A light, scanning electron, and transmission electron microscopic study of pollen wall architecture in the subtribe Gnaphaliinae (Gnaphalieae, Asteraceae)

To better understand relationships within the Asteroideae, the pollen morphology and exine structure of 10 genera and 15 species of Gnaphaliinae were investigated using light, scanning electron, and transmission electron microscopy. All taxa have a Gnaphalioid pattern of exine with an evidently rough foot layer. The tectal complex consists of three main layers that differ in morphology and thickness: a tectum, a median columellar layer, and an internal interlaced sub-columellar layer. The apertural system consists of an ectoaperture, a mesoaperture, and an endoaperture, which intersect, respectively, the tectal complex, the foot layer and the upper part of the endexine, and the inner part of the endexine. On the basis of pollen characteristics, especially those of the spines, all the species examined may be gathered into two groups, one including Helichrysum foetidum, H. italicum, Plecostachys serpyllifolia, and Pseudognaphalium luteo-album and the other including the other 11 species of Gnaphaliinae now investigated. In addition, because Gnaphalieae has been proposed as sister group to several tribes and clades of Asteroideae, a comparison was made between exine pattern in the Gnaphalieae and that in its putatively related tribes. On the basis of previous phylogenetic studies and our present pollen data we suggest that either Astereae, Astereae-Anthemideae clade, or Heliantheae s.l.-Anthemideae clade are the best candidates for the sister taxon/sister group of Gnaphalieae.     

Caractères ultrastructuraux du pollen de quelques Podostémales. Affinités avec les Rosidae évoluées

The order Podostemales are two pantropical families of aquatic plants living in running water: Tristichaceae (five genera, ten species) and Podostemaceae (35 genera, 200 species). Pollen of the 26 genera and 62 species studied is characterized by: a granular infratectum in which the granules are sometimes organized as columellae like units, and a lamellar and/or granular endexine in all pollen types, single or in dyads. Most of the apertural characters and the ornamentation of the exine allow us to distinguish the previously established taxonomic groups: Weddellinoideae have tricolporate rugulo-areolate, pollen with a smooth apertural membrane; in Tristichoideae, pollen is periporate and the microspines of the tectum and of the apertural membrane are massive; in Podostemaceae, the tectal spines with their broad bulbous base are formed from numerous masses of sporopollenin, the endexine is microfibrillar at the base, the apertural membrane is constituted of structured ectexinous masses, and the endexine is granular at the aperture. Presence of the tricolporate pollen type associates the Podostemales with the higher eudicotyledons. Most of the pollen characters of Podostemales and their variations are found among advanced Rosidae (Hamamelidales, Polygalales, Santalales, Violales, Euphorbiaceae).     

Pollen morphology of the subtribe Cuspariinae (Rutaceae)

The neotropical subtribe Cuspariinae (Rutaceae) comprises as many as 26 genera and over 125 species. Pollen grains from 111 collections representing 71 species and 24 genera were examined by LM, SEM, and TEM. The pollen morphology of this subtribe is very diverse. Grains are mostly 3–6-aperturate and colporate, rarely porate (Spiranthera) or pantocolporate (Almeidea). Exine sculpturing is most commonly reticulate, sometimes perforate, foveolate-perforate, foveolate, foveolate-reticulate, reticulate, striate-reticulate, echinate, clavate, or baculate. The exine structure is columellate and tectate-perforate, columellate and semitectate, or intectate and is stratified into ektexine and endexine. The exine ofLeptothyrsa is distinctive in that the ektexine of the mesocolpium is longitudinally deeply ridged. The pollen ofHortia, characterized by a psilate exine with rare perforations, a very thick foot-layer, and reduced columellae, is unlike that of any member of the Cuspariinae and offers no support for the transfer of this genus from the Toddalioideae. The pollen data correlate with macromorphological characters and are taxonomically useful.     

