The Formation of Pollenkitt in Apium nodiflorum (Apiaceae)

Apium nodiflorum produces a considerable amount of pollenkittwithin a secretory tapetum. ER and plastids (elaioplasts) participatein pollenkitt formation. Both organelles deposit precursorswithin vesicles, which finally fuse to form pollenkitt. Apium nodiflorum L., Apiaceaesecretory tapetum, pollenkitt, ER, plastids, elaioplasts     

Entwicklungsgeschichte und Ultrastruktur des Pollenkitts beiTilia (Tiliaceae)

The pollenkitt ofTilia platyphyllos andT. tomentosa is produced during the tetrade-stage by the tapetum plastides. After tapetum degeneration pollenkitt and accompanying substances are deposited predominantly in the intrabacular spaces of the exine, and only in small quantities on the surface of the exine itself.

     

Ultrastruktur und Verteilung des Pollenkitts in der insekten- und windblütigen GattungAcer (Aceraceae)

Several insect- and wind-pollinated species of the genusAcer have been investigated and compared in regard to pollen stickiness. The considerable amount of very inhomogeneous pollenkitt inA. negundo remains on the loculus wall or is deposited inside the exine cavities; thus the pollen is powdery. The small amount of non-homogeneous, granular pollenkitt inA. campestre mostly disappears into the exine cavities; only small droplets appear on the tectum surface; the pollen stickiness therefore is only moderate. On the other hand,A. pseudoplatanus andA. opalus produce an average amount of granular pollenkitt, which is deposited partially inside the exine and partially as a slender film on the tectum surface; in both the pollen is sticky.A. platanoides contains a great deal of granular and homogeneous pollenkitt; it does not only fill up the exine cavities but also extends as a thick, ± homogeneous, non-granular layer of pollenkitt over the tectum surface; therefore, the pollen is very sticky.—The characteristics of pollen agglutination together with other aspects of floral biology illustrate the wide spectrum between unequivocal entomophily and anemophily within the genusAcer: WhileA. negundo is anemophilous andA. platanoides is entomophilous, the remaining species investigated have a pollination syndrome with entomophilous and anemophilous features and are thus amphiphilous. The evolution withinAcer is tending not only towards dioecy, but also towards anemophily.

Herrn Prof. Dr.L. Geitler zum 80. Geburtstag gewidmet.     

Pollen-wall Proteins: 'Gametophytic' and 'Sporophytic' Fractions in the Pollen Walls of the Malvaceae

Proteins are stored in two sites in the pollen grain walls ofthe Malvaceae, (a) in the cellulosic intine, mainly in the vicinityof the circular apertures, and (b) in cavities in the sculpturedlayer of the exine. The intine-held materials are incorporatedduring the growth of the wall. The exine materials are derivedfrom the tapetum, which during dissolution releases cistemaewith a granular-fibrillar content bounded by ribosomal membranes.This fraction is injected into the exine cavities after thecompletion of wall growth through micropores in the tectum.PAS-reacting material is associated with the injected protein.Another tapetal fraction, lipid in nature and commonly containingcarotenoids, remains on the surface of the pollen grains toform the Pollenkitt. While protein can be detected cytochemically in both intineand exine sites, acid phosphatase and ribonuclease activitywas found to be associated only with the former. Immunofluorescencemethods using antiserum to total pollen leachates showed thatantigens are present in both sites. When the pollen grains are moistened, the exine-held proteinsbegin to pass out through the micro-pores in the tectum within30 s of moistening, while the main discharge from the aperturalintine follows in 4–5 min. These observations, together with evidence from other families,suggest that the intine-held proteins of angiosperm pollen grainsare always produced by the male gametophyte, while those heldin exine cavities are sporophytic in origin, being derived fromthe tapetum. As previously proposed, it seems probable thatin intraspecific incompatibility systems of the gametophytictype control is mediated through intine-held ‘recognitionsubstances’, whereas in sporophytic systems the exine-heldmaterials are concerned.     

