An Ultrastructural Study of The Embryo/Endosperm Interface in the Developing Seeds of Solanum nigrum L. Zygote to Mid Torpedo Stage

The early developmental sequences in the formation of the Zoneof Separation and Secretion in a hexaploid species of Solanumnigrum L. are described. Ultrastructural changes which occurredduring the development of the embryo/endosperm interface couldbe related to the different stages in the embryo's development.The first step was the completion of the cell wall around thechalazal end of the zygote; a thin wall was formed along theendosperm cell(s) abutting the zygote. From the mature zygotestage to the quadrant stage, minute plasmalemma invaginationsoccurred along the endosperm wall facing the zygote. These invaginationsenlarged, and from the mid-globular stage onwards became filledwith a fine fibrillar material; this material accumulated betweenthe endosperm cell wall and the plasmalemma before being releasedinto the developing periembryonic and intercellular spaces tobecome the extracellular matrix. Cell wall development in theendosperm cells abutting the embryo followed an unusual path.During the quadrant stage, whilst the outer embryo wall increasedin thickness due to vesicle fusion, the endosperm cell wallfacing the embryo showed a loosening of the wall fibrils aswell as partial separation of these same endosperm cells fromeach other. From the early-globular stage, the endosperm cellwalls opposite the embryo became electron-translucent, disappearinginto the extracellular matrix. Enzymic secretions by the embryomay account for the alteration in the abutting endosperm cellwalls. Enzymic activity may also explain the development ofa homogenous electron-opaque layer over the outer embryo wallas well as the differences in the width of the fibrillar layerwhich accumulated around the cotyledons as the embryo grew throughthe Zone of Separation and Secretion. The potential roles ofthe extracellular matrix are briefly discussed. Solanum nigrum L.; embryo/endosperm interface; Zone of Separation and Secretion; embryo development; cellular endosperm     

The Initiation, Development and Removal of Embryo Sac Wall Ingrowths in the Developing Seeds of Solanum nigrum L. An Ultrastructural Study

In developing seeds of Solanum nigrum L., wall ingrowths developedat the extreme micropylar and chalazal ends of the embryo sac.In the micropylar region, the wall ingrowths were initiatedat the three-celled endosperm stage starting at the base ofthe zygote then progressing for a short distance chalazalwards.They developed quickly with the most elaborate around the baseof the suspensor. The chalazal wall ingrowths developed alongthe surfaces of the chalazal cup, the antipodal cup and thehypostase. Those along the hypostase were initiated at the four-celled,those in the chalazal and antipodal cups at the 20-celled endospermstages. The most elaborate developed along the base of the antipodalcup; the most simple were along the base of the chalazal cup.Small electron-lucent invaginations of the plasmalemma whichlater became filled with fibrillar material, were the earliestindication of wall ingrowth formation. Removal of the wall ingrowthscommenced at the mid-globular stage of embryo development andwas completed by the mid-heart-shaped stage. In the micropylarregion, wall ingrowth removal was rapid, starting with the lossof the fibrillar component followed by the thinning of the cellwall. However, along the hypostase and antipodal cup, a heterogeneouslayer of varying electron densities and a thinner, more electrondense layer was laid down over the ingrowths. This was followedby the removal of the fibrillar component. The initiation, removaland location of the embryo sac wall ingrowths is discussed inconnection with understanding the nutritional relationshipsbetween maternal tissue, endosperm and embryo.Copyright 1995,1999 Academic Press Wall ingrowths, Solanum nigrum, transfer cells, zone of separation and secretion, hypostase     

Localization of Phenolic Compounds in the Covering Tissues of the Embryo of Brassica napus (L.) during Different Stages of Embryogenesis and Seed Maturation

