The GA–DELLA–OsMS188 module controls male reproductive development in rice

2021 ◽  
Author(s):  
Yue Jin ◽  
Xinyue Song ◽  
Huizhong Chang ◽  
Yueyue Zhao ◽  
Chenhao Cao ◽  
...  
HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 455f-456 ◽  
Author(s):  
D. Scott NeSmith ◽  
Gerard Krewer ◽  
Jeffrey G. Williamson

Crop vegetative and reproductive development are frequently divided into stages to describe progression of development. Such a description is useful in denoting developmental differences between cultivars, for making crop management decisions based on growth stages, and for clear communication among individuals concerned with research, management, and production of the crop. We have developed such a scale for leaf bud development in rabbiteye blueberry (Vaccinium ashei Reade). Our scale has six stages briefly described as follows: 1) dormant bud; 2) early green tip; 3) late green tip; 4) unfolding stage; 5) mouse-ear stage; 6) fully opened bud. Categorizing buds in this manner has proven useful in comparing rates of leaf development between cultivars and in response to winter chilling. The stages appear to be relevant to highbush blueberries (V. corymbosum) as well.


2018 ◽  
Vol 2 (suppl_1) ◽  
pp. S175-S179
Author(s):  
Maggie K Reynolds ◽  
Gwinyai E Chibisa ◽  
Amin Ahmadzadeh ◽  
John B Hall

1969 ◽  
Vol 17 (2) ◽  
pp. 215 ◽  
Author(s):  
N Prakash

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.


Botany ◽  
2015 ◽  
Vol 93 (5) ◽  
pp. 307-316 ◽  
Author(s):  
L.I. Lindström ◽  
L.F. Hernández

In sunflower (Helianthus annuus L.), there has been an intense genetic selection for achenes with agronomic value, such as greater mass, oil content, and disease resistance. However, the information regarding the anatomical events that control their growth and maturation is surprisingly scarce. The aim of the present work was to study sunflower male and female sporogenesis and gametogenesis, as well as cell division and enlargement and tissue differentiation in the ovary and the embryo, linking the timing of these events to two frequently used phenological scales and a thermal time scale. In addition, we propose an ontogenetic scale that integrates the results of the present work to that of previous studies on sunflower reproductive development. The unified scales presented here provide a framework for others to investigate the relationships uncovered in this study in different genetic backgrounds and under different growing conditions.


Apmis ◽  
2001 ◽  
Vol 109 (S103) ◽  
pp. S302-S319 ◽  
Author(s):  
L.E. Gray ◽  
J. Ostby ◽  
J. Furr ◽  
C.J. Wolf ◽  
C. Lambright ◽  
...  

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