Pollenkitt formation in Ilex paraguariensis A.St.Hil. (Aquifoliaceae)

 We investigated the cellular and organelle transformations during the formation of the pollenkitt in the secretory tapetum of Ilex paraguariensis. After the dissolution of the callose surrounding the young microspores, the elaioplasts of the tapetum produce many globules of saturated and unsaturated lipids (plastoglobules). Further on, oleosomes with unsaturated lipids, synthesized in the endoplasmic reticulum, accumulate in the tapetal cytoplasm. In contrast to other species, the plastoglobule production seems to precede the oleosome synthesis. The tapetum shows signs of cellular maturation in the late vacuolated microspore stage, when the plastoglobules and oleosomes coalesce and form the pollenkitt mass. In mature stages of the tapetum the pollenkitt is released into the loculus. Finally, it is mainly deposited on the exine, according to the entomophilous character of this species. The mode of pollenkitt formation in Ilex para guariensis and its transfer to the pollen surface is slightly dissimilar to other Angiosperms. Received October 24, 2002; accepted December 2, 2002 Published online: March 20, 2003     

Developmental stages of the pollen wall and tapetum in some Crocus species

The developmental stages of the pollen wall and tapetum, together with exine morphology were studied in a number of Crocus species, by light and scanning electron microscopy. Gametogenesis was characterized by: 1) development of a thick intine, 2) single mitosis, and 3) terminal amylolysis. The tapetum was of the secretory type. In C. cartwrightianus cv. albus, abnormal sporogenesis and gametogenesis produced vacuolate pollen grains with a reduced-or no intine layer, and rich with starch granules; the tapetum was either of the parietal-or amoeboid type. The exine was echinate and the pollen grains had different types of aperture: furrows, colpi or pores. The ornamentation varied from microreticulate to irregularly perforate. The exine framework was overlaid by a pellicle resistant to chloroform-carbon disulphide, on which a layer of pollenkitt was deposited. The results are discussed from both cytological and evolutionary viewpoints.     

Microsporogenesis in Taxus baccata L.: The Formation of the Tetrad and Development of the Microspores

Following meiosis II in Taxus microsporangia a small proportionof the tetrads regularly degenerated. Despite frequent inequalityin the frequency of ribosomes between the spores of a tetrad,partial degeneration within a tetrad was never observed. Theinitial wall of the young spores was found to resemble the wallof the mother cell in containing a fibrillar layer, and thetwo walls may possess similar isolating properties. The symmetryof the tetrad was regularly iso-bilateral. The formation ofthe sporoderm began as the spores were released into the loculusby the rapid dissolution of the wall of the mother cell. Osmiophilicdroplets emerged from the spore protoplast and entered the wall.The fibrillar layer ceased to be recognizable and the dropletscoalesced to form an outer layer on which up to six sporopolleninlamellae, probably of tapetal origin, were deposited. The accretionof a single layer of sporopollenin droplets, in no recognizablepattern, gave rise to the outer verrucose part of the exine.Cytochemical tests showed that the tapetum was rich in acidphosphatases from the beginning of meiosis. Towards the endof its degeneration the tapetum intruded into the loculus andcould therefore be regarded as partly invasive. Taxus baccata, microsporogenesis, tetrad symmetry, sporoderm     

Pollen Ontogeny in Catananche caerulea L. (Compositae: Lactuceae) II. Free Microspore Stage to the Formation of the Male Germ Unit

The development of Catananche caerulea pollen grains from theearly free microspore stage to the formation of the male germunit has been studied using the scanning electron microscope.The differentiation of the elaborate ectexine from primexineand the accompanying cytoplasmic changes in the microsporesare described. Changes in the tapetum, reflecting first theformation of sporopollenin precursors and then of pollenkitt,are also described. The origin of taxonomically important featuresis discussed. Catananche caerulea, Compositae: Lactuceae, microspore mitosis, male germ unit, ontogeny, primexine differentiation, scanning electron microscopy     