During embryogenesis and maturation of an embryo the tissuescovering it produce phenolic compounds the localization of whichchanges during maturation of the embryo. In the ovary containinga globular embryo, phenolics are located in the epidermis ofthe integumentum externum and the innermost layer of the integumentuminternum. In the ovule at the stage at which heart- and torpedo-shapedembryos are present, phenolic compounds are visible in the stellarcells, the innermost cells of the integumentum internum andthe endosperm. In hard, green seeds, after the integumentuminternum and layers over the stellar cells gradually disappear,the remaining tissue contains cell walls impregnated with phenolics.Mature, black seeds contain only one distinct layer of cells—stellarcells, which, like the other compressed cell walls, are impregnatedwith phenolics. In this way they constitute a barrier betweenthe embryo and its environment.Copyright 1994, 1999 AcademicPress Brassica napus, seed coat, integumentum, phenolic compounds     

Embryo and Endosperm Function and Failure inSolanumSpecies and Hybrids

Although the importance of the endosperm as a food store inmany angiosperm seeds is well known, its significance duringearly embryogenesis has been neglected. In many interspecifichybrids, and in some other situations, embryos do not developfully and abort. It has often been stated that this is causedby the endosperm failing to conduct sufficient nutrients tothe embryo, but seldom has it been suggested that the endospermactively controls most of the early stages of morphogenesisof the embryo. Information gleaned from a broad survey of theliterature, combined with additional evidence presented here,obtained fromSolanum incanumand interspecific hybrids, indicatethat the endosperm is dynamic and very active in regulatingearly embryo development. This requires highly integrated geneticcontrol of rapidly changing metabolism in the endosperm. Ininterspecific hybrids, lack of coordination may cause unbalancedproduction of growth regulating substances by the endospermand hence abortion of the embryo, or even unregulated productionof nucleases and proteases resulting firstly in autolysis ofthe endosperm and then digestion of the embryo. The endospermmay thus serve to detect inappropriate hybridization of speciesor ploidy levels and so prevent waste of resources by producingseeds that would result in sterile hybrids or unthrifty subsequentgenerations. This discriminatory function of the endosperm hasdiminished during evolution and domestication of the crop plantSolanummelongenaL.Copyright 1998 Annals of Botany Company Solanum, embryo morphogenesis, endosperm, hybrid, seed development.     

Localization of ATPase Activity on the Plasmalemma of Scutellar Epithelial Cells of Germinating Barley (Hordeum vulgare L.)

Chaffey, N. J. and Harris, N. 1985. Localization of ATPase activityon the plasmalemma of scutellar epithelial cells of germinatingbarley (Hordeum vulgare L.).—J. exp. Bot 36: 1612–1619. ATPase activity has been localized at an ultrastructural levelin the absorptive region of the scutella of germinating barley(Hordeum vulgare L.). The enzyme is localized on the plasmalemmaof the epithelial cells. Using the Gomori reaction the depositionof reaction product on the plasmalemma, which is dependent uponthe presence of supplied ATP, was precluded or reduced by theinhibitors orthovanadate, mercuric chloride and DCCD, whilstß-glycerophosphate would not act as an alternativesubstrate. The mitochondria demonstrated phosphatase activitywith both ATP and ß-glycerophosphate as substrate.The results are discussed in relation to the active uptake ofmetabolites by the scutellum during germination and the structuralmodification of the plasmalemma of the epithelial cells to formplasmatubules. Key words: ATPase, Hordeum vulgare L., localization (ultrastructural)     

Nature of 'Pollinator' Effect in Potato (Solanum tuberosum L.) Haploid Production

Haploids (2n =24) of the common tetraploid (2n=48) potato (SolanumtuberosumL.) provide promising material for attacking many problemsconcerned with the genetics, cytogenetics and breeding of thisspecies. Interspecific 4xx2xcrosses betweenSolanum tuberosumgp.Andigenaorgp.Tuberosumcultivars as pistillate parents andSolanum tuberosumgp.Phurejaassource of pollen (hereafter ‘pollinator’) have beenused to produce maternally derived haploids through parthenogenesis.This paper discusses the nature of the ‘pollinator’effect in haploid extraction. The ‘pollinator’ hada significant effect on haploid frequencies following 4xx2xcrosses.The ‘pollinator’ effect seems to operate via theendosperm, in which haploid (n=2x) embryos are associated withhexaploid endosperm. A superior ‘pollinator’ appearsto have its effect by contributing two haploid (n) gametes tothe central cell. 2n pollen; double fertilization; endosperm; ploidy manipulations; Solanum tuberosum     