Notes on the morphology and fine structure of the exine of some pollen types in dipterocarpaceae

The pollen morphology of nine species belonging to six genera of Dipterocarpaceae is described in detail with light, scanning electron and transmission electron microscopy, while additional data on twenty-eight species are briefly discussed. In Dipterocarpoideae, grains are tricolpate and the exine consists of a thin, often laminated basal layer and an outer, sculptured layer in which columellae and tectum may either be recognizable or fused into a tilioid structure. The surface of the tectal ridges often show a highly characteristic grooved or crenelated microsculpture. In Monotoideae the grains are tricolporate and four layers can be recognized, the inner two being probably equivalent to endexine s.s. and footlayer, the outer two forming a fairly coarse tilioid reticulate sculpture.The evolutionary relations between the pollen types and their relations to taxonomy, wood anatomy and fruit morphology are discussed. A fair amount of correspondence is obvious, although discrepancies, especially with anatomical evidence, exist also.     

Comparative pollen morphology and ultrastructure of Mentheae subtribe Nepetinae (Lamiaceae)

This study provides new pollen data of 52 representative species belonging to all 12 genera in the currently classification of the subtribe Nepetinae, and considers the possible presence of orbicules for the first time. Pollen morphology and ultrastructure were investigated with light, scanning electron and transmission electron microscopy. Nepetinae pollen is small to large (P = 16–65 µm, E = 17–53 µm), oblate to prolate (P/E = 0.7–1.6) in shape and mostly hexacolpate (sometimes octocolpate). The exine stratification in all taxa studied is similar and characterized by unbranched columellae and a continuous, granular endexine. Sexine ornamentation in the Nepetinae is bireticulate, microreticulate or perforate. In perforate and microreticulate pattern a tendency towards a bireticulum could be recognized due to trace of secondary tectal connections. The bireticulate pattern is most common with variations of primary muri and secondary reticulum. In Hymenocrater and Schizonepeta the observed variation of sexine ornamentation is particularly valuable at the generic level. Pollen data support Lophanthus and Nepeta as very closely allied and Lallemantia is clearly distinct from Dracocephalum. The formerly suggested infrageneric relationships within Dracocephalum and Nepeta are only partly corroborated by palynological characters. Orbicules are absent in the Nepetinae.     

Development of the pollen wall in Tsuga canadensis (Pinaceae)

In discussions of exine structural types, Tsuga is often mentioned as an exception, since no infratectal layer is present in the ektexine. The present investigation documents the formation of this pollen wall type at the ultrastructural level in T. canadensis . All layers of the exine are formed during the tetrad period, when the microspores are surrounded by a callose wall. The outer layer (ektexine) is elaborated on a fibrillar microspore surface coat, while the inner layer (endexine) is elaborated on lamellated structures. The deposition of the pretectum is followed by the appearance of endexine lamellae. In the initial stages, the two layers—pretectum and endexine—appear to be separated from each other only by a dense microspore surface coat. As additional wall materials are deposited, the tectal elements become convoluted and come to rest, in places, on the now recognizable footlayer. Upon release from the tetrad, intine formation begins and continuous accumulation of sporopollenin leads to an increase in ektexine thickness. The mature pollen wall of Tsuga canadensis , with a convoluted tectum resting directly on the footlayer, is characteristic of the genus.     

Ontogeny of the exine in pollen of Aristea (Iridaceae)

The ontogeny of the pollen wall was studied in four species of Aristea , from the vacuolated stage of the microspores, to observe the possible formation of an endexine. At this stage, the ectexine is completely formed (tectum, columellae, and structurally homogeneous foot layer), but its maturation is incomplete and variable depending on the species. In all cases, there are one or several tripartite lamellae with a white line under the foot layer, in the apertural and extra-apertural regions. In A. major , and A. pauciflora , the exintine is not yet present, whereas in A. macrocarpa and A. glauca , it has started to initiate. In mature pollen of the four species, the tripartite endexine lamellae of the vacuolated stage disappear and there is no trace of endexine. The tripartite intine is completely formed. Maturation of exine is complete and it appears homogeneous and of medium electron density, except in A. glauca , which has particularly fragile exine, where it remains incomplete with a granular and highly electron dense appearance, which contrasts with the usually mature exine. Despite the very clear presence of endexine lamellae at the vacuolated stage, it is thus very difficult to conclude that endexine exists in pollen of the genus Aristea .     

