Studies on the Pollen Morphology and Seed Coat of the Genus Cistanche (Orobanchaceae) in China

In the present paper pollen grains of 5 species and seed coat of 4 species of the genus Cistanche (Orobanchaceae) from China were examined by scanning electron microscope As a result, two types of the pollen exine sculpture are distinguished: (1) tuberculate, C. salsa and C. lanzhouensis; (2) rugulate or fine reticulation formed by the fusion of rugae, C. sinensis, C. deserticola and C. tubulosa. Chinese Cistanche was classified into two sections based on the gross morphology by the present author (Zhang, 1984). C. lanzhouensis and C. sinensis were included in one section. This classification is in conflict with the pollen type, which indicates that the characters of pollen grains and external morphology in this genus have evolved at different rates. The differences in pollen morphology of Chinese Cistanche can serve as characters for delimitating species. According to our abservation, C. lanzhouenis Z. Y. Zhang differs from the other members of Cistanche not only in external morphology but also in pollen morphology. Pollen grains are subprolate in this species, while prolate in the other four species, and exine sculpture is tuberculate. The present study provides the establishment of this new species (Zhang, 1984) with palynological evidence. The seed coat sculpture in Chinese Cistanche are constantly alveolate, but there are some slight differences, by which the sculpture can be divided into two types: (1) testa cells have or have not thickenings on the inner anticlinal walls; cavernulous sculpture is present on outer periclinal wall of some cells: C. sinensis; (2) testa cells have striate thickenings on the inner anticlinal walls: C. salsa, C. deserticola and C. tubulosa. The characters of seed coatof some significance for the delimitation of species.     

Presence of the protruding oncus is affected by anther dehiscence and acetolysis technique

A protruding oncus is a projection of the intine in the aperture region. The ubiquitous use of acetolysis in palynological research has led to the presence of a protruding oncus being underreported. Controlled experiments with pollen samples collected from undehisced and dehisced anthers demonstrate that the presence of a protruding oncus is affected by the state of the anther at maturity: dehisced or undehisced and by the preparation technique. In investigating the occurrence of onci, particular attention should be paid both to the dehiscence state of the anthers and the effect of the preparation technique on the intine. Although it has been suggested that protruding onci and pollen buds can be distinguished based on three criteria (size, presence of a large vacuole, separation of the protrusion from the grain), most of these distinctions break down when information is included from more recent studies. Additional study of protruding intinous structures may help clarifing the difference between pollen buds and protruding onci.     

Anther structure and pollen development in Melicoccus lepidopetalus (Sapindaceae): An evolutionary approach to dioecy in the family

Anther and pollen development in staminate and pistillate flowers of dioecious Melicoccus lepidopetalus (Sapindaceae) were examined by light and electron microscopy. Young anthers are similar in both types of flowers; they consist of epidermis, endothecium, two to four middle layers and a secretory tapetum. The microspore tetrads are tetrahedral. The mature anther in staminate flowers presents compressed epidermal cells and endothecium cells with fibrillar thickenings. A single locule is formed in the theca by dissolution of the septum and pollen grains are shed at two-celled stage. The mature anthers of pistillate flowers differ anatomically from those of staminate flowers. The epidermis is not compressed, the endothecium does not develop fibrillar thickenings, middle layers and tapetum are generally persisting, and the stomium is nonfunctional. Microspore degeneration begins after meiosis of microspore mother cells. At anthesis, uninucleate microspores and pollen grains with vegetative and generative nuclei with no cytokinesis are observed. Some pollen walls display an abnormal exine deposition, whereas others show a well formed exine, although both are devoid of intine. These results suggest that in the evolution towards unisexuality, the developmental differences of anther wall tissues and pollen grains between pistillate and staminate flowers might become more pronounced in a derived condition, such as dioecy.     