Structure, Composition and Physiological State of the Endosperm of Phoenix dactylifera L

The date endosperm consists of living cells with the same generalcellular structure throughout the seed. The major storage products,as shown by histochemical staining, are lipid, stored as numeroussmall lipid bodies which fill the cytoplasm, and protein, aslarge but variably-sized protein bodies. Nuclei are presentbut lack large amounts of heterochromatin. Plastids and mitochondriaare present but infrequently seen and have poorly developedinternal membranes. No endoplasmic reticulum or dictyosomesare present before or after hydration. The cell wall is thickexcept in areas of pit fields and consists of three layers whichdiffer in their staining behaviour: middle lamella, thickenedwall and inner wall. Both the endosperm and embryo of the imbibedseed undergo aerobic respiration, but the embryo respires ata more rapid rate than does the endosperm. A small area of theendosperm around the distal pole of the cotyledon shows histochemicallydetectable levels of succinic dehydrogenase. Phoenix dactylifera L, date palm, endosperm, ultrastructure, histochemistry, respiration, succinic dehydrogenase     

Production and secretion of {alpha}-galactosidase and endo-{beta}-mannanase by carob (Ceratonia siliqua L.) endosperm protoplasts

Viable protoplasts were isolated for the first time from maturecarob (Ceratonia siliqua L.) endosperm tissue. After 5 d ofincubation 75% of the protoplasts were viable. During incubationthey underwent vacuolation and produced the carob endospermhydrolases, agalactosidase and endo-ß-mannanase, whichwere secreted in the incubation medium. The secretion of bothenzymes were under Ca²⁺ control. Many characteristics of -galactosidaseand endo-ß-mannanase production by protoplasts werethe same as those of whole endosperms: their production didnot require any hormonal signal and was inhibited in the presenceof ABA or the leachate from the carob endosperm/seed coat. Moderatewater stress (—2.0 MPa) neither affected the activityof these hydrolases nor their secretion by endosperm protoplast.However, when the osmoticum of protoplast incubation mediumwas higher, the production and secretion of both hydrolaseswere reduced. Comparison of the hydrolases activities in theincubation media of leached carob endosperms, which were incubatedunder normal and water stress (—1.5 MPa) conditions, withthe activities of the protoplast-secreted hydrolases indicatedthat (i) carob endosperm cell wall acts as a barrier for thesecreted enzymes and (ii) that water stress reduces the cellwall porosity of the carob endosperm cells, and thus the releaseof the secreted -galactosidase and endo-ß-mannanaseis inhibited. The isolation of carob endosperm protoplasts offersa potent experimental system for the study of aspects of endospermcell physiology, such as enzyme secretion Key words: Abscisic acid, carob endosperm, Ceratonia siliqua L, endo-ß-mannanase, -galactosidase, leachate, protoplasts, water stress     

Studies on Mature Seeds of Cuscuta pedicellata and C. campestris by Electron Microscopy

The seeds of Cuscuta pedicellata have been investigated by transmissionand scanning electron microscopy. Additional observations havebeen made on seeds of C. campestris by SEM only. The seed coatconsists of an outer single epidermis, two different palisadelayers, and an inner multiparenchyma layer. The outer epidermalwall in C. pedicellata has a thick cuticle and zones rich inpectic substances. The thicker ‘U-shaped’ cell wallsin the outer palisade layer are strengthened by a wall layerof hemicellulose. The inner palisade layer has thick walledcells with a ‘light line’. The inner cell wall ofthe compressed multiparenchyma layer has a thin cuticle. A fairlythick cuticle is positioned directly on the endosperm surface.The aleurone cell walls are different from the remaining endospermwalls. The latter are thick and believed to be of galactomannans.There is a ‘clear’ zone between the plasmalemmaand the cell wall in the aleurone cells. The embryo cells arepacked with lipids and proteins. In Cuscuta campestris mostendosperm has been absorbed during the seed development. Theembryo apex has two minute leaf primordia. The features of theCuscuta seeds are discussed in relation to functional and environmentalconditions. Cuscuta pedicellata, Cuscuta campestris, seed, seed coat, cuticle, cell walls, endosperm, aleurone cells, galactomannan, embryo, TEM, SEM     