Entwicklungsgeschichte und Ultrastruktur von Pollenkitt und Exine bei nahe verwandten entomophilen und anemophilen Angiospermensippen derAlismataceae,Liliaceae, Juncaceae,Cyperaceae, Poaceae undAraceae

Some closely related members of the monocotyledonous familiesAlismataceae, Liliaceae, Juncaceae, Cyperaceae, Poaceae andAraceae with variable modes of pollination (insect- and wind-pollination) were studied in relation to the ultrastructure of pollenkitt and exine (amount, consistency and distribution of pollenkitt on the surface of pollen grains). The character syndromes of pollen cementing in entomophilous, anemophilous and intermediate (ambophilous or amphiphilous) monocotyledons are the same in principal as in dicotyledons. Comparing present with former results one can summarize: 1) The pollenkitt is always produced in the same manner by the anther tapetum in all angiosperm sub-classes. 2) The variable stickiness of entomophilous and anemophilous pollen always depends on the particular distribution and consistency of the pollenkitt, but not its amount on the pollen surface. 3) The mostly dry and powdery pollen of anemophilous plants always contains a variable amount of inactive pollenkitt in its exine cavities. 4) A step-by step change of the pollen cementing syndrome can be observed from entomophily towards anemophily. 5) From the omnipresence of pollenkitt in all wind-pollinated angiosperms studied one can conclude that the ancestors of anemophilous angiosperms probably have been zoophilous (i.e. entomophilous) throughout.

     

Pollenkitt is lacking inGnetum gnemon (Gnetaceae)

The anther tapetum of the gymnospermGnetum gnemon produces no lipid osmiophilous droplets as pollenkitt forerunners. Thus—in contrast to entomophilous and anemophilous angiosperms—no pollenkitt is produced at all. From lack of pollenkitt in other gymnosperms, it appears to be restricted to angiosperms. This can be considered as new and additional proof for the hypothesis that the angiosperms are one coherent phylogenetic group, and that the development of pollenkitt in their ancestors was one of the main prerequisites for the adaptive switch to entomophily.     

Pollen Wall Development in Gibasis (Commelinaceae)

The development of the one and-inline of the pollen wall aredescribed for Gibasis karwinsk yana and G. venustula. Duringthe tetrad stage the appearance of electron-opaque depositionsor tri-partite plates at discrete sites between the plasma membraneof the spore and the inward surface of the callose special wallare the first indications of exine development. The sulcus rapidlydifferentiates being composed of discrete exine granules ona thin foot layer. Probacula in non-apertural areas developin an electron-opaque granular layer situated between the plasmamembrane, which is highly convoluted, and the callose specialwall. A foot layer is formed from electron-opaque lamellae atthe plasma membrane. Exine pattern is clearly established withinthe tetrad. After release of the spores from the tetrad an intimate associationis rapidly developed between the plasma membrane of the periplasmodialtapetum and the newly-formed exine. Compacted electron-opaquematerial is found at the interface between membrane and theexine and vesicular material is added from the tapetum. Theincrease in volume that occurs in both spore and anther is accompaniedby considerable vacuolation. Intine development begins just prior to pollen grain mitosisand continues rapidly at the aperture. The thin foot layer becomesdiscontinuous. Further intine deposition takes place after mitosisand a bilayer is apparent in mature grains. The matrix of thislayer contains conspicuous electron-opaque platelets. The exineof the mature spore stains less intensely than in the youngspore and the interbacula spaces are filled with material fromthe degenerate tapetum. Gibasis karwinskyana, Gibasis venustula, Commelinaceae, exine, intine, tapetum, pollen wall, ultrastructure     

A Comparison of Anther Tissue Development in Male Sterile Aloe vera and Male Fertile Aloe ciliaris

