Ovular secretions in the micropylar canal of larches (Larix kaempferi and L. x eurolepis)

1999 ◽  
Vol 77 (4) ◽  
pp. 531-536 ◽  
Author(s):  
Patrick von Aderkas ◽  
Cathy Leary
Keyword(s):  
Central Cell ◽  
Larix Kaempferi ◽  
Ovule Development ◽  
Maximum Volume ◽  
Drop Volume ◽  
Cell Stage ◽  
Micropylar Canal

In Larix kaempferi (Lamb.) Carr. and L. × eurolepis A. Henry, a secretion fills the micropylar canal of the ovule during a period of archegonial development that ranges from central cell stage until fertilization. Dissection of the ovuliferous scales caused excess fluid to be exuded from the micropylar canal, forming a drop at the tip of the micropyle. This drop was collected, and its production was quantified. Drop volume was recorded, and the percentage of ovules with drops was counted. The maximum volume of 217 nL far exceeded the volume of the micropyle, which ranged between 18 ± 8 and 28 ± 7 nL (mean ± SD). Removal of drops resulted in further drops being secreted. No drops were produced in ovules that had aborted megagametophyte development.Key words: Larix, micropylar secretions, ovule development.

scholarly journals Spatio-Temporal Distribution of Cell Wall Components in the Placentas, Ovules and Female Gametophytes of Utricularia during Pollination

2021 ◽  
Vol 22 (11) ◽  
pp. 5622
Author(s):  
Bartosz Jan Płachno ◽  
Małgorzata Kapusta ◽  
Piotr Świątek ◽  
Krzysztof Banaś ◽  
Vitor F. O. Miranda ◽  
...  
Keyword(s):  
Pollen Tube ◽  
Female Gametophyte ◽  
Embryo Sac ◽  
Temporal Distribution ◽  
Arabinogalactan Proteins ◽  
Central Cell ◽  
Nutritive Tissue ◽  
Pollen Tube Guidance ◽  
Micropylar Canal

In most angiosperms, the female gametophyte is hidden in the mother tissues and the pollen tube enters the ovule via a micropylar canal. The mother tissues play an essential role in the pollen tube guidance. However, in Utricularia, the female gametophyte surpasses the entire micropylar canal and extends beyond the limit of the integument. The female gametophyte then invades the placenta and a part of the central cell has direct contact with the ovary chamber. To date, information about the role of the placenta and integument in pollen tube guidance in Utricularia, which have extra-ovular female gametophytes, has been lacking. The aim of this study was to evaluate the role of the placenta, central cell and integument in pollen tube pollen tube guidance in Utricularia nelumbifolia Gardner and Utricularia humboldtii R.H. Schomb. by studying the production of arabinogalactan proteins. It was also determined whether the production of the arabinogalactan proteins is dependent on pollination in Utricularia. In both of the examined species, arabinogalactan proteins (AGPs) were observed in the placenta (epidermis and nutritive tissue), ovule (integument, chalaza), and female gametophyte of both pollinated and unpollinated flowers, which means that the production of AGPs is independent of pollination; however, the production of some AGPs was lower after fertilization. There were some differences in the production of AGPs between the examined species. The occurrence of AGPs in the placental epidermis and nutritive tissue suggests that they function as an obturator. The production of some AGPs in the ovular tissues (nucellus, integument) was independent of the presence of a mature embryo sac.