Structure and In Vitro Growth of Zygotic Embryos of Taro (Colocasia esculenta var. antiquorum)

Zygotic embryos of taro, Colocasia esculenta var. antiquorumwere examined using both light and scanning electron microscopyand cultured on Linsmaier-Skoog (LS) medium without the additionof growth regulators. Embryos present within mature seed consistof a hypocotyl-root axis and an undeveloped cotyledon and aresurrounded by two major types of endosperm cells, aleurone andstarchy endosperm. Embryos cultured on LS medium developed intomature plants only in the presence of endosperm tissue. Excisedembryos turned green after 2–4 d in culture and reacheda rapid growth period between days 4 and 6. Culture of taroembryos leading to viable plantlet development depends upon(1) removal of the outer and inner integument, and (2) the presenceof endosperm tissue (including an intact aleurone layer). Colocasia esculenta var. antiquorum, Araceae, taro, embryo culture, integument, endosperm     

Influence of Irradiated Pollen on Embryo and Endosperm Development in Kiwifruit

Development of seeds following pollination with irradiated pollenwas studied inActinidia deliciosa(kiwifruit) ‘Hayward’.Pollinations were carried out using two different sources ofpollen (‘Tomuri’ and ‘Matua’) irradiatedwith gamma rays at doses of 700 and 900 Gy. Non-irradiated crosseswere used as controls. Pollen irradiation had little effectonin vitropollen germination. Irradiated pollen affected seedset and seed content, and induced the formation of parthenogeneticembryos. In comparison to the control, the embryo growth ratewas slower and the endosperm contained very low amounts of storageproducts. Seed set was significantly reduced following bothdoses of irradiation. Two types of seeds were observed: (1)seeds with endosperm only; and (2) seeds with both embryo andendosperm. The proportion of seeds containing endosperm onlywas almost ten-fold higher than those containing both embryoand endosperm. Embryo production by gamma-irradiated pollenwas genotype- and dose-dependent. The induction of parthenogenesiswas higher following gamma ray doses of 900 Gy than 700 Gy,which suggests the ‘Hertwig Effect’; the best efficiencywas obtained with ‘Tomuri’ pollen. Ploidy levelof parthenogenetic embryos was evaluated by nuclear size (area)with the use of image analysis. There was a large differencein embryo nuclei size between control and parthenogenetic embryos(mean size 90.8 and 49.1 µm², respectively). It is concludedthat parthenogenetic embryos represent trihaploids.Copyright1998 Annals of Botany Company. Actinidia deliciosa, kiwifruit, pollen irradiation, induced parthenogenesis.     

Cell Wall Degrading Enzymes in Cuscuta reflexa and Its Hosts

Pectin degrading enzymes, hemicellulose degrading enzyme andcellulose degrading enzymes were studied in Cuscuta reflexaRoxb., its susceptible hosts, Brassica campestris L., Cocciniaindica W. & A. Datura innoxia Mill, Helianthus annuus L.,Holoptelea indica Planch, Lantana camara L., Medicago sativaL., Manihot utilissima Pohl, Petunia hybrida X Hort exvilm,Pisum sativum L., Phaseolus vulgaris L. and Solanum nigrum L.and non-susceptible plants Ipomoea batata Lam. and Solanum tuberosumL. Pectin esterase and polygalacturonase were present in higheramounts in Cuscuta parasitic on P. vulgaris and S. nigrum, whichneeded more time for haustorial establishment. Exo-l, 4-ß-D-glucosidaseactivity was found in Cuscuta but could not be detected in itshosts. Xylanase and cellulase activity of host plants increasedwhile cellobiase activity decreased as a result of infectionby the parasite. Higher pectin esterase, polygalacturonase,xylanase and exo-l, 4-ß-D-glucosidase activities inthe haustorial region of the parasite is likely to bring aboutthe lysis of the cell wall of the host plant and thus facilitatethe penetration of the parasite haustoria into the host sieveelement, which is necessary for the transport of nutrients betweenthe host and the parasite. Key words: Cell wall degrading enzymes, Cuscuta reflexa     