Cytological differences between the anther development of amale sterile and a male fertile Aloe species are used to explaininteractions between anther tissues. Some deviations in thelayers of the locule wall and the microspores of the male sterileanther are related to each other and their biological functionsare discussed. The cytological development of the male sterility,which can be observed shortly after meiosis, seems to be restrictedto the locular cavity. The tapetal development and breakdownare normal, apart from the size of some orbicules. However,the pollenkitt is not transported to the pollengrains, whichstrongly supports our theory that this process is mechanicallypollen-controlled. The development of the epidermal and endothecialcells is normal, except in a part of the anthers where thesecells do not expand, after which dehiscence is incomplete. Thelatter process is discussed in relation to the deviations insidethe locular cavity. Aloe vera (L.) Burm. fil., Aloe ciliaris Haw., Liliaceae, male sterility, tapetum, pollenkitt, endothecium, anther dehiscence     

On the Origin,Development and Ultrastructure of the Orbicuies and Pollenkitt in the Tapetum of Anemarrhena Asphodeloides (Liliaceae)

Anemarrhena asphodeloides Bunge is a monotypic genus of Liliaceae, growing in China and Korea. The pro‐orbicules are derived from the cisternae of rough endoplasmic reticulum. There are prominent aggregates of orbicuies in Anemarrhena. The first sign of the formation of pollenkitt is that the proplastids begin to differentiate into elaioplasts in the tapetum, and then the elaioplasts become the main source of pollenkitt. Alternatively, cytoplasmic vesicles derived from RER are probably the other way pollenkitt is synthesed in this species.     

Anther, pollen and tapetum development in safflower, Carthamus tinctorius L

In safflower, the anther wall at maturity consists of a single epidermis, an endothecium, a middle layer and the tapetum. The tapetum consists mainly of a single layer of cells. However, this single-layer appearance is punctuated by loci having ‘two-celled’ groupings due to additional periclinal divisions in some tapetal cells. Meiotic division in microsporocytes gives rise to tetrads of microspores. The primexine is formed around the protoplasts of microspores while they are still enveloped within the callose wall. Just prior to microgametogenesis, the microspores enlarge through the process of vacuolation, and the exine wall pattern becomes established. Microgametogenesis results in the formation of 3-celled pollen grains. The two elongated sperm cells appear to be connected. The exine wall is highly sculptured with a distinct tectum, columellae, a foot layer, an endexine and a thin intine. Similar to other members of the Asteraceae family, the tapetum is of the invasive type. The most novel finding of this study is that in addition to the presence of invasive tapetal cells, a small population of ‘non-invasive’ tapetal cells is also present. The tapetal cells next to the anther locules in direct contact with the microspores become invasive and start to grow into the space between developing microspores. These tapetal cells synthesize tryphine and eventually degenerate at the time of gametogenesis releasing their content into the anther locules. A smaller population of non-invasive tapetal cells is formed as a result of periclinal divisions at the time of tapetum differentiation. These cells are not exposed to the anther locules until the degeneration of the invasive tapetal cells. The non-invasive tapetal cells have a different cell fate as they synthesize pollenkitt. This material is responsible for allowing some pollen grains to adhere to each other and to the anther wall after anther dehiscence. This observation explains the out-crossing ability of Carthamus species and varieties in nature.     

“Pollen Buds” in Ophiorrhiza (Rubiaceae) and their Role in Pollenkitt Release

Pollen buds are apertural protrusions formed by the ectintine. In their wall unesterified and methyl-esterified pectins are detected by immunogold labeling. During pollenkitt formation pollen buds become adpressed and connected to the tapetum wall. The following expansion of the endothecium causes the mechanical rupture of the tapetum at the binding sites of the pollen buds. These events are accompanied by the release of the pollenkitt.     

