Megasporogenesis,Microsporogenesis and Development of Gametophytes in Eleutherococcus senticosus (Araliaceae)

This paper describes megasporogenesis, microsporogenesis, and development of female and male gametophytes in Eleutherococcus senticosus. The main results are as follows: Flowers of E. senticosus are epigynous, pentamerous. Anthers are 4 -microsporangiate. An ovary has 5 loculi. Each ovary loculus has 2 ovules: the upper ovule and the lower ovule. The upper one is orthotropous and degenerates after the formation of archesporial cell, while the lower one is anatropous, unitegmic and crassinucellar, and able to continue developing. In male plants, microsporogenesis and development of male gametophytes took place in regular way, but a series of abnormal phenomena were found in megasporogenesis and development of female gametophytes. The microspore mother cells gave rise to tetrahedral tetrads by meiosis. Cytokinesis was of the simultaneous type. The mature pollen was 3-celled and shed singly. The anther wall formation belonged to the dicotyledonous type. At the stage of microspore mother cell, the anther wall consisted of four layers, i.e. epidermis, endothecium, middle layer, and tapetum. The tapetum was of glandular type and its most cells were binucleate. When microspores were at the uninucleate stage, the tapetum began to degenerate in situ. When microspores developed into 3-celled pollen grains, the tapetum had fully degenerates. In the lower ovule of male flower, the megaspore mother cell gave rise to a linear or “T” -shaped tetrad. In some cases, a new archesporial cell over the tetrad or two tetrads parallel or in a series were observed. Furthermore, the position of functional megaspore was variable; any one or two megaspores might be functional, or one megaspore gave rise to a uninucleate embryo sac, but two other megaspores also had a potentiality of developing into the embryo sac. In generally, on the day when flowers opened, female gametophytes contained only 4 cells: a central cell, two irregular synergids and one unusual egg cell. In female plants, microspore mother cells and secondary sporogenous cells were observed. But at the stage of secondary sporogenous cell, the newly differentiated tapetum took the appearance of degeneration. Later, during the whole stage of meiosis, the trace of degenerative tapetum could be seen. At last, the microsporangium degenerated and no tetrad formed. On the blossom day, all anthers shriveled without pollen grains. In female flowers, megasporogenesis and development of female gametophytes were normal: the tetrad of megaspores was linear or “T”-shaped; the chalazal megaspore was usually functional; the development of embryo sac was of the Polygonum type. On the blossom day, most embryo sacs consisted of 7 cells with 8 nuclei or 7 cells with 7 nuclei; but the egg apparatus was not fully developed. In hermaphroditic plants, microsporogenesis was normal but the development of male gametophytes was partially abnormal. When the hermaphroditic flowers blossomed, there were more or less empty pollen grains in the microsporangium and these pollen grains were quite different in size. The development of most gynoecia was normal but numerous abnormal embryo sacs could be seen. On the blossom day, female gametophytes were mainly 7-celled with 8-nuclei or with 7-nuclei or 4-celled with antipodal cells degenerated; the egg apparatus wasnot fully developed either.     

短柄五加开花后雌蕊的发育状态与受精作用的研究

短柄五加（ＥｌｅｕｔｈｅｒｏｃｏｃｕｓｂｒａｃｈｙｐｕｓＨａｒｍｓ．）开花当天,花药散粉,而雌配子体需经４～５ｄ才发育成熟。证实短柄五加为雄蕊先熟植物。开花第５天,成熟胚囊的比率为５７６９％,其余为退化和不育胚囊。开花第６天,胚囊开始受精。开花第１０天,受精胚囊占胚囊总数的５３５７％。柱头的可授期自开花后第４～５天开始,自花粉萌发至雌雄性核融合大约有２～３ｄ的间隔期。短柄五加受精过程与一般被子植物相同,其受精作用属于有丝分裂前配子融合类型。观察并统计了合子中雌性核仁的数目、存在状态,指出短柄五加合子中从雄性核仁出现到与雌雄性核仁融合为一个大核仁需经历３ｄ左右;如果以胚乳游离核数目为对照,大部分合子中雌雄性核仁的融合发生在３２～１２８个胚乳游离核时期。大多数合子是以雌雄性核仁融合为一个大核仁后进入合子分裂期;少数合子的雌雄性核仁不经融合也进入合子分裂期。观察到多精入胚囊、多精入卵以及成熟胚囊退化的现象。讨论了被子植物受精过程中有关受精终结的标志等问题。     

