Early Development of the Macadamia Ovary

1981 ◽  
Vol 29 (2) ◽  
pp. 185 ◽  
Author(s):  
M Sedgley
Keyword(s):  
Light Microscopy ◽  
Early Development ◽  
Cell Walls ◽  
Cell Formation ◽  
Embryo Sac ◽  
The Other ◽  
Globular Embryo ◽  
Macadamia Integrifolia

Macadamia integrifolia ovaries were sampled for light microscopy from anthesis to 8 weeks after flowering. Both ovules increased in size following anthesis but only one was normally fertilized. Fertilization of one ovule appeared to inhibit fertilization of the other. The unfertilized ovule was eventually crushed by the fertilized ovule which developed a globular embryo with a short suspensor. Division of the endosperm preceded division of the embryo, and cell formation in the initially free nuclear endosperm progressed by the development of cell walls inwards from the embryo sac wall at the micropylar end of the embryo sac only. Thickenings developed on the walls of the embryo sac, persistent synergid and embryo and a hypostase developed at the base of the nucellus between the cavity occupied by the embryo sac and the integument. Both specializations are suggested to be important in the nutrition of the developing embryo. Ovaries which abscissed 4-5 weeks after anthesis had a similar anatomy to ovaries retained on the tree. Some embryos showed signs of degeneration but this was not considered to be the cause of abscission.

Embryo sac development in soybean: cellularization and egg apparatus expansion

1990 ◽  
Vol 68 (10) ◽  
pp. 2135-2147 ◽  
Author(s):  
M. W. Folsom ◽  
D. D. Cass
Keyword(s):  
Ultrastructural Study ◽  
Cell Walls ◽  
Embryo Sac ◽  
Chain Structure ◽  
Mitotic Division ◽  
The Other ◽  
Synergid Cell ◽  
Egg Apparatus ◽  
Embryo Sac Development

An ultrastructural study of soybean embryo sac development was performed. Prior to the final mitotic division and cellularization a nuclear rearrangement occurs that involves the chalazal movement of one of the two micropylar nuclei. During cellularization this nucleus divides to form the egg and micropylar polar nuclei and produces the wall that separates the central ceil from title space occupied by the egg apparatus. Within this space the other nucleus divides to form the two synergid nuclei and one of the two walls that separate the egg and synergid cells from one another. Egg apparatus cells are initially densely cytoplasmic, each is enclosed by thick, highly dissected walls, and they are all similar with respect to distribution of organelles except that synergid nuclei are micropylar to the egg nucleus. There is a progressive thinning and segmentation of egg apparatus walls during cellular expansion until they resemble the beaded chain structure seen in the mature egg and synergid cell walls. Taken as a whole these observations suggest that the chalazal movement of one of the two micropylar nuclei during the 4-nucleate stage is pivotal in determining future patterns of egg apparatus development.

Ultrastructural observations of the mature megagametophyte and the fertilization in wheat (Triticum aestivum)

1985 ◽  
Vol 63 (2) ◽  
pp. 163-178 ◽  
Author(s):  
Ruilin You ◽  
William A. Jensen
Keyword(s):  
Triticum Aestivum ◽  
Pollen Tube ◽  
Cell Walls ◽  
Embryo Sac ◽  
Mature Embryo ◽  
Central Cell ◽  
The Other ◽  
Egg Cell ◽  
Filiform Apparatus ◽  
Egg Apparatus

The mature embryo sac of wheat contains an egg apparatus composed of an egg cell and two synergids at the micropylar end, a central cell with two large polar nuclei in the middle, and a mass of 20 to 30 antipodals at the chalazal end. A comparison was made of the ultrastructural features of the various cells of the embryo sac. The features included the position of the nucleus and vacuoles, the number, structure, and distribution of organelles, and the extent of the cell walls surrounding each cell. The pollen tube enters one synergid through the filiform apparatus from the micropyle. The penetration and discharge of the pollen tube causes the further degeneration of that synergid, which had already undergone changes before pollination. The second synergid does not change further in appearance following the penetration of the first by the pollen-altered tube. Half an hour after pollination at 20–25 °C, two male nuclei are seen in the cytoplasm of the egg and the central cell. At about 1 h after pollination, one sperm has made contact with the egg nucleus, while the other sperm is fusing with one of the polar nuclei.

