Embryo sac development in some representatives of the tribe Cynodonteae (Poaceae)

Bothalia ◽  
1994 ◽  
Vol 24 (1) ◽  
pp. 101-105 ◽  
Author(s):  
A. Strydom ◽  
J. J. Spies
Keyword(s):  
Cynodon Dactylon ◽  
Embryo Sac ◽  
Polygonum Type ◽  
Embryo Sac Development ◽  
Obligate Apomixis ◽  
Chloris Virgata

Chloris virgata Sw., Cynodon dactylon (L.) Pers., Harpochloa falx (L. f.) Kuntze, and Tragus berteronianus Schult. have a Polygonum type of embryo sac development. Unreduced embryo sacs were found in Eustachys paspaloides (Vahl) Lanza Mattei,  Harpochloa falx, and  Rendlia altera (Rendle) Chiov. Both facultative and obligate apomixis were observed. The Hieracium type of embryo sac development was observed in the aposporic specimens.

Embryo sac development in some South African cultivars of Lantana camara

Bothalia ◽  
1982 ◽  
Vol 14 (1) ◽  
pp. 113-117 ◽  
Author(s):  
J. J. Spies ◽  
C. H. Stirton
Keyword(s):  
South Africa ◽  
South African ◽  
Embryo Sac ◽  
Lantana Camara ◽  
Polygonum Type ◽  
Definite Evidence ◽  
Embryo Sac Development ◽  
Antipodal Cells

Twenty embryo sacs from each of 20 different  Lantana camara L. cultivars naturalized in South Africa were examined. The normal sexual embryo sacs were monosporic 8-nucleated embryo sacs of the polygonum type and were encountered in 55% of the material examined. Several deviations from this pattern were recorded. Occasionally one of the nuclei failed to develop into a synergid, resulting in three polar nuclei. Contrary to published information, the antipodal cells did not increase in size, nor was there an increase in the number of nuclei per cell. Although the occurrence of sexuality is confirmed, no definite evidence exists for the occurrence of apomixis. The occurrence of two embryo sacs per locule might be the result of either apospory or of sexuality whereby two embryo sacs were formed from two megaspores.

Embryo sac and early ovule development in Oryzopsis miliacea and Stipa tortilis

1970 ◽  
Vol 48 (1) ◽  
pp. 27-41 ◽  
Author(s):  
Jack Maze ◽  
Lesly R. Bohm ◽  
Lyle E. Mehlenbacher Jr.
Keyword(s):  
Cell Division ◽  
Pollen Tube ◽  
Nuclear Division ◽  
Outer Integument ◽  
Embryo Sac ◽  
Ovule Development ◽  
Polygonum Type ◽  
Embryo Sac Development

The ovules of Stipa tortilis and Oryzopsis miliacea are hemianatropous, bitegmetic, and pseudocrassinucellate (sensu Davis 1966). The hemianatropous shape of the ovule is the result of characteristic patterns of cell division and enlargement in the chalazal area and areas alongside the embryo sac. Embryo sac development in both is Polygonum-type and both have proliferating antipodals. Endosperm is nuclear, although in O. miliacea it is atypical in that nuclear division is synchronous within one portion of the embryo sac, e.g. micropylar, but not synchronous between different portions of the embryo sac, e.g., micropylar and chalazal. Differences in ovule initiation, persistence of the outer integument, fate of the inner integument, nature of the nucellus, shape of the embryo sac, nature of the synergids, cytoplasm of the egg, polar nuclei, and endosperm exist between these two taxa. Both synergids of O. miliacea undergo changes before fertilization and one degenerates before fertilization. The pollen tube enters the embryo sac at the base of the persistent synergid. There is presently insufficient embryological data to permit meaningful speculation on relationships between Stipa and Oryzopsis. Embryologically, Stipa and Oryzopsis are festucoid grasses, as much other evidence indicates. Embryo sac development in the Gramineae is more similar to that of the Restionaceae than to that of the Cyperaceae. This is in contradiction to recent speculations on the relationships of the Gramineae.

Embryo sac and early embryo development in the salmonberry (Rubus spectabilis)

1969 ◽  
Vol 47 (12) ◽  
pp. 1891-1893 ◽  
Author(s):  
B. V. Virdi ◽  
G. W. Eaton
Keyword(s):  
Embryo Development ◽  
Diploid Species ◽  
Embryo Sac ◽  
Early Embryo ◽  
Polygonum Type ◽  
Early Embryo Development ◽  
Embryo Sac Development ◽  
Parent Clone

Embryo sac development was studied in two clones of salmonberry. U.B.C. clones I-37 and II-4 were used in the study. Clone II-4 is a ruby-fruited seedling of a gold-fruited parent. Clone I-37 is the gold-fruited seedling of a ruby-fruited parent. Reproduction was sexual and embryo development normal in this diploid species. Embryo sac development was of the normal or Polygonum type and abnormalities such as multiple embryo sacs and abbreviated integument were also found. Very generally, the development of embryo sacs in both clones was similar.