The Apertural Wall in Pollen of Linum grandiflorum

The apertural wall in tricolpate pollen of Linum grandiflorumwas investigated in order to understand its functioning duringdesiccation and rchydration. Whole and sectioned pollen grainswere studied with light or electron microscopy and by cytochemicalmeans. The areas of the apertures were examined in fresh drypollen, in grains moistened on agar gel or removed from compatiblestigmas, and in pollen from mature undehisced anthers The intine was found to consist of an inner ß-glucanlayer and an outer pectic layer. At the apertures the pecticlayer is thickened and overlaid by a ß-glucan layer.The pectinaceous intine stains red with basic fuchsin. The presenceof a third wall layer, the medine, was not confirmed. The aperturalintine thickenings possess considerable imbibitional capacityand at rehydration they appear as swollen lenticular bodies A procedure is described for obtaining intact exine free grains(EFG's) and whole, separated exines of L. grandiflorum. Invariably,the released EFG's consisted of protoplasts encased in the cellulosicintine. In most grains the outer intine remained attached tothe separated exine In L. grandiflorum the outer wall of the aperture expands whilethe protoplast and endintine are still infolded. Apparently,the exintine becomes detached from the endintine during desiccationand re-attaches at rehydration. It is suggested that the transientdetachment controls the influx of water into the vegetativecell Except for morph-specific exine processes no differences instructure of the aperture wall or its functioning at rehydrationwere observed between pin and thrum grains Pollen wallM, apertures, exintine, exine free grains, rehydration, desiccation, Linum grandiflorum     

Localization of ubiquitin in anthers and pistils of Nicotiana

Ubiquitin-conjugated compounds were localized in anthers and pistils of Nicotiana alata by immuno-cytochemistry. In young anthers, antibodies to ubiquitin bound to callose cell walls surrounding pollen mother cells and to organelles in the endothecium. At the freespore stage, antibodies bound to circular-cell cluster cells subtending the stomium and to organelles and cell walls of endothecial cells. Near anther dehiscence, locular material was labeled. In pistils, cell walls of stylar transmitting tissue were labeled in a beaded pattern. Antibodies bound to a thin layer surrounding ovules, to the lining of embryo sacs, to cytoplasm of eggs and synergids, and to starch grains in central cells. Sites of localization were tissue- and time-specific, suggesting a regulatory role for ubiquitin in development of reproductive structures in flowering plants.     

Pectin distribution pattern in the apertural intine of Euphorbia peplus L. (Euphorbiaceae) pollen

The apertural inner layer (intine) of Euphorbia L. pollen grains has a characteristic but original structure that has paired thickenings, one on either side of the colpus. To determine the nature and role of this intine layer, pollen grains of Euphorbia peplus L. were germinated in vivo and in vitro. The germination process involves wall changes that facilitate formation of the pollen tube and its subsequent growth. In the thickenings of the intine of E. peplus, the unesterified pectin epitopes are more densely localised in the inner part of the middle intine. No such epitopes are located in the intine portion adjacent to the plasma membrane (cellulosic endintine). Unesterified pectin epitopes are also localised in the outer part of the intine but are restricted to the centre of the aperture, around and in the pore. The de-esterification of pectins is very advanced at the time of dehiscence and pollen germination. The stratification of the aperture intine may take the following pathway at the time of germination: the thin outer zone of the intine in the pore region becomes disorganised and undergoes dissolution with liberation of unesterified and esterified pectins; the middle intine thickenings undergo an important elastic modification, but without liberation of unesterified pectins; the cellulosic inner intine is the progenitor of the pollen tube wall. This special intine of E. peplus is an adaptation to the hydration process preceding germination, increasing intine and pollen grain wall elasticity.     

Calcium distribution in fertile and sterile anthers of a photoperiod-sensitive genic male-sterile rice

Potassium antimonate was used to locate Ca²⁺ in fertile and sterile anthers of a photoperiod-sensitive genic male-sterile rice (Oryza sativa L. japonica). During the development of fertile anthers, abundant calcium precipitates accumulated in the anther walls and on the surface of pollen grains and Ubish bodies at the late developmental stage of the microspore, but not in the cytoplasm of pollen grains. Following the accumulation of starch grains in pollen, calcium precipitates on pollen walls diminished and increased in parenchymatous cells of the connective tissue. In sterile anthers, calcium precipitates were abundant in the middle layer and endothecium, but not in the tapetum, as was found in fertile anthers. A special cell wall was observed between the tapetum and middle layer of sterile anthers that appeared to relate to distinctive calcium accumulation patterns and poor pollen wall formation in the loculi. The formation of different patterns of antimonate-induced calcium precipitates in the anthers of photoperiod-sensitive genic male-sterile rice indicates that anomalies in the distribution of calcium accumulation correlate with the failure of pollen development and pollen abortion. Received: 30 May 1997 / Accepted: 5 July 1997     