Ectodesmata as Revealed By Freeze-Etch Preparations of Plant Epidermal Cell Walls

1973 ◽  
Vol 31 ◽  
pp. 468-469
Author(s):  
N.C. Lyon ◽  
W. C. Mueller
Keyword(s):  
Electron Microscopy ◽  
Acetic Acid ◽  
Nitric Acid ◽  
Oxalic Acid ◽  
Light Microscopy ◽  
Epidermal Cell ◽  
Cell Walls ◽  
Plant Viruses ◽  
Plant Leaves ◽  
Thin Sections

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.

Comparative strengths and weaknesses of peroxidase and colloidal gold in pre- and post-embedding immunolabeling techniques

1987 ◽  
Vol 45 ◽  
pp. 1002-1005
Author(s):  
D. R. Abrahamson ◽  
P. L. St.John ◽  
E. W. Perry
Keyword(s):  
Electron Microscopy ◽  
Horseradish Peroxidase ◽  
Light Microscopy ◽  
Colloidal Gold ◽  
Light Microscope ◽  
Ultrastructural Localization ◽  
The Other ◽  
Quantitative Studies ◽  
Dense Suspension ◽  
Antigen Localization

Antibodies coupled to tracers for electron microscopy have been instrumental in the ultrastructural localization of antigens within cells and tissues. Among the most popular tracers are horseradish peroxidase (HRP), an enzyme that yields an osmiophilic reaction product, and colloidal gold, an electron dense suspension of particles. Some advantages of IgG-HRP conjugates are that they are readily synthesized, relatively small, and the immunolabeling obtained in a given experiment can be evaluated in the light microscope. In contrast, colloidal gold conjugates are available in different size ranges and multiple labeling as well as quantitative studies can therefore be undertaken through particle counting. On the other hand, gold conjugates are generally larger than those of HRP but usually can not be visualized with light microscopy. Concern has been raised, however, that HRP reaction product, which is exquisitely sensitive when generated properly, may in some cases distribute to sites distant from the original binding of the conjugate and therefore result in spurious antigen localization.

scholarly journals Fetal erythropoiesis in steel mutant mice. III. Defect in differentiation from BFU-E to CFU-E during early development

Blood ◽  
1978 ◽  
Vol 51 (3) ◽  
pp. 539-547 ◽  
Author(s):  
DH Chui ◽  
SK Liao ◽  
K Walker
Keyword(s):  
Progenitor Cells ◽  
Early Development ◽  
The Other ◽  
Mutant Mice ◽  
Erythroid Progenitor ◽  
Erythroid Progenitor Cells ◽  
Other Hand ◽  
Colony Forming Units ◽  
Fetal Erythropoiesis

Abstract Erythroid progenitor cells in +/+ and Sl/Sld fetal livers manifested as burst-forming units-erythroid (BFU-E) and colony-forming units- erythroid (CFU-E) were assayed in vitro during early development. The proportion of BFU-E was higher as mutant than in normal fetal livers. On the other hand, the proportion of CFU-E was less in the mutant than in the normal. These results suggest that the defect in Sl/Sld fetal hepatic erythropoiesis is expressed at the steps of differentiation that effect the transition from BFU-E to CFU-E.

Reproductive development in two species of Darwinia Rudge (Myrtaceae)

1969 ◽  
Vol 17 (2) ◽  
pp. 215 ◽  
Author(s):  
N Prakash
Keyword(s):  
Embryo Sac ◽  
Pollen Grains ◽  
Reproductive Development ◽  
Outer Zone ◽  
Mature Embryo ◽  
Globular Embryo ◽  
Primary Endosperm Nucleus ◽  
Oil Glands ◽  
Polygonum Type ◽  
History Of

