scholarly journals Embryological Observations of Fruit Development in Mimosa pudica Linn.

2021 ◽  
Vol 4 (2) ◽  
pp. 130-132
Author(s):  
Yogesh Shastri

The present papers deal with embryological studies of the fruit development in Mimosa pudica Linn.. Observations on seed coat development is of exotestal pattern and is of multiplicative type, Pericarp is differentiated into epicarp, mesocarp and endocarp were noted.

Our Nature ◽  
1970 ◽  
Vol 7 (1) ◽  
pp. 177-181 ◽  
Author(s):  
B. Niroula ◽  
D. Parajuli ◽  
S. Jha

All the freshly collected mature seeds of M. pudica were greenish in colour, whereas 7 year old stored seeds were a mixture of greenish and brownish seeds. The greenish seeds had hard seed coat and acid treated as well as sand rubbing for 6-10 min greatly enhanced their germination percentage. The brownish seeds were simply the deteriorated form of greenish seeds. Leaves and pods had higher contribution to total plant dry weight in ungrazed field and in pot-cultured plants clipped a month before flowering. The young shoots of the plant had 18.9% crude protein, 0.46% phosphorus and 25.4% crude fibre on dry weight basis.Key words: Hard seed coat, Mimosa pudica, scarification, dry matter productionDOI: 10.3126/on.v7i1.2568Our Nature (2009) 7:177-181  


PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7996 ◽  
Author(s):  
Qikui Wu ◽  
Zihan Zhang ◽  
Huan Peng ◽  
Yali Wu ◽  
Fangyuan Yu

Background Styrax tonkinensis is a great potential biofuel as the species contains seeds with a particularly high oil content. Understanding the nutrient distribution in different parts of the fruit is imperative for the development and enhancement of S. tonkinensis as a biodiesel feedstock. Methods From 30 to 140 days after flowering (DAF), the development of S. tonkinensis fruit was tracked. The morphology change, nutrient content, and activity of associated enzymes in the continuum of the pericarp, seed coat, and kernel were analyzed. Results Between 30 and 70 DAF, the main locus of dry matter deposition shifted from the seed coat to the kernel. The water content within the pericarp remained high throughout development, but at the end (130 DAF later) decreased rapidly. The water content within both the seed coat and the kernel consistently declined over the course of the fruit development (30–110 DAF). Between 70 and 80 DAF, the deposition centers for sugar, starch, protein, potassium, and magnesium was transferred to the kernel from either the pericarp or the seed coat. The calcium deposition center was transferred first from pericarp to the seed coat and then to the kernel before it was returned to the pericarp. The sucrose to hexose ratio in the seed coat increased between 30 and 80 DAF, correlating with the accumulation of total soluble sugar, starch, and protein. In the pericarp, the sucrose to hexose ratio peaked at 40 and 100 DAF, correlating with the reserve deposition in the following 20–30 days. After 30 DAF, the chlorophyll concentration of both the pericarp and the seed coat dropped. The maternal unit (the pericarp and the seed coat) in fruit showed a significant positive linear relationship between chlorophyll b/a and the concentration of total soluble sugar. The potassium content had significant positive correlation with starch (ρ = 0.673, p = 0.0164), oil (ρ = 0.915, p = 0.000203), and protein content (ρ = 0.814, p = 0.00128), respectively. The concentration of magnesium had significant positive correlation with starch (ρ = 0.705, p = 0.0104), oil (ρ = 0.913, p = 0.000228), and protein content (ρ = 0.896, p = 0.0000786), respectively. Calcium content had a significant correlation with soluble sugar content (ρ = 0.585, p = 0.0457). Conclusions During the fruit development of S. tonkinensis, the maternal unit, that is, the pericarp and seed coat, may act a nutrient buffer storage area between the mother tree and the kernel. The stage of 70–80 DAF is an important time in the nutrient distribution in the continuum of the pericarp, seed coat, and kernel. Our results described the metabolic dynamics of the continuum of the pericarp, seed coat, and kernel and the contribution that a seed with high oil content offers to biofuel.


