthia lagioneurum) bearing octads confirms its isolation from Polyalthia, which so far has been observed monad. While the isolation of Trivalvaria costata (former Polyalthia nemoralis) from Polyalthia was not supported for the similarities of pollen characters.     

Pollen grains: Why so many?

My objective is the examination of selective forces that affect pollen number. Relationships among other floral traits of animalpollinated plants, including pollen size, stigma area and depth, and the pollen-bearing area of the pollinator may affect pollen number and also provide a model to examine how change in one trait may elicit change in other traits. The model provides a conceptual framework for appreciating intra- and inter-specific differences in these traits. An equivalent model is presented for wind-pollinated plants. For these plants the distance between putative mates may be the most important factor affecting pollen number. I briefly consider how many pollen grains must reach a stigma to assure fruit set. I use pollen-ovule ratios (P/Os) to examine how breeding system, sexual system, pollen vector, and dispersal unit influence pollen grain number. I also compare the P/Os of plants with primary and secondary pollen presentation and those that provide only pollen as a reward with those that provide nectar as part or all of the reward. There is a substantial decrease in P/O from xenogamy to facultative xenogamy to autogamy. Relative to homoecious species the P/Os of species with most other sexual systems are higher. This suggests that there is a cost associated with changes in sexual system. The P/Os of wind-pollinated plants are substantially higher than those of animal-pollinated plants, and the available data suggest there is little difference in the pollination efficiency of the various animal vectors. The P/Os of plants whose pollen is dispersed in tetrads, polyads, or pollinia are substantially lower than those of species whose pollen is dispersed as monads. There was no difference in the P/Os of plants with primary and secondary pollen presentation. The P/Os of plants that provide only pollen as a reward were higher than those that provide nectar as a reward. All of these conclusions merit additional testing as they are based on samples that are relatively small and/or systematically biased.     

Pollen morphology of the Gardenieae-Gardeniinae (Rubiaceae)

Pollen grains of 107 species of 61 genera of the Gardeniinae were investigated by scanning electron and light microscopy. The subtribe is europalynous and grains occur either as monads, tetrads or massulae. Grains are porate, colporate or rarely pororate. The majority of the genera has 3-zonoaperturate pollen grains. However, deviating numbers of apertures occur in Byrsophyllum (4–8) and Pseudomantalania (4–5). Pantoporate pollen occurs in Randia . The average equatorial size (E) of monads varies between 13 μm in Anomanthodiu to 59 μm in Posoqueria . The tetrads vary from 37 μm in Casasia to 61 μm in Calochone and Euclinia . The exine is usually reticulate, but also foveolate, rugulate, perforate and psilate exine occurs in the subtribe. The thickness of the exine is only 0.3 μm in tetrad grains of Randia armata and in the pantoporate monad grains of R. ruiziana , whereas the thickest exine occurs in Posoqueria (2.8 pm) and Euclinia (2.9 μm). Tectal excrescenses are generally absent. However, three genera with pollen in tetrads, namely Euclinia, Gardenia and Oligoco-don , show this feature. Contrary to the subtribe most genera are fairly stenopalynous, but in the neotropical genera Alibertia and Randia several different types of pollen are encountered.     

An approach to the knowledge of pollen and allergen diversity through lipid transfer protein localisation in taxonomically distant pollen grains

The aim of the present study is to localise non‐specific lipid transfer proteins (nsLTPs), obtained from Rosaceae (Prunus persica (L.) Batsch) in pollen grains of taxonomically distant plants, such as Iridaceae (Aristea latifolia G.J. Lewis), Platanaceae (Platanus acerifolia (Aiton) Willd.) and Urticaceae (Parietaria judaica L.), in order to compare pollen and nsLTP diversity. A combination of transmission electron microscopy, immunocytochemical techniques, and rabbit specific antiserum against peach nsLTPs (Pru p 3) were used. Abundant labelling to Pru p 3‐like proteins was observed in the cytoplasm, walls and pollenkitt of A. latifolia pollen grains. The presence of nsLTPs associated with the pollenkitt proves that it takes part in the defence mechanism of pollen grains. The labelling was less intense in the cytoplasm and walls of P. acerifolia. Immuno‐stained gold particles were associated with the vacuoles, lipid inclusions, endoplasmic reticulum and Golgi complex. No significant labelling was found in the P. judaica pollen grains incubated with anti‐Pru p 3 polyclonal antibodies. These results indicate important variations in the nsLTPs of different pollen species. Consequently, no taxonomic relationship between pollen grains and nsLTPs could be established.     

Pollen viability of Euro‐Mediterranean orchids under different storage conditions: The possible effects of climate change

• The future impact of climate change and a warmer world is a matter of great concern. We therefore aimed to evaluate the effects of temperature on pollen viability and fruit set of Mediterranean orchids.
• The in vitro and controlled pollination experiments were performed to evaluate the ability of pollinia stored at lower and higher temperatures to germinate and produce fruits and seeds containing viable embryos.
• In all of the examined orchids, pollen stored at ?20 °C remained fully viable for up to 3 years, reducing its percentage germination from year 4 onwards. Pollinia stored at higher temperatures had a drastic reduction in vitality after 2 days at 41–44 °C, while pollinia stored at 47–50 °C did not show any pollen tube growth.
• The different levels of pollen viability duration among the examined orchids can be related to their peculiar reproductive biology and pollination ecology. The germinability of pollinia stored at lower temperatures for long periods suggests that orchid pollinia can be conserved ex situ. In contrast, higher temperatures can have harmful effects on the vitality of pollen and consequently on reproductive success of the plants. To our knowledge, this is the first report demonstrating the effects of global change on orchid pollen, and on pollen ability to tolerate, or not, higher air temperatures. Although vegetative reproduction allows orchids to survive a few consecutive warm years, higher temperatures for several consecutive years can have dramatic effects on reproductive success of orchids.