Entwicklungsgeschichte und Ultrastruktur von Pollenkitt und Exine bei nahe verwandten entomophilen und anemophilen Angiospermensippen:Ranunculaceae,Hamamelidaceae, Platanaceae undFagaceae

Transfer of fresh pollen either by wind or by insects is strongly related to the degree of its stickiness. The sticky substances involved should be understood as pollenkitt. Ultrastructural investigations indicate that the sticky pollen of entomophilous angiosperms (in this publicationHamamelis vernalis andH. virginiana, Corylopsis platypetala) results from the deposition of usually electron-dense, homogeneous pollenkitt mainly on the outside layer of the exine. In contrast, the pollen of anemophilous angiosperms (in this publicationParrotia persica, Platanus orientalis, Thalictrum flavum andQuercus robur), but also of some entomophilous angiosperms with special pollination ecology (e.g.Aquilegia vulgaris) is rather dry and powdery. In these cases the pollenkitt often is electron-transparent and inhomogeneous and is mainly removed into the cavities of the exine. Ultrastructure and deposition of pollen and pollenkitt in ambophilous angiosperms (in this publicationThalictrum minus, Castanea sativa) are ± intermediate.

     

The tapetum: Its form,function, and possible phylogeny inEmbryophyta

It appears that the tapetum is universally present in land plants, even though it is sometimes difficult to recognize, because it serves mostly as a tissue for meiocyte/spore nutrition. In addition to this main function, the tapetum has other functions, namely the production of the locular fluid, the production and release of callase, the conveying of P.A.S. positive material towards the loculus, the formation of exine precursors, viscin threads and orbicules (= Ubisch bodies), the production of sporophytic proteins and enzymes, and of pollenkitt/tryphine. Not all these functions are present in all land plants:Embryophyta. Two main tapetal types are usually distinguished in theSpermatophyta: the secretory or parietal type and the amoeboid or periplasmodial type; in lower groups, however, other types may be recognized, with greater or lesser differences. A hypothetical phylogenesis of the tapetum is proposed on the basis of its morphological appearance and of the nutritional relations with meiocytes/spores. The evolutionary trends of the tapeta tend towards a more and more intimate and increasingly greater contact with the spores/pollen grains. Three evolutionary trends can be recognized: 1) an intrusion of the tapetal cells between the spores, 2) a loss of tapetal cell walls, and 3) increasing nutrition through direct contact in narrow anthers.     

Tapetal Cell Changes and Sporoderm Development in Rhigozum trichotomum (Burch.)

Rhigozum trichotomum is a perrenial woody shrub which is indigenousto the arid regions of southern Africa. Primexine developmentis initiated while the microspores are still enclosed by callose.This is followed by the appearance of probacula which give riseto the tectum, bacula and nexine. At the time of callose dissolution,the exine pattern is well established and intine developmenthas been initiated. During the tetrad stage, the protoplastsof the tapetal cells exhibit shrinkage while conspicuous stacksof rough endoplasmic reticulum become evident in their cytoplasm.These stacks produce numerous vesicles which are associatedwith lipid globules and which migrate to the tapetal/locularwall where, it is suggested, they give rise to the pro-orbicules.The pro-orbicules become coated with an osmiophilic substance,probably sporopollenin, and are released into the thecal fluidto become intimately bound to the exine, Here they are strippedof the osmiophilic layers which appear to be incorporated intothe sporoderm. Rhigozum trichotomum (Burch.), sporoderm, pollen wall, exine, orbicules, pro-orbicules, sporopollenin, tapetum     

Response of CO2 uptake, chlorophyll content, and some productional features of forest herb Smyrnium perfoliatum L. (Apiaceae) to different light conditions

Smyrnium perfoliatum L. (Apiaceae), an endangered summer forest herb grown in the understory of dominant oak-hornbeam stands in Devinska Kobyla, Little Carpathians region in SW Slovakia, is considered to form at least five leaf types of different physiological and anatomical quality. These observation are based upon the estimated differences of photosynthetic carbon dioxide uptake, chlorophyll content, leaf anatomy, and several quantitative parameters of growth analysis. There is a further attempt to establish, to what extent the daily changing environment, especially the excess of light of fast-moving sun-flecks by the photosynthetic apparatus within any leaf type, according to its dominant shade adaptation could be effectively used.