A Comparative Study of Early Seed Development in Genotypes of Barley and Rye

Early seed development was studied in 17 genotypes of barley,Hordeum vulgare L., and 11 genotypes of rye, Secale cerealeL. The numbers of cells and nuclei in the embryos and endospermsof developing seeds were scored daily for 5 days after selfpollination. For embryos, the mean cell doubling times variedfrom 9.2–12.9 h for barley and 15.7–22.7 h for rye.Endosperm mitotic cycle times of both species were shortestover the first 24 h after pollination but then became longer.A non-linear correlation was found between the number of embryocells and the number of endosperm nuclei in barely and rye andis similar to that for other members of the Triticeae. Hordeum vulgare L., Secale cereale L., barley, rye, embryo, endosperm, mean cell doubling time     

Changes in Properties of Malate Dehydrogenase Isolated from Solanum nigrum L. Seeds Imbibed at High Temperatures

Exposure of Solanum nigrum L. seeds for 48 h to high temperature(50°C) during imbibition, lowered considerably the activityof malate dehydrogenase in the mitochondria and in the cytosol.The affinity of both isozymes for their substrates and co-enzymeswas strongly depressed by this treatment. Optimal pH and optimaltemperature for maximal specific activity were also changed.Enzyme from treated seeds, although much less active, was moreheat tolerant. Separation on a DEAE cellulose column showedtwo distinct peaks of activity for cytosolic malate dehydrogenasefrom both treated and control seeds. Gel filtration througha G-75 Sephadex column showed only one peak of activity in bothcases. Gel electrophoresis of s-MDH from control seeds showedtwo bands of enzyme activity for each of the peaks eluting fromthe DEAE column. Only one activity band could be detected forenzyme from heat treated seeds and this band corresponded toone of the activity bands found in the control. From analysisof the data it appears that while part of the enzyme was denatured,due to exposure of the seeds to 50°C, a conformational changein the other part of the enzyme might have occurred which resultedin a change of enzyme properties and activity. However, on thebasis of the reported results an induction of synthesis of anew ‘heat tolerant’ enzyme, due to the treatment,cannot be ruled out. Key words: Solanum nigrum L., malate dehydrogenase, heat treatment, seeds     

Two Types of Embryo Sac Development in Scrophularia himalensis Royle

The development of the embryo sac in Scrophularia himalensisRoyle (tribe Cheloneae, Scrophulariaceae) has been investigated.The ovules are anatropous, unitegminal and tenuinucellar. Twotypes of embryo sac development—the monosporic (polygonumtype) and the bisporic (allium type)—coexist in this species.This is the first record of its kind in Scrophularia as previousworkers reported only the Polygonum type of development in thetribe Cheloneae.     

Absorption and Secretion of Polyethylene Glycol by Solanaceous Plants

The response of the following species of the Solanaceae to waterstress caused by polyethylene glycol (PEG) as an osmoticum,was examined: Solatium khasianum, S. laciniatum, S. melongena,S. nigrum, S. tuberosum, Capsicum annuum, Lycopersicon esculentumand Hyosciamus boveanus. Secretion of solution from the leaveswas observed in these plants when put into 4.5% solution ofPEG 1500, 4000 and 6000. Secretion of liquid started after 20min in seedlings with mechanically damaged roots, and after24 h in plants with intact roots. After evaporation of the liquid,deposits of white material which remained on the leaves wereidentified as PEG by high pressure liquid chromatography andby PEG induced protoplast fusion. All the species examined bear glandular and non-glandular hairson their leaves. In species with leaves which are highly tomentous,PEG secretion took place mainly through the non-glandular hairs.In species with a small number of hairs, secretion took placethrough ordinary epidermal cells. Under similar conditions mannitolsolution was secreted only through wounds and cracks, and NaClsolution was not secreted at all. Key words: Secretion, PEG, Solanaceous plants     