The Development of Gynoecium After Anthesis and Fertilization in Eleutherococcus brachypus (Araliaceae)

Eleutherococcus brachypus Harms. is a protandrous plant because the female gametophyte delays its maturation until the fifth day after anthesis and pollen shelling. On the fifth day after anthesis, about 57.69% of the embryo sacs matured and the rest degenerated or failed to develop. Fertilization began in the embryo sac on the fifth day. On the tenth day fertilization took place in 53.37 % of the total of embryo sacs. The stigma became receptible after 3 to 4 days of anthesis. It took 2 to 3 days from the germination of pollen grains on stigma to the fusion of male and female nuclei. The process of fertilization in E. brachypus is not different from most other angiosperms. It belonged to the type of premitotic syngamy. The observations and statistical analysis were made on the number feature of male and female nucleoli in the zygote. The result indicated that it took three days or so from the appearance of male nucleolus in the zygote to its fusion with the female nucleotus. Refering to the number of free nuclei of the endosperm, the fusion of male and female nucleoli in most of the zygotes occurred in the stage of 32 to 128 nuclei of the endosperm. Most zygotes con-tained a big nucleolus resulting from the fusion of male and female nucleolus and proceeding to mitosis. A few without fusion could also proceed to the mitotic stage. Features of multiple sperms entering the embryo sac or entering the egg cell and the degeneration of mature embryo sacs were observed as well. The sign of the termination of fertilization in angiosperms was discussed.     

Development of male and female flower in Asparagus officinalis. Search for point of transition from hermaphroditic to unisexual developmental pathway

Asparagus officinalis is a dioecious plant. The flowers start to develop as hermaphrodites and later become unisexual. In female flowers the stamens degenerate, while in male flowers the ovary stops growing without degenerating. We have examined young asparagus flowers using SEM and optical microscopy in order to determine the exact moment of transition from hermaphroditic to unisexual development. We defined 13 stages of development, starting from flower primordia up to completely mature flowers and labelled them with numbers from -6 to 7. The first five stages are fully hermaphroditic: a difference between sexes becomes visible at stage — 1 when the style begins to develop in female flowers. Degeneration of stamens in female flowers starts somewhat later. At the stage of transition, some differences between sexes also appear in the bidimensional polypeptide pattern of flowers. RNase activity shows a distinct peak at this stage (in female flowers only), probably related to stamen degeneration.     

Studies on the Structure,Afterripening and Cytochemistry of Seeds in Eleutherococcus brachypus Harms

Seeds of Eleutherococcus brachypus Harms were flat-kidney-shaped and their seed coats were only composed of one layer of cells. Embryos with abundant protein in their cells were just at the heart-shaped stage and were capped by sacs formed from degenerating endosperm cells when seeds shed from their maternal plants. A large amount of stored protein grains and lipids existed in endosperm cells but no polysaccharide grains were present either in endosperm cells or in embryo cells. Viable seeds were only 9.27% of the total. The plump seeds germinated in the cultivated field after 18～19 months and their germinating rate was 1.67%. Besides, the content of protein decreased gradually and a few polysaccharide grains were stored in embryo cells during the process. The afterripening process of seeds stratified at different temperatures ended after 6 months and the cytochemistry features of the seeds were that the content of protein decreased gradually and numerous polysaccharide grains had been stored in embryo cells at the late heart-shaped embryo stage and retained till the mature embryo stage. The structure, afterripening and cytochemistry of seeds were compared between Eleutherococcus brachypus and Eleutherococcus senticosus. The poor quality of the seeds, longer time of afterripening in a natural state and much lower germination rate of E. brachypus are considered to be important reasons for the endangerment of this species. Somemeasures are suggested for its conservation based on the above facts.     