Differential Staining of Aborted and Nonaborted Pollen

A single staining solution was made by compounding it in the following order (dyes were from British Drug Houses): ethanol, 10 ml; 1% malachite green in 95% ethanol, 1 ml; distilled water, 50 ml; glycerol 25 ml; phenol, 5 gm; chloral hydrate, 5 gm; acid fuchsin 1% in water, 5 ml; orange G, 1% in water 0.5 ml; and glacial acetic acid, 1-4 ml. For best results in differentiation to give green pollen walls and red protoplasm, the staining solution should be acidified with glacial acetic acid. The amount of acid to be added depends upon thickness of the pollen walls: for very thin-walled pollen, 1 ml; for moderately thin walls, 2 ml; and for thick-walled or spiny-walled pollen, 3 ml of acid. For pollen inside non-dehiscent anthers, 4 ml of acid should be used. Staining is hastened by flaming the slide (for loose thin-walled pollen) or by immersing thick-walled pollen or anthers for 24-48 hr at 50 C. In the typical stain, aborted pollen grains are green; nonaborted, red. The method is useful for pollen inside nondehiscent anthers if these are small and not too deeply coloured naturally. The stain is very durable, especially if the coverslips are sealed with param wax. The staining solution will keep well for about a month. It is useful both for angiosperms and gymnosperm microgametes.     

Microsporogenesis of the feathers (fertile branches derived from annual buds) in Vitis vinifera,cv Picolit giallo

Abstract

Using light and electron microscopy, we have studied the microsporogenesis and tapetal development of the feathers in two different low producing clones of Picolit giallo (sp. Vitis vinifera). In these clones while the productivity of the main branches (fertile branches originated from buds, formed in the previous year, that remained silent during the winter) is very low, that of the feathers (fertile branches derived from annual buds) is always normal.

The microsporogenesis and tapetal development proceed normally in almost all the examined anthers; it is remarkable that at the tetrad stage the tapetal cells appear well structured without any degeneration symptom, unlike what observed for the main branches. Moreover in most of the mature anthers the pollen grains are numerous, pleinty of organelles and show sometimes thickenings in the callose layer under their wall. The tapetal cells of these anthers have disappeared. Only in few anthers we observed the presence of collapsed pollen grains and tapetal cells with anomalous development, that are still present when the pollen grains are mature. This rare situation for the feathers is on the contrary frequent for the main branches.     

Anther development, microsporogenesis and microgametogenesis in Heliconia (Heliconiaceae, Zingiberales)

Anther development, microsporogenesis and microgametogenesis in several species of Heliconia were investigated as part of a complementary embryological study of the Heliconiaceae. All studied Heliconia species present bithecate and tetrasporangiate anthers with fertile pollen grains; only H. rivularis, a natural hybrid, presented sterile pollen grains of variable size and no content. The anther wall has an uniseriate epidermis and endothecium, the latter with helicoidal thickenings, although some cells of the middle layers also showed thickenings; the biseriate tapetum is of amoeboid non-syncytial type, since the tapetum cells did not fuse together forming a true plasmodium. The microsporogenesis is successive leading to isobilateral tetrads. The inaperturate pollen grains had a very reduced exine consisting of a thin, more or less continuous layer with small spines upon; the pollen grain shape is variable among the species, all of them presenting heteropolar pollen, except H. angusta with isopolar ones. Most of these characteristics were shared with other studied Zingiberales, although more studies need to be done.     

PATTERNS OF ENDOTHECIAL WALL THICKENINGS IN ARACEAE: SUBFAMILIES POTHOIDEAE AND MONSTEROIDEAE

A survey of the patterns of endothecial wall thickenings in 106 representative species from 20 genera in the Pothoideae and Monsteroideae was made using cleared anthers, sections and macerations. The wide variety of wall thickenings that is present is based on an annular-helical pattern. Variations in thickenings are related to differences in cell shape, cell orientation, intergradation between helical and annular patterns, pitch of helices, presence of branched thickenings, and various types of discontinuities in thickenings. Notable exceptions to the annular-helical pattern include Culcasia, which lacks a differentiated endothecial layer with thickenings, and Acorus, which has a peculiar stellate pattern that is unique in the family. No single pattern consistently characterizes either subfamily, although continuous helices are common in the Monsteroideae, and rare in the endothecium of Pothoideae (except Anadendrum). Monsteroideae frequently exhibit a series of slanted separate thickenings on anticlinal walls, which is absent from Pothoideae except in Heteropsis. The slanted pattern is considered a variation on a rectangular helix, involving discontinuities of thickenings on the periclinal walls. Some monsteroid genera show considerably more interspecific variation (Rhaphidophora) than others (Monstera). Endothecial thickenings constitute an anatomical character that is useful in the systematic study of Araceae; present results support other anatomical studies in identifying Culcasia and Acorus as highly divergent genera in the Pothoideae.     