Ontogeny of pollen in Poinciana (Leguminoseae). II. Microspore and pollen grain periods

Our interpretations for development of exine form in Poinciana gilliesii Hooker are correlated with information, published separately, on the initiation and sequence of development of the exine template. The exine develops exactly in accordance with the template in the following respects: attachment position of foot layer rods, size of the rod components of the foot layer, size of tectal components on the aperture, height of bacules both on aperture and interaperture, and craggy inner surface of the interapertural tectum. Thickness of the interapertural tectum increased after the tetrad period, and the entire endexine was formed only subsequently.The endexine, we find, consists of tubules. The central core of these tubules is low in contrast and has a diameter similar to the thickness of the “white line lamellation” common for these endexine components as seen in oblique and longitudinal views.The bacules over the entire exine, including the extensive synaperture and its prominent margin, are all about the same height. The synaperture is marvellously adapted to accommodate contraction and expansion. Each bacule is cross-connected at the top by tectal straps long enough for rather great separation of neighboring bacules and flexible enough to be folded for close packing of bacules. At their base bacules are attached to one or several rods of the endexine. These rods are either entirely separate or can become separated over apertures.     

The Pollen Morphology and Exine Ultrastructure of Paeonia L in China

The pollen morphology of 9 species of Paeonia L. has been investigated with both light microscope and scanning electron microscope. In addition, the exine structure of pollen grains of Paeonia suffruticosa and P. lactiflora was examined by transmission electron microscope. Tricolporoidate aperture is an important character of the pollen grains of the Paeonia. The surface of the exine is characterized by reticulate, foveolate and irregularly tuberculate-foveolate sculpture under the SEM. Thin sections of the pollen of this genus shows that the layers of exine are complete i.e. a perforate rectum to semitectum, columellae and foot layers. The endexine is continuous, considerably thickened in the aperture areas and relatively thin or indistinct in the mesocolpia. Paeonia has been placed in Ranunculaceae. But since the beginning of this century many authors have suggested to separating Paeonia from Ranunculaceae. Pollen marphology supports such separation. In Ranunculaceae most pollen grains are tricolpate or have other types of aperture, and exine with spinules and perforations between them. In electron microscopy, the ektexine contains a foot layer, columellae, and perforate rectum, the columellar layer with two types of columellae; the endexine is generally thin. However, the columellar layer of Paeonia has only monomorphic columellae. Some authors considered that there is a close relationship between Paeonia and the Dilleniaceae, but these also differ in the characters of the pollen grains. In Paeonia the constriction of the colpus in equator is in some degree similar to that of Theaceae (Camellia sasanqua Thunb.), Guttiferae (Hypericum L.), Actinidiaceae and Rosaceae. But in the other respects they are quite different. In sum, the pollen morphology of Paeonia is unique. So the palynological information supports Takhtajan's view that Paeonia should be elevated to a family (Paeoniaceae) or order (Paeoniales).     

Pseudointegricorpus clarireticulatum (Samoilovitch) Takahashi: morphology and ultrastructure

Dispersed tricolpate pollen of Pseudointegricorpus clarireticulatum (Samoil.) Takah. from the Upper Maastrichtian in Zeya-Bureya Basin, Amur (Heilongjiang) River area, Russian Far East/China has been studied with light and electron microscopy. Pollen size, pole outlines and the shape of equatorial projections show some variation within the species. The exine is striate-reticulate, semitectate and columellate. The species is characterised by highly complex structures that have harmomegathic function and include equatorial projections, endexinous thickenings, difference in the thickness of the infratectum, foot layer and endexine throughout the pollen grain, and equatorial furrows. Exine layers taper towards colpi regions while they break abruptly in furrow regions. The furrows could have helped to shed the exine quickly and enabled pollen germination. A non-extended region with a small cavity in the ectexine was observed in the equatorial region. We think that this region is characteristic of most Triprojectate species.     