     

Pollenkitt of some monocotyledons: lipid composition and implications for pollen germination

• The composition of pollenkitt and its role in the progamic phase of reproduction are poorly understood. With the aim of extending knowledge on these topics, we chose to study two monocotyledons rich in pollenkitt, with bi‐celled and long‐lived pollen and dry‐type stigma: Crocus vernus Hill subsp. vernus and Narcissus poeticus L.
• Fatty acids of pollenkitt were assayed with gas chromatography. Germination tests were performed in vivo by pollinating the stigmas with a beard hair under a stereomicroscope, and in vitro in liquid culture medium using pollen, either treated or not, with carbon disulphide to remove pollenkitt. The pollen tube percentages were evaluated using fluorescence microscopy techniques. Scanning electron microscopy was used to examine pollen and to follow the early post‐pollination stages.
• Pollenkitt forms bridges between pollen grains but not between grains and stigma papillae. It consists of a mixture of 25 fatty acids, most with long and unsaturated chains, among which are some omega acids. The same acids with different percentages persist on the peritapetal membrane. After its removal, the pollen loses adhesiveness and dries quickly, but retains full capacity for germination on the papillae and can even trigger germination in contiguous pollen grains that do not touch the papillae.
• The results, while confirming the key role of pollenkitt in protecting pollen and favouring pollination, suggest secondary roles in the progamic phase, and highlight the interactive ability of the pollen regardless of lipid shell. The predominance of fatty acids with 18:3 and 16:0, as already noted in Brassica napus pollenkitt, suggests their hierarchy independent of plant species.

     

琼榄小孢子发生、雄配子体发育及花粉粒形态

利用光学显微技术和电镜扫描技术研究了琼榄的小孢子发生、雄配子体发育和花粉粒形态以增加广义心翼果科的胚胎学和孢粉学资料。主要结果如下：（1）花药四孢囊;（2）花药壁四层,从外到内分别为表皮、具纤维性加厚的药室内壁、退化早的中层和细胞具2~4核的分泌型绒毡层;（3）小孢子母细胞胞质分裂同时型,形成四面体型排列的小孢子四分体;（4）成熟花粉粒为二细胞型;（5）花粉粒具3个隐形萌发孔,外壁为网状纹饰。琼榄与心翼果属的小孢子发生和雄配子体发育特征非常相似,稍有不同。琼榄的花粉粒形态特征与同属其它种基本相同。     

Dioecy and wind pollination in Pernettya rigida (Ericaceae) of the Juan Fernández Islands

Pernetttya rigida is endemic to the Juan Fernández archipelago. Although all flowers are complete, with seemingly fertile stamens and pistils, differences in fruit production and detailed field, anatomical, and morphological studies indicate they are functionally unisexual, and the species is consequently dioecious. A comparison of 15 features demonstrated sigdicant differences between the sexes. The populational sex ratio is 1:1. Nectaries located between the filaments produce small amounts of floral nectar with similar sugar composition in both sexes. There are =33,357 (or = 133,429) pollen tetrads (or pollen grains)/male flower and =109 ovules/female flower. No tetrads in either hand self-pollinated or open pollinated male flowers showed any pollen germination. Tetrads on open- and hand-pollinated female flowers germinate. Female flowers do not show autogamy or apomixis. During more than 80 hours of field observation, we recorded only seven floral visitors (representing three insect species). In spite of this, openpollinated female flowers have abundant fruit and seed-set. Thus, we conclude that pollen is transferred abiotically and the ever-present wind over the exposed ridges of the islands is the likely dispersal agent. A number of anemophilous features, such as dry pollen and exposed habitat, support this conclusion. Thus, dioecy and anemophily have evolved independently, in situ , in this species in this remote locality. Preservation of habitat and elimination of competitive invasives are the primary conservation challenges.     

THE EVOLUTION OF POLLEN TETRADS IN ONAGRACEAE

In Onagraceae, pollen is shed in mature tetrads in most Epilobieae, many species of Ludwigia (Jussiaeeae), and two closely related species of the large genus Camissonia (Onagreae). Mature tetrads of Camissonia cardiophylla and representative species of Epilobium and Ludwigia were examined with light, scanning, and transmission electron microscopes. Morphological diagnoses of monad units indicated that individual taxa could be readily distinguished. Statistical analyses of tetrads which remained after acetolysis treatment revealed significant differences in the strength of the binding mechanisms. Mechanisms of tetrad cohesion were found to consist of two principal types. Common to all taxa is cohesion of pollen wall surfaces at the aperture margins; this mechanism is well known in many angiosperm groups. With the exception of Camissonia, the remaining taxa also display binding by means of short exine fragments between adjacent pollen units. These fragments, termed bridges and reported here for the first time, are located in the area extending from the aperture margins to near the center of the proximal exine faces. Thin sections reveal that layers of the bridges are identical with those of the exine. Comparisons were made between bridges and viscin threads, both of which occur on the proximal faces of the grains. Viscin threads are present on all pollen grains in Onagraceae and exhibit distinctive morphologies, and bridges were viewed morphogenetically as related to viscin threads but including an endexine layer and occupying a position near the apertures where cohesion of wall surfaces also occurs. In an evolutionary sense, the formation of mature tetrads almost certainly occurred independently in Camissonia and may have done so in Ludwigia and the Epilobieae.