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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell reports 18 (1998), S. 143-147 
    ISSN: 1432-203X
    Keywords: Key wordsNicotiana tabacum ; Male germ unit ; Scanning electron microscopy ; Sperm isolation ; Angiosperms
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Sperm cells are released from pollen tubes of tobacco as linked cells, associated with the vegetative nucleus in an assemblage known as the male germ unit (MGU). Using light microscopy, the MGU assemblage appears to be ensheathed by cytoplasmic material of the pollen tube, which may stabilize their association. Following their release, the shape of the sperm cells and vegetative nucleus changes from an ellipsoidal to a more spheroidal morphology. When most of the cytoplasmic material is dispersed, a boundary remains around the two sperm cells. Using scanning electron microscopy, the cytoplasmic material surrounding the MGU appears filamentous, sometimes twisted and rope-like. Based on these observations, the function of the MGU of tobacco is discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell reports 16 (1997), S. 555-560 
    ISSN: 1432-203X
    Keywords: Egg cell ; Nicotiana tabacum ; Sperm cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The isolation of male and female gametes is a precondition for the micromanipulation of flowering plant gametes. To reflect their condition at fertilization, isolated gametes need to be physiologically mature and vigorous. Sperm cells are isolated from pollen tubes grown on cut styles using the “in vivo/in vitro” technique. Embryo sacs are isolated 2 days after anthesis using brief treatments of minimal concentrations of cell-wall-digesting enzymes on ovules of emasculated flowers. Egg cells are then mechanically separated from the embryo sac, allowing unambiguous identification of cells. Two days is usually the minimum required for the pollen tube to penetrate the ovule and effect fertilization in vivo.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-203X
    Keywords: Key words In vitro fertilization ; Egg cell ; Nicotiana tabacum ; Polyethylene glycol ; Sperm cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract This research is part of an attempt to establish an in vitro fertilization system in tobacco to aid in understanding mechanisms of fertilization. Fusions of isolated male and female gametes were induced in a polyethylene glycol solution. Fusion appears similar to that in maize. One nuclear division of both an unfertilized egg cell and a synergid was induced in KM8p medium with 1 mg/l 2,4-dichlorophenoxyacetic acid in a microchamber culture; one cellular division of the egg cell was also induced in the same medium in solid-drop culture. The osmolality of suspension culture feeder cells was critical for the development of these cells. These results indicate that in vitro fertilization is possible in tobacco, which would be the first such system in dicots.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell reports 16 (1997), S. 555-560 
    ISSN: 1432-203X
    Keywords: Key words Egg cell ; Nicotiana tabacum ; Sperm cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The isolation of male and female gametes is a precondition for the micromanipulation of flowering plant gametes. To reflect their condition at fertilization, isolated gametes need to be physiologically mature and vigorous. Sperm cells are isolated from pollen tubes grown on cut styles using the ``in vivo/in vitro'' technique. Embryo sacs are isolated 2 days after anthesis using brief treatments of minimal concentrations of cell-wall-digesting enzymes on ovules of emasculated flowers. Egg cells are then mechanically separated from the embryo sac, allowing unambiguous identification of cells. Two days is usually the minimum required for the pollen tube to penetrate the ovule and effect fertilization in vivo.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-203X
    Keywords: In vitro fertilization ; Egg cell ; Nicotiana tabacum ; Polyethylene glycol ; Sperm cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract This research is part of an attempt to establish an in vitro fertilization system in tobacco to aid in understanding mechanisms of fertilization. Fusions of isolated male and female gametes were induced in a polyethylene glycol solution. Fusion appears similar to that in maize. One nuclear division of both an unfertilized egg cell and a synergid was induced in KM8p medium with 1 mg/l 2,4-dichlorophenoxyacetic acid in a microchamber culture; one cellular division of the egg cell was also induced in the same medium in solid-drop culture. The osmolality of suspension culture feeder cells was critical for the development of these cells. These results indicate that in vitro fertilization is possible in tobacco, which would be the first such system in dicots.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Sexual plant reproduction 13 (2000), S. 11-20 
    ISSN: 1432-2145
    Keywords: Key words Antimonate localization ; Calcium ; Embryo sac ; Ovule ; Plumbago zeylanica
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  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.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 208 (1999), S. 123-128 
    ISSN: 1615-6102
    Keywords: Immunogold ; Myosin ; Nicotiana tabacum ; Pollen tube ; Scanning electron microscopy ; Sperm cell transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Actomyosin interactions are reportedly the principal mechanism for the transport of nonmotile sperm cells of flowering plants inside the pollen tube and inside the embryo sac. Myosin has been demonstrated on the generative cell (the predecessor of sperm cells), although it is unclear from previous studies whether myosin is located directly on the plasma membrane of the male germ cells or on the external plasma membrane of the pollen cell that surrounds them. Immunogold scanning electron microscopy was used to localize myosin on isolated tobacco sperm cells, with and without associated membranes. When present, the pollen tube plasma membrane surrounding the sperm cells was labeled by an antimyosin antibody, as were pollen tube cytoplasmic organelles. Negligible labeling was observed directly on the plasma membrane of the sperm cells.
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  • 8
    Publication Date: 2009-09-01
    Print ISSN: 0006-3134
    Electronic ISSN: 1573-8264
    Topics: Biology
    Published by Springer
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  • 9
    Publication Date: 2011-12-01
    Print ISSN: 0006-3134
    Electronic ISSN: 1573-8264
    Topics: Biology
    Published by Springer
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  • 10
    Publication Date: 2010-07-13
    Description: The attribution of spatial and temporal variations in terrestrial methane (CH4) flux is essential for assessing and mitigating CH4 emission from terrestrial ecosystems. In this study, we used a process-based model, the Dynamic Land Ecosystem Model (DLEM), in conjunction with spatial data of six major environmental factors to attribute the spatial and temporal variations in the terrestrial methane (CH4) flux over North America from 1979 to 2008 to six individual factors and their interaction. Over the past three decades, our simulation indicates that global change factors accumulatively contributed 43.05 Tg CH4-C (1 Tg = 1012 g) emission over North America, among which ozone (O3) pollution led to a reduced CH4 emission by 2.69 Tg CH4-C, all other factors including climate variability, nitrogen (N) deposition, rising atmospheric carbon dioxide (CO2), N fertilization, and land conversion increased terrestrial CH4 emissions by 40.37 Tg CH4-C, 0.42 Tg CH4-C, 6.95 Tg CH4-C, 0.11 Tg CH4-C, and 3.70 Tg CH4-C, respectively, and interaction between/among these global change factors led to a decline of CH4 emission by 5.80 Tg CH4-C. Climatic variability dominated the inter-annual variations in terrestrial CH4 fluxes at both continental and country levels. The relative importance of each environmental factor in determining the magnitude of methane flux shows substantially spatial variation across North America. This factorial attribution of CH4 fluxes over the North America might benefit policy makers who would like to curb climate warming by reducing CH4 emission.
    Print ISSN: 1810-6277
    Electronic ISSN: 1810-6285
    Topics: Biology , Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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