Pollen morphology and structure of Tropical and Subtropical American genera of the Piptadenia -group (Leguminosae: Mimosoideae)

A survey of the pollen morphology of the American taxa of the Piptadenia -group (Mimoseae) was done including all together 384 species of the following genera: Piptadenia , Parapiptadenia , Pseudopiptadenia , Piptadeniopsis , Microlobius (= Goldmania ), Stryphnodendron , Adenopodia , Anadenanthera and Mimosa . Because of a high morphological and structural variation the definition and characterization of pollen types turned out to be very difficult. Nevertheless the presence and durability of some pollen characters allow a provisional grouping: (1) always tetrads or polyads, (2) small size 6 (20) 40 mum, (3) unstable shape but currently ovoidal and, if biconvex, ellipsoidal in the outline, (4) number of pollen grains of the polyads very variable and unstable; the most frequent numbers are 8-12-16, (5) pollen grains irregularly united in polyads, with homomorphous exine and, (6) pores always located in the angles of the pollen grains in distal-subdistal position, rarely subdistal, (7) without or with pseudocolpi or subpseudocolpi (never colpi) in the distal face, (8) endexine forming an annulus around the endoaperture with ends of free lamellae with a central white line, (9) the tectal stratum above the pores forming a small vestibular space (except in Anadenanthera ). These palynological characters or most of them confirm the affinity among genera in the Piptadenia -group and its distinction from other taxa of the subfamily Misosoideae with tetrads or polyads.     

Pollen morphology supports the transfer of Wendlandia (Rubiaceae) out of Rondeletieae

Pollen morphology of 27 species, eight subspecies and one variety of Wendlandia was studied using scanning electron microscopy (SEM). Wendlandia pollen are monads, radiosymmetric, small in size, tricolporate (rarely tetracolporate or bicolporate) and spheroidal (rarely subprolate or suboblate) in equatorial view. The compound aperture consists of ectocolpus, mesoporus and endocolpus. In addition, reticulate sexine and granular nexine were observed. The pollen wall ultrastructure of two Wendlandia spp. was examined by transmission electron microscopy (TEM). The exine consists of the tectum, columellae, foot layer and endexine. The endexine is thickened into a costa around the aperture. The intine forms a protruding oncus at the aperture. The palynological characters show a remarkable uniformity among the Wendlandia spp. Differences with Rondeletia, the main genus of tribe Rondeletieae, exist in the exine pattern, the endoaperture and the pollen wall structure. Our observations indicated that the endoaperture type and the structure of the pollen wall of Wendlandia were similar to those of the Gardenieae–Pavetteae–Coffeeae–Octotropideae clade, which provided palynological evidence for a closer relationship of Wendlandia to subfamily Ixoroideae and the transfer of Wendlandia out of Rondeletieae. © 2010 The Linnean Society of London, Botanical Journal of the Linnean Society, 2010, 164 , 128–141.     

Palynological survey of the subtribe Elephantopinae (Asteraceae, Vernonieae)

Despite the taxonomic value of pollen morphology within the tribe Vernonieae, a detailed study of the pollen of the subtribe Elephantopinae is still lacking. The pollen morphology of ten species, representing three of the four genera of the subtribe, Elephantopus, Pseudoelephantopus and Orthopappus, was studied with LM, SEM, and TEM. The pollen of all the species studied was found to be echinolophate, although the differences in aperture features and both sculpture and exine structure allowed recognizing two pollen types. The species of Elephantopus (except for E. elongatus) and Pseudoelephantopus share the regular or more or less regular ridges pattern, the colporate condition but with the ectoapertures little developed, and the acaveate exine structure. From the sculpture and the apertures, the pollen of Caatinganthus harleyi was found to be similar to that of Elephantopus and Pseudoelephantopus. The pollen morphology of the monotypic Orthopappus, which is shared with that of E. elongatus, was further investigated for the first time. We found that it differs from that of the other species in having an irregular pattern of ridges, colporate condition but with a well-developed ectoapertures, and caveate exine. Additional studies of the exine structure and apertures features, coupled with molecular phylogeny, are needed to understand the evolution of pollen characters and re-evaluate the intergeneric relationships within the tribe.     

