Fine structure of megagametophyte development in Zea mays

1979 ◽  
Vol 57 (10) ◽  
pp. 1093-1110 ◽  
Author(s):  
Scott D. Russell

Polygonum-type embryo sac development was examined in Zea mays with light, fluorescence, and electron microscopy. Megasporocyte polarity is expressed in organelle distribution, aniline blue wall fluorescence, and chalazal location of plasmodesmata. In the meiotic cytoplasm concurrent with the sporophyte–gametophyte transition, ribosome concentrations are low, and membrane-bound organelles are simplified. The functional megaspore is the largest and most chalazal cell of the resultant triad or tetrad. Aniline blue fluorescence is intense in nonfunctional megaspore walls, whereas in the functional megaspore intensity decreases from the chalazal end to that in nucellar walls. Throughout functional megaspore and two-nucleate megagametophyte, ribosome concentrations, organelle numbers, and structural complexity increase. The transition from vegetative to reproductive gametophytic growth presumably follows this biosynthetic period. In the four-nucleate stage, a second phase of mitochondrial simplification coincides with the formation of an extensive lytic vacuole containing evidence of possible organelle and cytoplasmic membrane incorporation. Near the close of intensive lytic activity, compartmentalization of lytic areas contributes to creating a prominent vacuole in the central cell as synergids, egg, and antipodals differentiate.


2004 ◽  
Vol 82 (11) ◽  
pp. 1566-1575 ◽  
Author(s):  
Cynthia M Ross ◽  
Michael J Sumner

Megasporogenesis, embryo sac development, and pollen tubes in Arceuthobium americanum Nutt. ex Engelm. were investigated with light, fluorescence, and electron microscopy. The orthotropous ovular structure of A. americanum lacked integuments and possessed a nucellus that was largely continuous with and indistinguishable from the placenta; we coined this structure the placental–nucellar complex (PNC). Two megasporocytes became evident in the tenuinucellate PNC by mid-April, and had undergone bisporic megasporogenesis by mid-May. The upper cell from each dyad (distal to the base of the PNC) became a functional megaspore, although only one would develop into a seven-celled embryo sac. Like typical angiosperm embryo sacs, that of A. americanum possessed an egg cell having the ultrastructure reflective of a quiescent cell, and lacked cellulosic and (or) hemicellulosic wall material between the egg apparatus and central cell. However, the egg apparatus arose at the lower embryo sac pole, not at the upper as expected for an orthotropous ovule. A hypothetical model for the development of Arceuthobium ovules is the ancestral fusion and subsequent reduction of two anatropous ovules to form two embryo sacs within the PNC, of which only one completes development. The synergids have no role in pollen tube guidance, as tubes could be seen below each functional megaspore prior to megagametogenesis.Key words: Arceuthobium, embryo sac, megasporogenesis, mistletoe, pollen tubes, ultrastructure.



2005 ◽  
Vol 83 (5) ◽  
pp. 459-466 ◽  
Author(s):  
Cynthia M Ross ◽  
Michael J Sumner

Post-fertilization changes in the seven-celled embryo sac of the parasitic angiosperm Arceuthobium americanum Nutt. ex Engelm. were investigated with light, fluorescence, and electron microscopy. Two embryo sacs, of which only one is fertilized, are found within the reduced ategmic ovule (the placental–nucellar complex). All cells of the fertilized embryo sac developed thickened cellulosic and (or) hemicellulosic bounding walls and, aside from the degenerative synergid, acquired ultrastructure reflective of metabolically active cells. The filiform apparatus became thickened in the persistent synergid, and a similar structure developed in the antipodals. Unlike the changes observed in the zygote and central cell, those in the persistent synergid and antipodals were unusual, as these cells regularly degenerate after fertilization in a typical angiosperm; therefore, in A. americanum, they likely play a role in providing nutrition to the zygote and (or) central cell. A pouch-like outgrowth (caecum) initiated from the central cell near the primary endosperm nucleus and, after vacuolar expansion and intercellular growth, reached the base of the placental–nucellar complex in three days. The observation of mitochondria clusters within the central cell, caecum, and adjacent placental–nucellar complex cells suggests the caecum functions in embryo sac expansion and haustorial nutrient absorption.Key words: Arceuthobium, caecum, cell walls, fertilized embryo sac, mistletoe, ultrastructure.



1989 ◽  
Vol 37 (6) ◽  
pp. 519 ◽  
Author(s):  
J Carapetian ◽  
EA Rupert

Development of safflower ovules and female gametophytes was compared in fertile and genetically sterile F2 and backcross segregants from the cross between 'US-10' and '57-147' genotypes. Fertile plants formed normal anatropous ovules with eight-nucleate embryo sacs, typical of the angiosperms. One week before anthesis, the eight-nucleate embryo sac is well developed and undergoes rapid elongation and expansion during the 24 h prior to anthesis, accompanied by a doubling in length of the florets. Sterile plants also formed normal ovules, but apparently with a delayed initiation of meiosis which was subsequently arrested at Metaphase I. Embryo sacs did not form in sterile florets except for rare observations of uninucleate embryo sacs which began to degenerate before anthesis. The integumentary tapetum which normally developed upon completion of meiosis in fertile plants, was well developed during Prophase I of megasporogenesis in sterile plants. This observation suggests that cell differentiation and development of this nutritive jacket is basically controlled by the age of the ovules rather than initiated by appearance of the functional megaspore. Failure of both female and male gametogenesis seems to result from interaction of three independently segregating genes.