2020 ◽  
Author(s):  
Han-Yu Ko ◽  
Li-Hsuan Ho ◽  
H. Ekkehard Neuhaus ◽  
Woei-Jiun Guo

ABSTRACTTomato, an important fruit crop worldwide, requires efficient sugar allocation for fruit development. However, molecular mechanisms for sugar import to fruits remain poorly understood. Expression of SWEET (Sugars Will Eventually be Exported Transporters) proteins is closely linked with hexose ratio in tomato fruits and may be involved in sugar allocation. Here, using quantitative PCR, we discovered that SlSWEET15 was highly expressed in developing fruits compared to vegetative organs. Based on in situ hybridization and GUS fusion analyses, SlSWEET15 proteins accumulated in vascular tissues and seed coats, major sites of sucrose unloading in fruits. Localizing SlSWEET15-GFP to the plasma membrane supported its putative role in apoplasmic sucrose unloading. The sucrose transport activity of SlSWEET15 was confirmed by complementary growth assays in a yeast mutant. Elimination of the SlSWEET15 function by CRISPR/cas9 gene editing significantly decreased average sizes and weights of fruits, with severe defects in seed filling and embryo development. Together, we confirmed the role of SlSWEET15 in mediating sucrose efflux from the releasing phloem to the fruit apoplasm and subsequent import into parenchyma cells during fruit development. Furthermore, SlSWEET15-mediated sucrose efflux was also required for sucrose unloading from the seed coat to the developing embryo.One-sentence SummarySlSWEET15, a specific sucrose uniporter in tomato, mediates apoplasmic sucrose unloading from releasing phloem cells and seed coat for carbon supply during fruit expansion and seed filling.


Author(s):  
R. W. Yaklich ◽  
E. L. Vigil ◽  
W. P. Wergin

The legume seed coat is the site of sucrose unloading and the metabolism of imported ureides and synthesis of amino acids for the developing embryo. The cell types directly responsible for these functions in the seed coat are not known. We recently described a convex layer of tissue on the inside surface of the soybean (Glycine max L. Merr.) seed coat that was termed “antipit” because it was in direct opposition to the concave pit on the abaxial surface of the cotyledon. Cone cells of the antipit contained numerous hypertrophied Golgi apparatus and laminated rough endoplasmic reticulum common to actively secreting cells. The initial report by Dzikowski (1936) described the morphology of the pit and antipit in G. max and found these structures in only 68 of the 169 seed accessions examined.


1992 ◽  
Vol 85 (1) ◽  
pp. 69-76 ◽  
Author(s):  
Maria-Jose Sanchez-Beltran ◽  
Juan Carbonell ◽  
Jose L. Garcia-Martinez ◽  
Isabel Lopez-Diaz

Fruits ◽  
2015 ◽  
Vol 70 (4) ◽  
pp. 201-212 ◽  
Author(s):  
Esther Aurora Ruiz Huerta ◽  
Judith Márquez Guzmán ◽  
Clara Pelayo Zaldívar ◽  
Claudia Barbosa Martínez ◽  
Leticia Ponce de León García

2020 ◽  
Vol 45 (3) ◽  
pp. 478-482
Author(s):  
Steven R. Manchester

Abstract—The type material on which the fossil genus name Ampelocissites was established in 1929 has been reexamined with the aid of X-ray micro-computed tomography (μ-CT) scanning and compared with seeds of extant taxa to assess the relationships of these fossils within the grape family, Vitaceae. The specimens were collected from a sandstone of late Paleocene or early Eocene age. Although originally inferred by Berry to be intermediate in morphology between Ampelocissus and Vitis, the newly revealed details of seed morphology indicate that these seeds represent instead the Ampelopsis clade. Digital cross sections show that the seed coat maintains its thickness over the external surfaces, but diminishes quickly in the ventral infolds. This feature, along with the elliptical chalaza and lack of an apical groove, indicate that Ampelocissites lytlensis Berry probably represents Ampelopsis or Nekemias (rather than Ampelocissus or Vitis) and that the generic name Ampelocissites may be useful for fossil seeds with morphology consistent with the Ampelopsis clade that lack sufficient characters to specify placement within one of these extant genera.


1997 ◽  
Vol 66 (2) ◽  
pp. 253-259 ◽  
Author(s):  
Shiping Wang ◽  
Goro Okamoto ◽  
Ken Hirano

2005 ◽  
Vol 16 (3) ◽  
pp. 249-254
Author(s):  
Tomoko Kimura ◽  
Mieko Kagaya ◽  
Michitaka Naitou ◽  
Hiroko Sasaki ◽  
Tatsuyuki Sugahara

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