scholarly journals Les plastides et le chondriome pendant la gonogenèse dans le Gagea lutea L.

2017 ◽  
Vol 4 (1) ◽  
pp. 77-86 ◽  
Author(s):  
Stefan Krupko
Keyword(s):  
2016 ◽  
Vol 1 ◽  
pp. 34-39
Author(s):  
Victoria Gnjezdilova ◽  
Oksana Nespljak ◽  
Vira Bunjak ◽  
Ljubov Makhovska

Abstract. In the article were presented the results of studying the early spring synusias in the forests of Fageto-Carpineto-Querceta roboris subformation on the Pricarpathian territory. In the studied subformation were separated five associations: Fageto-Carpineto-Quercetum roboris galiosum odorati, Fageto-Carpineto-Quercetum roboris caricetum pilosae, Fageto-Carpineto-Quercetum roboris vincosum, Fageto-Carpineto-Quercetum roboris galeobdolosum, Fageto-Carpineto-Quercetum roboris hederosum. The revealed early spring synusias are formed by the following herbal species: Leucojum vernum L. (Amaryllidacea), Galanthus nivalis L. (Amaryllidacea), Dentaria glandulosa Waldst. et Kit. (Brassicaceae), Anemone nemorosa L.(Ranunculaceae), Scilla bifolia L. (Liliaceae), Isopyrum thalictroides L. (Ranunculaceae), Corydalis cava (L.) Schweigg. Koerte (Papaveraceae) та Gagea lutea (L.) Ker.-Gawl. (Liliaceae). It appears before the leaves blooming and forms the specific white-lilac-blue aspect. Galanthus nivalis L. synusias develops the first and then in the third decade of March develops the group with Anemone nemorosa L. domination. Last years as the result of the negative anthropogenic influence the number of Leucojum vernum L. and Galanthus nivalis L. groups – the rare ephemeroids put to the Ukrainian Red book was abruptly shortened.


2012 ◽  
Vol 59 (1) ◽  
pp. 83-90
Author(s):  
Ewa Szczuka ◽  
Bożena Pawlikowska-Pawlęga ◽  
Ewa Skórzyńska-Polit ◽  
Jolanta Sobieska ◽  
Jarosław Pawelec ◽  
...  

Localization of lipoxygenase (LOX) in the microspore of <i>Gagea lutea</i> (L.) Ker.-Gaw. was investigated with the immunogold labelling method. The enzyme was found in the cytoplasm, nucleus and sporoderm. The most intensive reaction was observed in the cytoplasm, where the immunogold particles were sometimes grouped into clusters of several or more and showed the highest density. The smallest amount of particles occured in the sporoderm. The role of lipoxygenase in the microspore is discussed.


1969 ◽  
Vol 23 ◽  
pp. 2559-2560 ◽  
Author(s):  
Arnulv Stabursvik ◽  
Gösta Pettersson ◽  
Tove Motzfeldt ◽  
D. Heinegård ◽  
Alexandru T. Balaban ◽  
...  
Keyword(s):  

2015 ◽  
Vol 56 (2) ◽  
pp. 79-90 ◽  
Author(s):  
Joanna Świerczyńska ◽  
Jerzy Bohdanowicz

Abstract The study used fluorescence microscopy to examine changes in cytoskeleton configuration during development of the embryo suspensor in Gagea lutea and to describe them in tandem with the development of the embryo proper. During the early phase of embryo suspensor development, tubulin and actin filaments were observed in the cytoplasm of the basal cell from the micropylar to the chalazal ends of the cell. Around the nucleus of the basal cell were clusters of numerous microtubules. These accumulations of tubulin arrays congregated near the nucleus surface; numerous bundles of microtubules radiated from the nucleus envelope. At this time, microfil-aments formed a delicate network in the cytoplasm of the basal cell. In the fully differentiated embryo suspensor, microtubules were observed at the chalazal end of the basal cell. Numerous bundles of microtubules were visualized in the cytoplasm adjacent to the wall separating the basal cell from the embryo proper. Microfilaments formed a dense network which uniformly filled the basal cell cytoplasm. There were some foci of F-actin material in the vicinity of the nucleus surface and at the chalazal end of the basal cell. In all studied phases of embryo suspensor development a prominent cortical network of actin and tubulin skeleton was observed in embryo proper cells.


2012 ◽  
Vol 59 (1) ◽  
pp. 71-82 ◽  
Author(s):  
Ewa Szczuka ◽  
Jerzy Bohdanowicz ◽  
Joanna Świerczyńska ◽  
Jolanta Sobieska ◽  
Jacek Pietrusiewicz

The meiotic division of microsporocytes and pollen grain development in <i>Gagea lutea</i> (L.) Ker.-Gaw. (Liliaceae) with fluorescence microscope (excitation light 400 nm) was observed after squashing the anthers in DAPI solution (fluorochrom dying DNA). Up to 70% of microsporocytes and pollen grains during the microsporogenesis and pollen grain development take a regular course. In the remaining microsporocytes and pollen grains (30%) the disturbances in course of both processes were observed. The most often observed disturbances are "late" chromosomes and a presence of micronuclei. The divisions of microsporocytes in the anther loculi show a big asynchrony, which, like the disturbances during the course of microsporogenesis and pollen grain development, may be caused by the external factors. The microsporogenesis takes place during autumn and winter months: the pollen grains develop in winter. At this time the dividing microsporocytes and developing pollen grains are under the influence of abiotic factors as low temperature and a lack of water. These factors disturb the formation of microtubular cytoskeleton of the dividing microsporocytes and pollen grains, which causes the formation of sterile pollen grains.


Planta ◽  
1998 ◽  
Vol 204 (4) ◽  
pp. 506-514 ◽  
Author(s):  
Jiří Bu ◽  
Irma Ebert ◽  
Monica Ruffini-Castiglione ◽  
Jiří Široký ◽  
Boris Vyskot ◽  
...  

2004 ◽  
Vol 14 (4) ◽  
pp. 371-378 ◽  
Author(s):  
T. Kondo ◽  
T. Miura ◽  
N. Okubo ◽  
M. Shimada ◽  
C. Baskin ◽  
...  

The effects of temperature on embryo growth, radicle emergence and cotyledon emergence of Gagea lutea (Liliaceae), a perennial herb widely distributed in Europe, eastern Siberia, the Kurile Islands, Sakhalin and the Far East, were monitored outdoors and in laboratory tests. In Japan, this species inhabits open secondary grasslands and deciduous forests. Seeds with an underdeveloped embryo are dispersed in late May/early June in Hokkaido. The embryo elongates in autumn, and the radicle emerges from the seed in mid-October to mid-November, at temperatures of about 15/4°C. However, cotyledons do not emerge until April, after seeds with an emerged radicle are covered with snow (near 0°C) for about 4 months. In laboratory experiments, temperatures of 25/15°C or 20/10°C followed by 5–10°C were required for embryo growth and radicle emergence. Rate and percentage of cotyledon emergence were promoted by keeping seeds with an emerged radicle under snow. The optimum temperature for cotyledon emergence after 81 d under snow was 15/5°C. Thus, G. lutea has deep simple epicotyl morphophysiological dormancy, and this is the first report of epicotyl dormancy in the genus.


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