MORPHOLOGICAL STUDIES OF THE NYMPHAEACEAE. XII. THE FLORAL BIOLOGY OF CABOMBA CAROLINIANA

Observations have been made on the pollination ecology of Cabomba caroliniana Gray in Texas. Flowers are trimerous with morphologically similar perianth parts. The adaxial corolla spurs are nectariferous and attract small Diptera (e.g. Notiphila cressoni and Hydrellia bilobifera). Anthesis occurs for 2 consecutive days with flowers opening about 10:00 a.m. and closing around 4 p.m. on each day. First-day flowers have short, indehiscent stamens and longer pollen-receptive stigmata which arch outward over the nectaries. In 2nd-day flowers the stamens have elongated to the level of the stigmata and extrorse dehiscense occurs above the nectaries. Stigmata of 2nd-day flowers are pressed together at the center of the flower and are nonreceptive to pollen. Insects attracted to 2nd-day flowers in search of nectar become dusted with pollen (due to the position and extrorse dehiscence of the anthers) and as insects fly to 1st-day flowers, achieve cross-pollination by virtue of the stigmata position over the nectaries. Seed anatomy is similar to that of other nymphaeaceous genera (i.e., abundant perisperm, little cellular endosperm, a haustorial nucellar “tube,” and a small dicotyledonous embryo). Pollination morphology and comparative xylem anatomy support the segregation of Cabomba from the Nymphaeaceae, sensu stricto. The anatomical correlations between seeds and the myophilous pollination syndrome (found elsewhere in Nymphaeaceae, sensu lato), however, suggest a phyletic relationship.     

The Fertilization and Early Development of Embryo and Endosperm in Stevia rebaudiana Bertani

The mature embryo sac is surrounded by endothelium tapetum. It is composed or an egg apparatus, one central cell with secondary nucleus, and 1–6 antipodal cells. About the 6th hour after pollination, female and male nuclei fuse with each other. The syngamy occurred almost simultaneously with the fusion of an other sperm nucleus and the secondary nucleus, but the velocity of the latter is faster than that of the syngamy. The fertilization of Stevia rebaudiana Bertani belongs to the premitotic type. About the 8th hour after pollination, primary endosperm nucleus is in mitosis, its dividing orientation may parallel or at right angle to the long axis of the embryo sac, and gives rise to two initial endosperm cells. The first five divisions of the endosperm cells are of synchronism. At the stage of heart-shaped embryo, the endosperm cells show the signs of digestion and absorbed. The endosperm development is of the cellular type. About the 10th hour after pollination, zygote divides for the first time. The division of the zygote is always transverse. The embryo development conforms to the Asterad type.     

Embryological Studies on Endangered Ophiopogon xylorrhizus (Liliaceae)

The embryological studies on an endangered species Ophiopogon xylorrhizus are reported in this paper. The anther was four-sporangiate, and its wall was composed of four layers: epidermis, fibrous endothelium, middle layer and glandular tapetum. Cytokinesis of microspore mother cell in meiosis was of the Successive type, and tetrads were tetrahedral or isobilateral. The mature pollen grains were 2-celled. Ovules were anatropous, bitegminous, and crassinucellate. Ovary wall ruptured 4～5 days after fertilization. The development of embryo sacs conformed to the Polygonum type. The two polar nuclei fused into a secondary nucleus before fertilization. The embryogeny was of the Asterad type, and endosperm development corresponded to the Nuclear type. About 55.8 % individuals in the population of O. xylorrhizus were found male sterile, and 43.3% of embryos aborted at early development stage. As a conclusion, we consider that (1)the failure of the xenogamy resulted from male sterility, autogamy and inefficient pollination agents, (2)embryo abortion and (3)exposure of young seeds during their early development are the weak links in the sexual reproductionof O. xylorrhizus, which would contribute to the endangerment of this species.     