POLLEN APERTURE EVOLUTION AMONG THE SUBFAMILIES PERSOONIOIDEAE,SPHALMIOIDEAE, AND CARNARVONIOIDEAE (PROTEACEAE)

Pollen apertures were analyzed among the subfamilies Persoonioideae (seven genera; ca. 95 spp.), Sphalmioideae (one genus; one spp.), and Camarvonioideae (one genus; two spp.). Pollen was examined by light microscopy, cryosection, and transmission electron microscopy. Completed studies of pollen apertures among Grevilleoideae (ca. 40 genera; ca. 800 spp.), one of two major subfamilies in Proteaceae, provide a basis for comparison and analysis of aperture evolution among these subfamilies. Aperture characters within Persoonioideae are unique among Proteaceae examined to date. Five distinct aperture types occur among the three subfamilies, three of which (Placospermum, Persoonia, Bellendena) are restricted to Persoonioideae. Sphalmioideae and Camarvonioideae each exhibit a unique aperture organization. The most primitive aperture organization, and one unique to Placospermum, exhibits three main features: 1) a thin, granular endexine continuous around the grain; 2) a heterogeneous foot layer throughout the grain with increased disruptions at the aperture; and 3) only slight differences in exine characters between apertural and nonapertural regions. The Persoonia aperture type represents the next stage of aperture evolution which involves loss of endexine, restriction of a heterogeneous foot layer to the aperture, and marked differences in exine characters between apertural and nonapertural regions. The uniformly homogeneous ektexine in both nonapertural and aperture regions in Bellendena has developed independently. Sphalmium exhibits a primitively thin granular endexine though the restriction of endexine to the aperture is a derived condition. Carnarvonia exhibits several pollen characters also found among Grevilleoideae including: 1) a homogeneous nonapertural ektexine; 2) a slightly heterogeneous apertural ektexine; 3) a lamellate/granulate endexine organized into irregularly shaped “clumps” clustered around the aperture; and 4) a clear demarcation between apertural and nonapertural exine. These characters support the hypothesis that Carnarvonia may have diverged early from the pre-Grevilleoids.     

Pollen morphology in Campanulaceae IV

The exine structure has been studied in Campanulaceae s. lat. The results are combined with those in previous studies of shape, sculpturing and aperture conditions. Fifteen further species have been studied by SEM. Two main groups of pollen are found: (1) porate pollen with spinules and ridges/protrusions or a low relief reticulum, combined with an ektexine varying from simple to complex and a lamellated endexine; (2) 3–colpate/colporate pollen with a high relief reticulate/striate surface sculpturing, in general a homogeneous ektexine and an endexine lacking lamellae. The first group corresponds to Campanulaceae s. str., the second to Lobeliaceae s. str. Some genera like Cyananthus, Codonopsis and Parishella have unique characters which make them difficult to place in any of the two main groups.     

POLLEN MORPHOLOGY AND DETAILED STRUCTURE OF FAMILY COMPOSITAE,TRIBE CICHORIEAE. II. SUBTRIBE MICROSERIDINAE

A survey of pollen morphology of 40 species representing eight genera of the primarily North American subtribe Microseridinae reveals seven of the eight genera to have caveate, echinolophate, tricolporate grains, Picrosia being the only taxon with echinate pollen. Sectioned grains reveal the exine to consist of an ektexine and endexine. The ektexine, composed of spines, columellae, and foot layer appears to be of two basic types, one with six or seven levels of horizontally anastomosing columellae which are reduced to a single columellar layer under the paraporal lacunae and the second, a bistratified ektexine not reduced to a single layer below the paraporal lacunae. Sectioned exines of Pyrrhopappus are unusual, having very large columellae fused to the foot layer below ridges and highly reduced columellae under lacunae. Endexine organization is similar in most of the genera. Exceptions to this are Pyrrhopappus and some species of Agoseris, which have an “endexine 2” layer. Subtribe Microseridinae is essentially stenopalynous. The pollen data support most of the relationships suggested by Stebbins in his classification. The genera Agoseris, Microseris, Nothocalais, and Phalacroseris seem to form a natural group while Krigia and Pyrrhopappus form another cohesive series. The position of Picrosia, as an advanced offshoot of Pyrrhopappus, is not supported by the pollen data.     