Establishment, Structure and Morphology of the Tuber of Balanophora

During germination of the ‘seed’ of Balanophora,endosperm cells at the radicular pole grow out as tubular structuresand anchor the ‘seed’ to the host rootlet. The radiculartier of cells of the embryo elongate as primary haustorial tubesand establish contact with the host root vasculature. A secondaryhaustorium arises from a meristem adjoining the primary haustorium.The remainder of the embryo contributes to the tuber proper. Host parenchyma in the immediate vicinity of the primary haustoriumreverts to meristematic activity. Some of the derivatives matureas perforate tracheary cells. The remainder, retaining meristematicactivity, squeeze themselves between secondary haustorial cellsand together initiate a composite conducting strand, which repeatedlydichotomizes as the tuber grows. The conducting strand of Balanophora is looked upon as the equivalentof combined adventitious root system of parasite and host. Theremaining part of the tuber is equivalent to the shoot. Balanophora, tuber, morphology, host-parasite relations, parasite     

Histochemical and Ultrastructural Observations on the Nacreous Walls of the Sieve Elements of Atrichum undulatum

The nacreous walls of the sieve elements of Atrichum undulatumare composed of a loose fibrillar matrix. Histochemically, thesewalls have cellulose, pectins, proteins, phospholipids, andRNA as components. Ultrastructurally, the walls contain fragmentsof the plasmalemma and what appear to be aggregations of endoplasmicreticulum and vesicles. The unusual presence of these cytoplasmiccomponents appears to explain the positive histochernical testsfor proteins and RNA.     

An Analysis of Seed Development in Pisum sativum III. The Relationship Between the r Locus, the Water Content and the Osmotic Potential of Seed Tissues in vivo and in vitro

The water content and osmotic potential (₂) of the differentparts of the pea fruit have been measured during developmentof the seed in two lines near-isogenic except for the r locus.During the early development of both genotypes, the testa possesseda more negative ₂ than either embryo, endosperm or pod while,at stages when liquid endosperm was present, the embryo alwaysmaintained ₂, more negative than the endosperm. A clear effectof the r locus on water content and ₂ was only observed in embryotissue — wrinkled (rr) embryos possessing more water andmaintaining a more negative ₂ than round (RR) for most of thedevelopmental period studied. The more negative ₂ of wrinkledembryos correlated with their greater uptake of water in vivo. When cultured in vitro, the embryos of both genotypes showedmaximum growth (fresh or dry weight) if 10 per cent sucrosewas added to the medium (equivalent to about — 1.2 MPa).Round embryos, however, increased in weight more than wrinkledat all sucrose concentrations examined. Cultured embryos maintaineda similar or more negative ₂ than their surrounding medium;wrinkled more negative than round. Embryo culture, osmotic potential, Pisum sativum, pea, r locus, seed development, tissue culture, water content     

The Extrafloral Nectaries of Cotton: II. CYTOCHEMICAL LOCALIZATION OF ATPASE ACTIVITY AND CA2+ -BINDING SITES, AND SELECTIVE OSMIUM IMPREGNATION

Localization of ATPase activity in the extrafloral nectariesof cotton (Gossypium hirsutum) shows most pronounced granularstaining at the plasmalemma of the sieve tube companion cellsbelow the nectaries and at the plasmalemma of cells in the secretorypapillae, particularly in the apical cell. Staining was muchmore intense in mature, secreting nectaries than in young, non-secretingones. When CaCl₂ is included in the fixation and washing solutionswith the aim of localizing calcium binding sites, prominentamorphous electron dense globules are seen at the plasmalemmaof the cells in the papillae, but also associated with othermembranes. Both granular and amorphous deposits are seen whenstaining for Ca²⁺-ATPase activity. Selective osmium impregnationshows pronounced staining of the ER and nuclear envelope insecreting nectaries but not in young non-secreting ones. Key words: Adenosine triphosphatase, Gossypium hirsutum, Nectary, Secretion