Pre-zygotic embryological characters ofPlatycrater arguta, a rare and endangered species endemic to East Asia

Platycrater arguta Sieb. et Zucc. is a rare and endangered species endemic to East Asia. It produces two floral morphs viz. bisexual and male flowers. For bisexual flowers, simultaneous cytokinesis in the microsporocyte meiosis leads to a tetrahedral tetrad. The mature pollen grain is shed at 2-cell stage. The young anther wall is composed of epidermis, endothecium that develops fibrous thickenings at maturity, 1–2 middle layers and tapetum. The tapetum with uninucleate to binucleate cells, disintegrates in situ (glandular tapetum), yet in a small percentage of the anthers (about 37.6%), the tapetum does not disintegrate, causing complete male sterility. The ovules are anatropous, unitegmic, tenuinucellar and the formation of the embryo sac follows the monosporic, Polygonum type. Antipodal cells are lacking in the mature embryo sacs. Before fertilization, two polar nuclei fuse into a secondary nucleus. The formation of microsporangial wall, microsporogenesis and male gametogenesis in male flowers are analogous to those in the bisexual. Prezygotic embryological characters ofP. arguta were reported for the first time, revealing that its endangerment is correlated with the abortion of pollen of a part but not to the female development that is normal.     

The Fusion of Male and Female Nuclei in Fertilization of Higher Plants

Studies on the fusion of male and female nuclei in fertilization of Helianthus an- nuus L., Triticum aestivan L., Gossypium hisutum L., Hosta caerulea Tratt., and Pinus tabulaeformis Carr. were made in the present work. The results are summarized as follows: 1. The essential process of the fusion of male and female nuclei during syngamy in four species of angiosperms studied may' be generalized as follows: (1) the male nucleus made contact with the female one, (2) followed by the fusion of nuclear membranes between the male and female nuclei. (3) then the despiralization of male spireme happened and male nucleolus made its appearance inside of the fertilized egg nucleus (4) the male chromatin dispersed and make its appearance indistinguishable from that of the female chromatin, (5) the male and female nucleoli fused together to form a larger nucleolus as a sign of completion of the fusion of the two nuclei. In the first mitotic division of the zygote there was only one common mitotic spindle. 2. The essential process of the fusion of egg and sperm nuclei during syngamy in a gymnosperm-Pinus tabulaeformis could also be outlined as follows: (1) the sperm nucleus made contact with the egg nucleue, (2) the fusion of nuclear membranes happened between the male and female nuclei, (3) the male and female ehromatins condensed to form two separate groups of chromatin threads together with the very apparent apperance of the male and female nucleoli at this stage, (4) the male and female chromosomes grouped respectively in their own spindles while both nucleoli disappeared, (5) then the two spindles fused together and all the chromosomes arranged to form a common equatorial plate, (6) finally two daugter nuclei resulted from the mitotic division. 3. Based on the facts that there were two different patterns of the fusion of male and female nuclei in fertilization discribed, all of these accounts are in general accord with the condition usually described that there are two types of fertilization, the pre- mitotic and postmitotie syngamy in higher plants. The type of angiosperm fertilization and the mechanism of promoting the zygote to divide after fertilization are discussed, and the nuclear fusion in sexual reproduction has been compared with that of somatic cell hybridization.     

Study of Specific Protein on Sex Differentiation of Momordica charantia

In Momordica charantia L. the soluble protein profile of flower bud at hermaphroditic stage and three early developmental stages (the 7th, 10th and 13th day after initial budding) of male and female flowers were analysed with capillary electrophoresis. Some specific proteins related to sex differentiation were detected. The 11 kD protein, which appeared at the 7th day of budding and existed through the three developmental stages of the female flowers with little change of content, might be an "essential protein" for the expression of female flower differentiation program. Similarly, the 30 kD protein might be an "essential protein" for the expression of the male flower differentiation.     