Embryology of Polygonatum (Asparagaceae) and its systematic significance

Phytotaxa ◽  
2018 ◽  
Vol 350 (3) ◽  
pp. 235
Author(s):  
YUAN-YUAN SONG ◽  
YUN-YUN ZHAO ◽  
JIA-XI LIU
Keyword(s):  
Female Gametophyte ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Mature Pollen ◽  
Polygonum Type ◽  
Male And Female ◽  
Systematic Significance ◽  
Embryo Sac Development

In this study, we systematically studied the microsporogenesis, megasporogenesis, as well as development of male and female gametophyte of Polygonatum macropodum and P. sibiricum using the conventional paraffin sectioning technique. Our results showed that 1) microsporocytes cytokinesis is of the successive type; 2) microspore tetrads are tetragonal or tetrahedral; 3) mature pollen grains are two-celled or three-celled; 4) ovary is superior and trilocular, with axile placentas bearing 4–6 anatropous per locule; 5) ovules are anatropous, crassinucellate and bitegmic, with micropyle formed by the inner integument; 6) megaspore tetrads are linear or T-shaped; 7) embryo sac development is typically of Polygonum-type. The embryological features of Polygonatum support its inclusion of Asparagaceae in Asparagales.

scholarly journals Development of Female Gametophyte in Gladiolus italicus Miller (Iridaceae)

Caryologia ◽  
2021 ◽  
Vol 74 (3) ◽  
pp. 91-97
Author(s):  
Ciler Kartal ◽  
Nuran Ekici ◽  
Almina Kargacıoğlu ◽  
Hazal Nurcan Ağırman
Keyword(s):  
Light Microscopy ◽  
Female Gametophyte ◽  
Embryo Sac ◽  
Polygonum Type ◽  
Gametophyte Development ◽  
Embryo Sac Development ◽  
Secondary Nucleus ◽  
Microscopy Techniques ◽  
Female Gametophyte Development ◽  
First Time

In this study gynoecium, megasporogenesis, megagametogenesis and female gametophyte of Gladiolus italicus Miller were examined cytologically and histologically by using light microscopy techniques. Ovules of G. italicus are of anatropous, bitegmic and crassinucellate type. Embryo sac development is of monosporic Polygonum type. Polar nuclei fuse before fertilization to form a secondary nucleus near the antipodals. The female gametophyte development of G. italicus was investigated for the first time with this study.

Embryo sac development in some South African Lantana species (Verbenaceae)

Bothalia ◽  
1984 ◽  
Vol 15 (1/2) ◽  
pp. 161-166 ◽  
Author(s):  
J. J. Spies
Keyword(s):  
South African ◽  
Embryo Sac ◽  
Lantana Camara ◽  
The South ◽  
Polygonum Type ◽  
Embryo Sac Development ◽  
Chalazal Megaspore

Evidence that the South African Lantana camara L. complex only produces sexual embryo sacs is provided. It is shown that the archesporium occasionally divides mitotically and that both archesporia form tetrads. The chalazal megaspore of one tetrad and the micropylar megaspore of the second tetrad develop into Polygonum type embryo sacs. L. rugosa Thunb. also forms Polygonum type embryo sacs. The L. rugosa embryo sac has a much more densely packed cytoplasm, smaller vacuole and the position of the polar nuclei differs from that of the L. camara embryo sac. It is possible to distinguish between  L. camara and  L. rugosa on their embryo sac morphology alone.

CONTRIBUTION TO THE EMBRYOLOGY OF HOPPEA DICHOTOMA WILLD. (GENTIANACEAE)

1961 ◽  
Vol 39 (5) ◽  
pp. 1001-1006 ◽  
Author(s):  
Govindappa D. Arekal
Keyword(s):  
Cell Wall ◽  
Female Gametophyte ◽  
Embryo Sac ◽  
Cell Wall Formation ◽  
Polygonum Type ◽  
Wall Formation ◽  
Embryo Sac Development ◽  
In Series ◽  
Second Period

The mode of embryo sac development in Hoppea dichotoma Willd. conforms to the Polygonum type. No integumentary tapetum is organized around the female gametophyte. The organization of the endosperm follows the nuclear type. Simultaneous cell wall formation occurs throughout the endosperm when the embryo is at the 4- to 6-celled stage. The development of the embryo is assigned to the second period, V megarchetype and group 11 in series C′ in the system of embryogenic classification of Souèges. The endosperm and embryo of Gentianaceae are compared with those of Menyanthaceae.

Ultrastructural Observation on Embryo Sac Development inPhaius tankervilliae(Aiton)Bl.

2012 ◽  
Vol 30 (2) ◽  
pp. 188 ◽  
Author(s):  
Dong-Mei LI ◽  
Cheng-Hou WU ◽  
Xiu-Lin YE ◽  
Cheng-Ye LIANG
Keyword(s):  
Embryo Sac ◽  
Ultrastructural Observation ◽  
Embryo Sac Development

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.

Embryological studies in the compositae, I. Sporogenesis, Gametogenesis, and Embryogeny in Cotula australis (Less.) Hook. F

1962 ◽  
Vol 10 (1) ◽  
pp. 1 ◽  
Author(s):  
GL Davis
Keyword(s):  
Mother Cell ◽  
Megaspore Mother Cell ◽  
Embryo Sac ◽  
Subsequent Development ◽  
Pollen Grains ◽  
Archesporial Cell ◽  
Polygonum Type ◽  
Wall Formation ◽  
Chalazal Megaspore

Cotula australis has a discoid heterogamous capitulum in which the outermost three whorls of florets are female and naked. The bisexual disk florets are fully fertile and have a four-lobed corolla with four shortly epipetalous stamens. The anthers contain only two microsporangia. Wall formation and microsporogenesis are described and the pollen grains are shed at the three-celled condition. The ovule is teguinucellate and the hypodermal archesporial cell develops directly as the megaspore mother cell. Megasporogenesis is normal and the monosporio embryo sac develops from the chalazal megaspore. Breakdown of the nucellar epidermis takes place when the embryo sac is binucleate and its subsequent development follows the Polygonum type. The synergids extend deeply into the micropyle and one persists until late in embryogeny as a haustorium. The development of the embryo is of the Asterad type, and the endosperm is cellular. C. coronopifolia agrees with C. australis in the presence of only two microsporangia in each anther and the development of a synergid haustorium.

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