Development and cytochemistry of pollen and tapetum in Mitriostigma axillare (Rubiaceae)

The development of pollen grains and tapetum in Mitriostigma axillare (Rubiaceae) was studied from anther primordium to dehiscence. Anthers were freeze-cracked and studied with SEM. Embedded anthers were sectioned and studied with LM and TEM. Cytochemistry was performed in order to distinguish the different layers of the sporoderm and to determine its chemical nature at different development stages. The pollen grains remained as tetrads by partial fusion of the exine, probably because of reduced callose septa during the stage of microspore tetrads within callose envelopes. Characteristic features of the sporoderm were an irregular foot layer, an endexine composed of amalgamated granules, a transient granular-fibrous layer beneath the endexine, and a thin intine. During maturation of the exine, the endexine became chemically different from the ectexine. All layers of the sporoderm were reduced in thickness due to stretching during the engorgement of the pollen grains prior to dehiscence. The pollen grains were colpoidorate with a reticulate to microreticulate tectum covered with a scanty surface coating. The mature pollen grains were binucleate and contained a lot of starch grains. Thick intineous onci protruded through the apertures and formed papillae. About 50% of the microspores were aborted. The tapetum was of secretory type, probably with cycles of hyperactivity and protrusions of the cells into the locular cavity. No syncytium was formed and there were neither orbicules nor tapetal membrane.     

Pollen morphology in relation to pollinators in Papilionoideae (Leguminosae)

The surface sculpturing of the pollen of some species of the taxonomically widely separated genera Harpalyce (tribe Brongniartieae), Camoensia (tribe Sophoreae), Millettia (tribe Tephrosieae), and of the monotypic Dahlstedtia (tribe Tephrosieae) which have large red or white flowers adapted for pollination by birds or bats, is coarsely rugulate or verrucate. Related taxa with small insect pollinated flowers have pollen with simple reticulate or perforate surface sculpturing. The exine stratification of Alexa and Castanospermum (tribe Sophoreae), genera with large red bird-flowers, is complex with a layer of tectal columellae and differs from that of other genera in the tribe Sophoreae which have a normal pollen wall structure. These modifications of pollen structure and sculpture appear to be the result of convergent evolution and a secondary adaptation to pollination. The taxonomic and functional significance of the observations are briefly discussed.     

Pollen morphology of the genera Polygonum s. str. and Polygonella (Polygoneae: Polygonaceae)

The pollen of 30 taxa (27 species, one subspecies and two varieties) in two genera, viz Polygonum s. str. and Polygonella was investigated with LM and SEM, and some selected taxa with TEM. In all genera investigated the pollen is prolate to spheroidal, and the aperture is mostly tricolporate, rarely panto-hexacolporate (especially Polygonum section Polygonum). The exine sculpturing pattern is the most variable feature. Three types of exine can be recognized. Type 1 (Avicularia-Type, sensu Hedberg) - All species of section Polygonum and section Tephis share the smooth tectate exine with spinules, sometimes the surface is more or less rough (Polygonum afromontanum in section Tephis). Type 2 (Pseudomollia-Type, sensu Hong) - Pollen of Polygonum molliaeforme (section Pseudomollia) has the exine, which is verrucose on both poles and nearby the mesocolpium, and mostly psilate around the ectoaperture. Type 3 (Duravia-Type, sensu Hedberg) - Pollen grains of Polygonum section Duravia and Polygonella have the exine which is semitectate-reticulate at the mesocolpium and the poles, and rugulate/reticulate or sometimes foveolate with microspinules around the ectoapertures. The pollen grains in four taxa (viz Polygonum section Pseudomollia, P. section Duravia and genus Polygonella) have a well-marked dimorphism of the ektexine, which is considered to be a synapomorphic condition. The differences of pollen grain between the genus Polygonella and Polygonum section Duravia are almost non existent and clearly interrelated. It is therefore postulated that the similarity in pollen of both taxa is not the result of convergency, but is interpreted as a homology. It is noteworthy that the pollen of Polygonum molliaeforme (section Pseudomollia) appears as intermediate between the Avicularia-type and the Duravia-type, and is well supported the value of separated section for its own. Additionally, in TEM, some exine ultrastructures (e.g. columellae, foot layer, endexine) appear to be valuable characters for comparison between/among taxa. The systematic potentialities of the pollen data of the studied taxa at various systematic levels are also discussed.