Isolation of embryo sacs from Dianthus ovules by enzymatic treatments and microdissection

 Mature ovules of Dianthus (Caryophyllaceae) were histologically observed by clearing and serial sectioning to characterize the cells of the embryo sac. The results show that the mature embryo sac was located deep inside the hemitropous ovule due to thick nucellar tissue at the micropylar region. For the isolation of the embryo sacs, ovules were collected from ovaries of flowers 1 day after anthesis, and treated with an enzyme solution for digesting cell walls on a gyratory shaker. After 12 h of enzyme treatment, these ovules were dissected using a glass needle under an inverted microscope to release the embryo sacs. The embryo sacs, characterized by their specific size, were successfully released by these successive treatments. The viability of the embryo sacs was more than 80% as assessed with fluorescein diacetate staining. Fluorescent staining with 4,6-diamidino-2-phenylindole revealed the nuclei of the egg apparatus in the isolated embryo sacs. The procedure for isolating embryo sacs established in this study will offer a new approach to further in vitro studies on fertilization in Dianthus. Received: 20 January 1999 / Revision received: 12 July 1999 / Accepted: 17 August 1999     

Calcium changes in ovules and embryo sacs of Plumbago zeylanica L.

Calcium was localized in ovules of Plumbago zeylanica from 1 day before anthesis to 3 days after anthesis using potassium antimonate and transmission electron microscopy in pollinated and emasculated flowers. At 1 day before anthesis, embryo sacs (containing an egg cell, a central cell and zero to three accessory cells) appear mature and contain abundant calcium precipitates (ppts), in contrast to nucellar cells. At anthesis, the vacuoles of nucellar cells have enlarged, and micropylar cells, in particular, are heavily labeled with calcium ppts. As pollen tubes elongate through ovular tissues, ppts diminish in ovular cells and become concentrated in the pollen tube cell wall. After fertilization, the calcium ppts sharply diminish in fertilized ovules; in unfertilized ovules, calcium ppts remain abundant up to 3 days after anthesis (when unfertilized ovules are shed). The distribution of calcium in the ovule changes in apparent response to fertilization, suggesting that calcium content may be related to the attraction and receipt of the pollen tube. In contrast with conventionally-organized embryo sacs with synergids, Plumbago accumulates calcium in the egg cell. Received: 30 December 1999 / Revision accepted: 24 March 2000     

In Vitro Embryogenesis in Unfertilized Embryo Sacs of Oryza sativa L.

Haploid rice plantlets were induced from cultured ovaries in our previously reported experiment. The present paper is an embryological study on this subject. Young flowers of two japonica cultivars were excised and cultured just in the same manner as before. Liquid medium used for float culture was N6+3% sucrose+0.125 ppm MCPA. The inoculated materials were checked to be at late uninuclcate pollen stage which corresponded mainly to the uuinuelcate embryo sac stage, but as well as some 2- or 4-nucleate embryo sacs. Samples were fixed at 23 days intervals in acetomethanol (1:3), stained in toto with diluted Ehrlich's hematoxylin and sectioned by paraffin method for microscopical observation. 4 days after inoculation most of the embryo sacs developed up to 8-nucleate stage with polarized differentiation of the egg apparatus, central cell and antipodals. From 7th day on, proembryos of various sizes and shapes appeared in the micropylar region of some embryo sacs; some consisted of meristcmatic ceils, others were highly vacuo]ated. One-celled as well as linear multicellular suspensors atypical of in vivo zygote proembryos were observed, ttowever, it was uncertain whether the proembryos originated from the egg cell, the synergids, or the differentiating egg apparatus as a whole. Another peculiar event occured during culture was the formation of endosperm-like free nuclei from the unfertilized polar nuclei in some embryo sacs. Sometimes the free nuclei were numerous and showed a tendency of cell formation in localized areas. 12–15 days after inoculation, the proembryos developed into mieroseopieal ealli with globular or pearlike shape, wbieh continued enlarging to visible size with naked eyes at about 18–24 th day. Further growth eventually led the ealli protruding out the ovary wall beyond 32–35 the day. These observations indicate that the embryo sue, similarly as the pollen, can be induced to embryogenesis in vitro. This may open a new way to study the mechanism controlling gametophytie and sporophytie developmental pathways of embryo sac and provide means for large-scale production of "embryo sac plants" in future.     