Ovular secretions in the micropylar canal of larches (Larix kaempferi and L. x eurolepis)

1999 ◽  
Vol 77 (4) ◽  
pp. 531-536 ◽  
Author(s):  
Patrick von Aderkas ◽  
Cathy Leary
Keyword(s):  
Larix Kaempferi ◽  
Micropylar Canal

Sexual reproduction of Pinus contorta. I. Pollen development, the pollination mechanism, and early ovule development

1981 ◽  
Vol 59 (10) ◽  
pp. 1828-1843 ◽  
Author(s):  
John N. Owens ◽  
Sheila J. Simpson ◽  
Marje Molder
Keyword(s):  
Pollen Development ◽  
Pinus Contorta ◽  
Distal Part ◽  
Nuclear Division ◽  
Reproductive Potential ◽  
Ovule Development ◽  
Open Pollination ◽  
Micropylar Canal ◽  
Germinating Pollen ◽  
Female Gametophyte Development

Details of development and the phenology of postdormancy cone-bud development, microsporogenesis, pollen development, and pollination were similar for Pinus contorta var. contorta and var. latifolia growing near Victoria, B.C., but comparable stages of development for var. latifolia occurred about 1 month later near Prince George, B.C. Several developmental aspects were found which affect the reproductive potential of the species. Only 25% of the ovuliferous scales, mostly in the distal part of the cone, bear fertile ovules. Secretions formed on the ovules and micropylar arms which caused pollen to adhere to these surfaces. Pollination is by means of pollination drops which began to be exuded from the ovules about 2 weeks after the conelets began to emerge from their bud scales. Pollination drops were present within each conelet for 2 to 4 days. At that time conelets were most widely open. Pollination drops were then withdrawn as ovuliferous scales enlarged and sealed the conelets. Pollination drop exudation and withdrawal were affected by humidity and water stress within the tree. Cells lining the micropylar canal enlarged and sealed the micropyle after the conelet closed. Pollen settled into a pollen chamber in the nucellus tip where it germinated about 2 months after pollination. Ovules lacking germinating pollen aborted after megasporogenesis and before free nuclear division began. If many ovules aborted within a conelet, the conelet aborted before winter dormancy. Ovules began free nuclear female gametophyte development and pollen tubes extended into the nucellus before conelets stopped developing in mid-August.

Human Adenovirus Uptake by Preirnplantation Mouse Embryos

1972 ◽  
Vol 30 ◽  
pp. 268-269
Author(s):  
D. G. Chase ◽  
W. Winters ◽  
L. Piko
Keyword(s):  
Hela Cells ◽  
Human Adenovirus ◽  
Mouse Embryos ◽  
Equilibrium Density ◽  
Cell Stage ◽  
Virus Attachment ◽  
Preimplantation Mouse Embryos ◽  
Embryo Culture Medium ◽  
Preimplantation Mouse ◽  
Mouse Cells

Although the outlines of human adenovirus entry and uncoating in HeLa cells has been clarified in recent electron microscope studies, several details remain unclear or controversial. Furthermore, morphological features of early interactions of human adenovirus with non-permissive mouse cells have not been extensively documented. In the course of studies on the effects of human adenoviruses type 5 (AD-5) and type 12 on cultured preimplantation mouse embryos we have examined virus attachment, entry and uncoating. Here we present the ultrastructural findings for AD-5.AD-5 was grown in HeLa cells and purified by successive velocity gradient and equilibrium density gradient centrifugations in CsCl. After dialysis against PBS, virus was sedimented and resuspended in embryo culture medium. Embryos were placed in culture at the 2-cell stage in Brinster's medium.

Cell-matrix interactions in the early mouse embryo

1992 ◽  
Vol 50 (1) ◽  
pp. 600-601
Author(s):  
A.E. Sutherland ◽  
P.G. Calarco ◽  
C.H. Damsky
Keyword(s):  
Mouse Embryo ◽  
Giant Cells ◽  
Blastocyst Stage ◽  
Integrin Subunit ◽  
Β1 Integrin ◽  
Cell Stage ◽  
Early Mouse Embryo ◽  
Migratory Activity ◽  
Early Mouse ◽  
Cell Matrix Interactions