1994 ◽  
Vol 49 (7-8) ◽  
pp. 447-452 ◽  
Author(s):  
Sabine Lüthje ◽  
José A. Gonzaléz-Reyes ◽  
Placido Navas ◽  
Olaf Döring ◽  
Michael Böttger

Modulation of plasma membrane-bound NADH:hexacyanoferrate III oxidoreductase activities by dicumarol and warfarin was investigated with plasma membrane vesicles of Zea mays L. (cv. Sil Anjou 18) roots, prepared by aqueous two phase partitioning. Vesicles were about 65% right-side out orientated as demonstrated by enzyme latency of vanadate sensitive ATPase activity. Dicumarol or warfarin, respectively, inhibited NADH:hexacyanoferrate III oxidoreductase activity in a concentration-dependent manner and inhibition could be reversed partially by addition of quinones



1993 ◽  
Vol 103 (2) ◽  
pp. 593-596 ◽  
Author(s):  
S. Luthje ◽  
O. Doring ◽  
D. GroBmann ◽  
M. Niecke ◽  
M. Bottger


Microbiology ◽  
2010 ◽  
Vol 156 (6) ◽  
pp. 1890-1899 ◽  
Author(s):  
Jörn Voss ◽  
Armin Ehrenreich ◽  
Wolfgang Liebl

The growth of Gluconobacter oxydans DSM 7145 on meso-erythritol is characterized by two stages: in the first stage, meso-erythritol is oxidized almost stoichiometrically to l-erythrulose according to the Bertrand–Hudson rule. The second phase is distinguished from the first phase by a global metabolic change from membrane-bound meso-erythritol oxidation to l-erythrulose assimilation with concomitant accumulation of acetic acid. The membrane-associated erythritol-oxidizing enzyme was found to be encoded by a gene homologous to sldA known from other species of acetic acid bacteria. Disruption of this gene in the genome of G. oxydans DSM 7145 revealed that the membrane-bound polyol dehydrogenase not only oxidizes meso-erythritol but also has a broader substrate spectrum which includes C3–C6 polyols and d-gluconate and supports growth on these substrates. Cultivation of G. oxydans DSM 7145 on different substrates indicated that expression of the polyol dehydrogenase was not regulated, implying that the production of biomass of G. oxydans to be used as whole-cell biocatalysts in the biotechnological conversion of meso-erythritol to l-erythrulose, which is used as a tanning agent in the cosmetics industry, can be conveniently carried out with glucose as the growth substrate.



1984 ◽  
Vol 69 (1) ◽  
pp. 127-135
Author(s):  
E.G. Williams ◽  
R.B. Knox ◽  
V. Kaul ◽  
J.L. Rouse

In Rhododendron spp. and Ledum groenlandicum a callose wall is laid down around the zygote in the first 2 days after fertilization. The periodic acid/Schiff-positive, aniline blue-fluorescence-positive callosic wall is initiated adjacent to the degenerating synergid, extends to cover the entire zygote surface, and remains visible during the initiation of embryogeny as the zygote elongates before the first proembryonal division. Unfertilized ovules show eventual callose deposition in the ovule wall cells during senescence in undeveloped abscising pistils, but show no development of callose within the embryo sac. Possible roles of a zygote special callose wall are discussed.



2020 ◽  
Vol 12 (19) ◽  
pp. 3184
Author(s):  
Nicolò Camarretta ◽  
Peter A. Harrison ◽  
Arko Lucieer ◽  
Brad M. Potts ◽  
Neil Davidson ◽  
...  

The use of unmanned aerial vehicles (UAVs) for remote sensing of natural environments has increased over the last decade. However, applications of this technology for high-throughput individual tree phenotyping in a quantitative genetic framework are rare. We here demonstrate a two-phased analytical pipeline that rapidly phenotypes and filters for genetic signals in traditional and novel tree productivity and architectural traits derived from ultra-dense light detection and ranging (LiDAR) point clouds. The goal of this study was rapidly phenotype individual trees to understand the genetic basis of ecologically and economically significant traits important for guiding the management of natural resources. Individual tree point clouds were acquired using UAV-LiDAR captured over a multi-provenance common-garden restoration field trial located in Tasmania, Australia, established using two eucalypt species (Eucalyptus pauciflora and Eucalyptus tenuiramis). Twenty-five tree productivity and architectural traits were calculated for each individual tree point cloud. The first phase of the analytical pipeline found significant species differences in 13 of the 25 derived traits, revealing key structural differences in productivity and crown architecture between species. The second phase investigated the within species variation in the same 25 structural traits. Significant provenance variation was detected for 20 structural traits in E. pauciflora and 10 in E. tenuiramis, with signals of divergent selection found for 11 and 7 traits, respectively, putatively driven by the home-site environment shaping the observed variation. Our results highlight the genetic-based diversity within and between species for traits important for forest structure, such as crown density and structural complexity. As species and provenances are being increasingly translocated across the landscape to mitigate the effects of rapid climate change, our results that were achieved through rapid phenotyping using UAV-LiDAR, raise the need to understand the functional value of productivity and architectural traits reflecting species and provenance differences in crown structure and the interplay they have on the dependent biotic communities.



2009 ◽  
Vol 61 (3) ◽  
pp. 831-841 ◽  
Author(s):  
Angela Mika ◽  
Marike Johanne Boenisch ◽  
David Hopff ◽  
Sabine Lüthje


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