WHY HERMAPHRODITIC PLANTS PRODUCE MANY MORE FLOWERS THAN FRUITS: EXPERIMENTAL TESTS WITH AGAVE MCKELVEYANA

Five hypotheses explaining the low fruit-to-flower ratios in self-incompatible hermaphroditic plants are tested for Agave mckelveyana. Results from pruning, bagging, and hand-pollination experiments indicate that “excess” flowers (i.e., flowers that fail to produce mature fruits) do not contribute to female fitness (i.e., fruit or seed production). These flowers are aborted regardless of their pollination history. Additional data on nectar production imply that these flowers act as pollen donors and contribute to male fitness.     

Floral herbivore effect on the sex expression of an andromonoecious plant,Isomeris arborea (Capparaceae)

Flower-feeding insects may influence the reproductive behavior of their host plant. In plants with labile sex expression, the ratio of maternal to paternal investment may change in response to damage, an effect that goes beyond the direct reduction of plant gametes. We examined the effects of floral herbivory by the beetle Meligethes rufimanus (Nitidulidae) on the ratio of hermaphroditic flowers to male flowers in an andromonoecious shrub, Isomeris arborea (Capparaceae) in southern California. Plants exposed to herbivory had a greater rate of flower bud abortion than those protected from herbivory. Exposed plants produced a greater proportion of hermaphroditic flowers to male flowers, although damaged inflorescences still produced fewer fruit. An additional manipulative experiment showed that the removal of pistils on inflorescences led to an increase in the proportion of hermaphroditic flowers. This suggests that the presence of fruit may lead to pistil suppression in developing flowers. Adaptive responses to herbivory which favor andromonoecy thus include the continued production of hermaphroditic flowers when floral damage is high (and hence low fruit set), and a switch to male flower production when floral damage is low (and fruit production increases). The consequences of an altered six ratio induced by insect herbivores may lead to indirect effects on both the male and female reproductive success of this plant.     

Function and evolution of sterile sex organs in cryptically dioecious Petasites tricholobus (Asteraceae)

Background and Aims

Why are sterile anthers and carpels retained in some flowering plants, given their likely costs? To address this question, a cryptically dioecious species, Petasites tricholobus, in which male and female plants each have two floret types that appear pistillate and hermaphroditic, was studied. The aim was to understand the function of sterile hermaphroditic florets in females. In addition, the first examination of functions of sterile female structures in male plants was conducted in the hermaphroditic florets on males of this species. These female structures are exceptionally large in this species despite being sterile.

Methods

Differences in floret morphology between the sex morphs were documented and the possible functions of sterile sex organs investigated using manipulative experiments. Tests were carried out to find out if sterile female structures in male florets attract pollinators and if they aid in pollen dispersal, also to find out if the presence and quantity of sterile hermaphroditic florets in females increase pollinator attraction and reproductive success. To investigate what floret types provide nectar, all types of florets were examined under a scanning electron microscope to search for nectaries.

Key Results

The sterile female structures in male florets did not increase pollinator visits but were essential to secondary pollen presentation, which significantly enhanced pollen dispersal. Sterile pistillate florets on male plants did not contribute to floral display and disappeared in nearly half of the male plants. The sterile hermaphroditic florets on female plants attracted pollinators by producing nectar and enhanced seed production.