In Darwinia the floral parts are differentiated in a "calyx-orolla-gynoeciumandroecium" sequence. In individual buds stages of microsporogenesis markedly precede corresponding stages of megasporogenesis. The anther is tetrasporangiate with all sporangia lying in one plane. The secretory tapetum is one- to three-layered within the same microsporangium and a large number of Ubisch bodies are formed. The anthers dehisce by minute lateral pores and an ingenious mechanism helps disperse the twocelled pollen grains. A basal placenta in the single loculus of the ovary bears four ovules in D. micropetala and two in D. fascicularis. In both species, however, only one ovule is functional after fertilization. The fully grown ovules are anatropous, crassinucellar, and bitegmic; the inner integument forms the micropyle. The parietal tissue is most massive at the completion of megasporogenesis but is progressively destroyed later. The embryo sac follows the Polygonum type of developnlent and when mature is five-nucleate, the three antipodals being ephemeral. Following fertilization, the primary endosperm nucleus divides before the zygote. Subsequent nuclear divisions in the endosperm mother cell are synchronous and lead to a free-nuclear endosperm which becomes secondarily cellular, starting from the micropylar end at the time the globular embryo assumes an elongated shape. Embryogeny is irregular and the mature embryo is straight with a massive radicle and a hypocotyl which terminates in two barely recognizable cotyledons. Sometimes the minute cotyledons are borne on a narrow neck-like extension of the hypocotyl. A suspensor is absent. Both integuments are represented in the seed coat and only the outer layer of the outer and the inner layer of the inner integuments, with their thick-walled tanniniferous cells, remain in the fully grown seed. The ovary wall is demarcated into an outer zone containing oil glands surrounded by cells containing a tannin-like substance and an inner zone of spongy parenchyma. In the fruit this spongy zone breaks down completely but the outer zone is retained. The two species of Darwinia, while closely resembling each other in their embryology, differ significantly from other Myrtaceae. However, no taxonomic conclusions are drawn at this stage, pending enquiry into the life history of other members of the tribe Chamaelaucieae.

scholarly journals Exploiting the Binocular Head in Polarized Light Microscopy

1994 ◽  
Vol 2 (4) ◽  
pp. 16-16
Author(s):  
Walter C. McCrone
Keyword(s):  
Light Microscopy ◽  
Polarized Light ◽  
Polarized Light Microscopy ◽  
The Other ◽  
Monocular Viewing ◽  
Area Of Interest

Having been brought up on monocular microscopes I find the omnipresent binocular systems a luxury. To support this viewpoint I'd like to suggest some benefits you may not have considered.Because I'm used to monocular viewing I sometimes use two different oculars, say 10X and 25X, in order to scan quickly to find an area of interest and then to examine the detail with higher magnification. Occasionally I use both oculars simultaneously and “concentrate” on either image to the exclusion of the other. A better way is to set the interocular distance at the extreme setting most different from your own interocular distance. By moving your head about a centimeter either way you can use either ocular.

Micromere lineages in the glossiphoniid leechHelobdella

Development ◽  
2002 ◽  
Vol 129 (3) ◽  
pp. 719-732 ◽  
Author(s):  
Françoise Z. Huang ◽  
Dongmin Kang ◽  
Felipe-Andres Ramirez-Weber ◽  
Shirley T. Bissen ◽  
David A. Weisblat
Keyword(s):  
Early Development ◽  
Normal Development ◽  
The Other ◽  
Small Cells ◽  
Spiral Cleavage ◽  
Helobdella Robusta

In leech embryos, segmental mesoderm and ectoderm arise from teloblasts by lineages that are already relatively well characterized. Here, we present data concerning the early divisions and the definitive fate maps of the micromeres, a group of 25 small cells that arise during the modified spiral cleavage in leech (Helobdella robusta) and contribute to most of the nonsegmental tissues of the adult. Three noteworthy results of this work are as follows. (1) The c′′′ and dm′ clones (3d and 3c in traditional nomenclature) give rise to a hitherto undescribed network of fibers that run from one end of the embryo to the other. (2) The clones of micromeres b′′ and b′′′ (2b and 3b in traditional nomenclature) die in normal development; the b′′ clone can be rescued to assume the normal c′′ fate if micromere c′′ or its clone are ablated in early development. (3) Two qualitative differences in micromere fates are seen between H. robusta (Sacramento) and another Helobdella sp. (Galt). First, in Helobdella sp. (Galt), the clone of micromere b′′ does not normally die, and contributes a subset of the cells arising exclusively from c′′ in H. robusta (Sacramento). Second, in Helobdella sp. (Galt), micromere c′′′ makes no definitive contribution, whereas micromere dm′ gives rise to cells equivalent to those arising from c′′′ and dm′ in H. robusta (Sacramento).