SEM COMPARISON OF FRUITS OF A SEAGRASS,HALODULE (CYMODOCEACEAE), FROM AUSTRALIA AND TEXAS

Fruits of Halodule were collected from marine sediments in Shark Bay, Western Australia, and in Laguna Madre, Texas, and compared using scanning electron microscopy. The fruits of the Australian collection had a more deeply furrowed wall surface, and the fruits of the Texas collection had a more prominent stylar beak. The fruits of both collections had walls that were composed of irregularly interlocking cells, each with multilayered, concentric cell walls. The fruit wall separates into nearly equal halves along a cleavage line composed of cells that are not interlocked. The seed coats are composed of flattened cells with annular thickenings and the oblong hypocotyls are composed of large, polygonal cells that contain starch grains. The cotyledon and plumule are folded into a hypocotylary invagination along the line of wall separation. A radicle hump or short radicle develops during germination in seawater. Although the taxonomy of Halodule has been based on a vegetative feature, the leaf tips, fruit differences may be of diagnostic value.     

Seed Epidermis Development and Histochemistry in Solanum melongena L. and S. violaceum Ort.

Structure, development and histochemistry of the seed epidermiswere studied inSolanum melongena L. andS. violaceum Ort. usinglight and scanning electron microscopy. The epidermal cellsat the endosperm mother cell stage of ovule development hadthickened outer periclinal walls, consisting of two layers,a thin inner layer, and a thick outer layer. The latter whichstained positively for pectic substances became further thickenedduring the course of seed development; more so inS. melongena.The inner layer of the outer periclinal wall also was thickenedby depositions of cellulose but remained comparatively thin.The development of the inner periclinal and anticlinal wallstook place by the uneven deposition of concentric layers. Thesesecondary wall thickenings which appeared as pyramids in transversesection stained for cellulose, lignin and pectin. Further unevensecondary thickenings near the outer part of the anticlinalwalls resulted in the formation of projections which were hair-or ribbon-like in appearance. InS. melongena, these projectionsprogressed only a short distance from the anticlinal wall. InS.violaceum, on the other hand, they grew much longer formingstriations on the inside of the outer periclinal wall. InS.melongena, partial removal of the outer periclinal wall by enzymeetching exposed to surface view a beaded appearance of the cellboundaries. Complete erosion of the outer periclinal wall revealedthe hair-like projections of the underlying anticlinal walls.InS. violaceum, enzyme treatment exposed the striations whichformed bridge-like structures over the curves in the anticlinalwalls. Solanum melongena ; Solanum violaceum; seed epidermis; seed structure; seed development; cell wall histochemistry; cell wall projections; cell wall striations     

FLORAL MORPHOLOGY AND CROSS-POLLINATION IN ERYTHRONIUM GRANDIFLORUM (LILIACEAE)

In bumblebee visits to flowers of Erythronium grandiflorum (Liliaceae), the ratio of self- to nonself- (“outcross”) pollen grains deposited on the stigma is positively correlated with the degree of stylar exsertion beyond the anthers. Natural populations show substantial, continuous variation in stylar exsertion.     

Lily (<Emphasis Type="Italic">Lilium longiflorum</Emphasis> L.) pollen protoplast adhesion is increased in the presence of the peptide SCA