Cell-extracellular matrix (ECM) interactions mediated by the integrin family of receptors are critical for morphogenesis and may also play a regulatory role in differentiation during early development. We have examined the onset of expression of individual integrin subunit proteins in the early mouse embryo, and their roles in early morphogenetic events. As detected by immunoprecipitation, the α6, αV, β1, and β3 subunits are detected as early as the 4-cell stage, α5 at the hatched blastocyst stage and αl and α3 following blastocyst attachment. We tested the role of these integrins in the attachment and migratory activity of two cell populations of the early mouse embryo: the trophoblast giant cells, which invade the uterine stroma and ultimately contribute to the chorio-allantoic placenta, and the parietal endoderm, which migrates over the inner surface of the trophoblast and ultimately forms Reichert's membrane and the parietal yolk sac. Experiments were done in serum-free medium on substrates coated with laminin (Ln) and fibronectin (Fn). Trophoblast outgrowth occurs on Ln and its E8 fragment (long arm), but not on the E1’ fragment (cross region) (Figs. 1, 2 ). This outgrowth is inhibited by anti-E8, anti-Ln, and by the anti-β1 family antiserum anti-ECMR, but not by anti-αV or the function-perturbing GoH3 antibody that recognizes the α6/β1 integrin, a major Ln (E8) receptor. This suggests that trophoblast outgrowth on Ln or E8 is mediated by a different β1 integrin such as α3/β1. Early stages of trophoblast outgrowth (up to 48 hours) on Fn are inhibited by anti-Fn and by function-perturbing anti-αV antibodies, whereas at later times outgrowth becomes insensitive to anti-αV but remains sensitive to the anti-β1 family antiserum anti-ECMr, indicating that trophoblast cells modulate their interaction with Fn during outgrowth. Trophoblast outgrowth on vitronectin (Vn) is sensitive to anti-αV antibodies throughout the 5-day period examined.

Elemental Analysis of Phloem Tissue in Lemna Minor Root Tips

1980 ◽  
Vol 38 ◽  
pp. 798-799
Author(s):  
Patrick Echlin ◽  
Thomas Hayes ◽  
Clifford Lai ◽  
Greg Hook
Keyword(s):  
Vascular Tissue ◽  
Lemna Minor ◽  
Atomic Weight ◽  
Companion Cell ◽  
Root Tips ◽  
Phloem Tissue ◽  
Cell Stage ◽  
Phloem Parenchyma ◽  
Parenchyma Cells ◽  
Xylem Element

Studies (1—4) have shown that it is possible to distinguish different stages of phloem tissue differentiation in the developing roots of Lemna minor by examination in the transmission, scanning, and optical microscopes. A disorganized meristem, immediately behind the root-cap, gives rise to the vascular tissue, which consists of single central xylem element surrounded by a ring of phloem parenchyma cells. This ring of cells is first seen at the 4-5 cell stage, but increases to as many as 11 cells by repeated radial anticlinal divisions. At some point, usually at or shortly after the 8 cell stage, two phloem parenchyma cells located opposite each other on the ring of cells, undergo an unsynchronized, periclinal division to give rise to the sieve element and companion cell. Because of the limited number of cells involved, this developmental sequence offers a relatively simple system in which some of the factors underlying cell division and differentiation may be investigated, including the distribution of diffusible low atomic weight elements within individual cells of the phloem tissue.

Dependence of ovary growth on ovule development in Cucumis sativus

1990 ◽  
Vol 80 (1) ◽  
pp. 43-50 ◽  
Author(s):  
A. Varga ◽  
J. Bruinsma
Keyword(s):  
Cucumis Sativus ◽  
Ovule Development ◽  
Ovary Growth

Estimation of Carbon Stock and Uptake for Larix kaempferi Lamb.

2016 ◽  
Vol 7 (4) ◽  
pp. 499 ◽  
Author(s):  
Jin-Taek Kang ◽  
Yeong-Mo Son ◽  
Jong-Su Yim ◽  
Ju-Hyeon Jeon
Keyword(s):  
Carbon Stock ◽  
Larix Kaempferi
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