scholarly journals Glomerulonephritis in schistosomiasis with mesangial IgM deposits

1981 ◽  
Vol 76 (2) ◽  
pp. 181-188 ◽  
Author(s):  
Ageu Godoy Magalhães Filho ◽  
Antônio Victoriano Barbosa ◽  
Teresa Cristina Ferreira
Keyword(s):  
Cell Proliferation ◽  
Light Microscopy ◽  
Immunofluorescence Microscopy ◽  
The Other ◽  
Proliferative Glomerulonephritis ◽  
Mesangial Proliferative Glomerulonephritis ◽  
Normal Pattern ◽  
Glomerular Lesions ◽  
Capillary Walls ◽  
Igm Deposits

Twenty one cases of hepatoesplenic schistosomiasis patients without clinical and laboratory evidence of renal disease, were studied by surgical biopsies using light microscopy and immunofluorescence. The cases were classified histologically as: normal pattern (6 cases); minimal changes (6 cases); and mesangial proliferative glomerulonephritis (9 cases). By the immunofluorescence microscopy using anti IgM, IgG, IgA and C3, the predominant finding in all biopsies, except the normal cases, was granular deposits of IgM in the mesangium along with C3. On the other hand, IgG was present in all cases including normal biopsies along the capillary walls. However IgG was also present in the mesangium only in cases with glomerular lesions. This finding may well be similar to that recently described as IgM mesangial nephropathy. According to our cases a mesangial proliferative glomerulonephritis, characterized by segmental cell proliferation and deposition of IgM in the mesangium, is probably the entity found in the early stages of mansonic schistosomiasis.

scholarly journals Demonstrating Pathogenicity of Enterobacter cloacae on Macadamia and Identifying Associated Volatiles of Gray Kernel of Macadamia in Hawaii

Plant Disease ◽  
2007 ◽  
Vol 91 (10) ◽  
pp. 1221-1228 ◽  
Author(s):  
K. A. Nishijima ◽  
M. M. Wall ◽  
M. S. Siderhurst
Keyword(s):  
Acetic Acid ◽  
Volatile Compounds ◽  
Enterobacter Cloacae ◽  
The Other ◽  
Biotic Factors ◽  
Macadamia Integrifolia ◽  
Abiotic And Biotic Factors ◽  
Foul Odor ◽  
Important Disease

Gray kernel is an important disease of macadamia (Macadamia integrifolia) that affects the quality of kernels, causing gray discoloration and a permeating, foul odor. Gray kernel symptoms were produced in raw, in-shell kernels of three cultivars of macadamia that were inoculated with strains of Enterobacter cloacae. Koch's postulates were fulfilled for three strains, demonstrating that E. cloacae is a causal agent of gray kernel. An inoculation protocol was developed to consistently reproduce gray kernel symptoms. Among the E. cloacae strains studied, macadamia strain LK 0802-3 and ginger strain B193-3 produced the highest incidences of disease (65 and 40%, respectively). The other macadamia strain, KN 04-2, produced gray kernel in 21.7% of inoculated nuts. Control treatments had 1.7% gray kernel symptoms. Some abiotic and biotic factors that affected incidence of gray kernel in inoculated kernels were identified. Volatiles of gray and nongray kernel samples also were analyzed. Ethanol and acetic acid were present in nongray and gray kernel samples, whereas volatiles from gray kernel samples included the additional compounds, 3-hydroxy-2-butanone (acetoin), 2,3-butanediol, phenol, and 2-methoxyphenol (guaiacol). This is believed to be the first report of the identification of volatile compounds associated with gray kernel.

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