Conclusions

The presence of female structures in male florets and hermaphroditic florets on female plants is adaptive despite being sterile, and may be evolutionarily stable. However, the pistillate florets on male plants appear non-adaptive and are presumably in decline. Differential fates of the sterile sex organs in the species are determined by both the historical constraints and the ecological functions.     

Embryological study on gynogenesis in onion (Allium cepa L.)

Haploid induction in onion can, to date, be induced only via gynogenesis by culturing unfertilized flowers, ovaries or ovules. The process of haploid embryo induction has been macroscopically well studied, but only limited data exist from microscopic examination of ovule development status at the inoculation stage and of the origin of gynogenic embryos. Microscopic studies were carried out using individual donor plants with relatively high embryo induction frequencies (45.9 embryos formed per 100 flowers, on average, for 2 years). Ovaries from flower bud culture were fixed at 1 week intervals up to the 7th week of culture. These were compared with pollinated ovaries at 1 or 2 weeks after pollination. In total, 1428 unfertilized embryo sacs were examined. The results indicate that, at the time of inoculation, ovules within ovaries 2.0–3.0 mm in diameter contained two- or four-nucleate embryo sacs in the smallest ovaries to mature embryo sacs in the largest ovaries. It seems likely that the embryos are actually induced from ovaries cultured at the immature stage. After 1 or 2 weeks in culture, the egg apparatus primarily consisted of distinctly enlarged synergids and the egg cell, which was often detached from the micropylar pole. But free nuclear endosperm was also formed. From the 2nd to 7th week in culture, formation of haploid embryos (from globular to the almost mature cylindrical stage) was detected in 5.7% of the ovules. Their origin, for several reasons, was most likely the egg cell. In addition, ovules containing endosperm only (3.6%) and ovules containing the egg apparatus (0.5%) or both endosperm and embryo (0.4%) were detected. This observation is probably unique and has not yet been reported in other species studied. Received: February 2001 / Revision accepted: 20 April 2001     

Embryo sac development is affected in Petunia inflata plants transformed with an antisense gene encoding the extracellular domain of receptor kinase PRK1

 In a previous study of the function of a pollen-expressed receptor kinase of Petunia inflata, PRK1, it was found that transgenic plants carrying an antisense-PRK1 gene were unable to transmit the transgene through either the male or, unexpectedly, the female. In this report, the nature of this female phenotype was studied using one of the transgenic plants, ASRK-13. Electron and light microscopic examination of the embryo sac and seed development of ASRK-13 and a wild-type plant revealed that embryo sac development of approximately half of the ovules of ASRK-13 was abnormal. The development of the affected embryo sacs was arrested at the late stages of megagametogenesis. The majority of the affected embryo sacs completed three rounds of mitosis normally, but failed to progress through the maturation stages when cell expansion, nuclear migration, and differentiation take place. The remaining small number of abnormal embryo sacs were arrested at either the four- or eight-nucleate stages. The ovules containing the defective embryo sacs apparently failed to be fertilized, resulting in degeneration of half of the seeds produced by ASRK-13. RNA gel blot analysis suggests that the PRK1 gene is expressed in the ovary, albeit at a much lower level than in the anther. The possibility that the antisense PRK1 gene is responsible for the abnormal embryo sac development is discussed. Received: 25 April 1997 / Revision accepted: 25 June 1997     

小盐芥受精作用和胚发育的解剖学研究

用石蜡切片法对小盐芥(Thellungiella halophila(C.A.Mey.)O.E.Schulz)的受精作用及胚和胚乳的发育过程进行了解剖学观察,结果显示:花盛开前后,是受精作用的核融合时期;受精前,2个极核融合成次生核;受精作用属有丝分裂前型;胚乳发育为核型;胚发育属柳叶菜型,子叶背倚胚根;成熟种子无胚乳.