The style of lily produces a specialized extracellular matrix (ECM) in the transmitting tract epidermis that functions to guide pollen tubes to the ovary. This adhesive ECM contains low esterified pectins and a peptide, SCA (stigma/stylar cysteine-rich adhesin). Together they form a matrix to which pollen tubes adhere as they grow through the style. Pollen tubes also adhere to each other but only when grown in vivo, not in vitro. Pollen does not produce detectable SCA, but when SCA is added to an in vitro growth medium, it binds to pollen tubes that have esterified and low-esterified pectins in their walls. Since adhesion of the pollen tube to the stylar matrix requires tip growth, we hypothesized that the pectin wall at the pollen tube tip interacted with the SCA protein to initiate adhesion with the stylar pectin [Lord (2000) Trends Plant Sci 5:368–373]. Here, we use a pollen protoplast system to examine the effect of SCA on protoplast adhesion when it is added to the growth medium in the absence of the stylar pectin. We found that SCA induces a 2-fold increase in protoplast adhesion when it is added at the start of protoplast culture. This effect is less when SCA is added to the medium after the cell wall on the protoplast has begun to regenerate. We show that among the first components deposited in the new wall are arabinogalactan proteins (AGPs) and highly esterified pectins. We see no labeling for low esterified pectins even after 3 days of culture. In the pollen protoplast culture, adhesion occurs in the absence of the low esterified pectin. The newly formed wall on the protoplast mirrors that of the pollen tube tip in lily, which is rich in AGPs and highly esterified pectins. Thus, the protoplast system may be useful for isolating the pollen partner for SCA in this adhesion event.     

Pollen dimorphism and anther culture in barley

Summary A dimorphism is observed in barley (Hordeum vulgare L., cv. Akka) pollen when stained with acetocarmine from the mid-binucleate stage onwards. The majority of grains have staining cytoplasms, while the remainder have cytoplasms which take up little or no stain (NS grains). The staining dimorphism cannot be detected at the late-uninucleate microspore stage when anthers are normally cultured, but the evidence suggests that the microspores have already diverged at this time and it is the cells destined to become NS grains in vivo that respond in culture to become pollen calluses. Evidence comes from a comparison of the frequencies of NS grains and pollen calluses and from their distribution between and within anthers.     

希茉莉（Hamelia patens Jacq.）花粉发育时期快速检测

茜草科希茉莉（Hamelia patens Jacq.）的花粉用DAPI（4’,6-diamidino-2-phenylindole）直接染色不能观察到花粉核,本研究探索出适宜在DAPI染色前处理希茉莉花粉壁的水浴加热-氧化方法,使得希茉莉花粉核能在荧光显微镜下清晰地显示出来,从而快速检测花粉所处的发育阶段。结果表明：（1）单核花粉和二核花粉最适宜的水浴加热温度和时间分别为65℃、20~50 min和55℃、20~40 min;（2）花粉发育阶段与花朵、花药长度的对应关系为：花朵0.90~1.00 cm、花药0.50~0.60 cm时对应花粉的四分体时期,花朵1.10~1.60 cm、花药0.60~0.85 cm时对应单核花粉时期,花朵1.80~2.70 cm（花冠裂片张开前）、花药0.91~1.01 cm时对应二核花粉时期。     

Aperture Orientation in Laurelia Pollen (Atherospermataceae Syn. Subfamily Atherospermoideae of Monimiaceae)

The development of the encircling aperture of pollen grains or the New Zealand species Laurelia novae-zelandiae is described by means of light and scanning electron microscopy. Some observations are also reported from pollen development and structure in the South American species Laurelia sempervirens, mature pollen of which can be distinguished from that of L. novae-zelandiae. The aperture begins to develop while pollen of L. novaezelandiae is still in tetrads, and passes through the distal and proximal poles of each grain. The widest parts of the mature aperture are at and near what are morphologically the distal and proximal poles of each grain. No such meridionosulcate type of pollen was recorded in a recent survey of pollen aperture types of primitive angiosperms and contradicts a recent report that pollen in the Atherospermataceae had equatorially aligned apertures.     

Investigation on the Ontogeny of Pollen in Pinus thunbergii Parl

The microsporogenesis in Pinus thunbergii occurs in early to middle March, and the development of pollen in late March to early April. A mature pollen grain consists of four cells. The starch grains aggregate in the equators during meiosis Ⅰ to Ⅱ. The callose materials appear first in inner side of the wall of meiocyte and then in the equator. Sometimes the 3-or 4-sac- cate pollen grains have been found. In the ontogeny of pollen in Pinus thunbergii following events are noteworthy. (1) During meiosis the equatorial aggregation of starch grains in me iocyte becomes conspicuous. (2) During formation of tetrad the callose wall appears in regular activity. It is noteworthy that there is itself feature for the accumulation of callose in Pinus thunbergii. After formation of prothallial cells the callose appears mainly in the area between body and saccus. So the prominent symmetry of distribution of callose occurs in the pollen grains. But almost no callose accumulation takes place i,n tenuity in distal face of pollen grain. On the contrary, there are certain callose accumulation around the prothallial cells in the proximal face, forming the polar distribution of callose in pollen grains.