Soybean and Bees
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Table 3. Seed <strong>and</strong> pod chronological development in soybean.<br />
Days after<br />
flowering<br />
Morphological <strong>and</strong> anatomical features<br />
0 Resting zygote. Several divisions of primary endosperm nucleus.<br />
1 Two-celled proembryo. Endosperm with about 20 free nuclei.<br />
2 Four- to eight-celled proembryo.<br />
3<br />
4-5<br />
Differentiation into proembryo proper <strong>and</strong> suspensor. Endosperm in peripheral layer<br />
with large central vacuole.<br />
Spherical embryo with protoderm <strong>and</strong> large suspensor. Endosperm surrounding<br />
embryo is cellular but elsewhere it is mostly acellular <strong>and</strong> vacuolated.<br />
6-7 Initiation of cotyledons. Endosperm mostly cellular.<br />
8-10<br />
10-14<br />
14-20<br />
20-30<br />
30-50<br />
Rotation of cotyledons begins. Procambium appears in cotyledons <strong>and</strong> embryo axis. All<br />
tissue systems of hypocotyl present. Root cap present over root initials. Endosperm all<br />
cellular.<br />
Cotyledons have finished rotation <strong>and</strong> are in normal position, with inner surfaces of<br />
cotyledons parallel with sides of ovules. Cotyledons elongate toward chalazal end of<br />
ovule. Primary leaf primordia present. Endosperm occupies about half of seed cavity.<br />
Extensive vascularization of seed coat.<br />
Continued growth of embryo <strong>and</strong> seed. Reduction of endosperm tissue by assimilation<br />
into cotyledons.<br />
Primary leaves reach full size. Primordium of first trifoliolate leaf present. Cotyledons<br />
reach maximum size. Endosperm almost gone.<br />
Continued accumulation of dry matter, <strong>and</strong> loss in fresh weight of seeds <strong>and</strong> pods.<br />
Maturation of pods.<br />
50-80 Maturity time<br />
Source: Carlson <strong>and</strong> Lester (1987). The times are a compilation of data from several soybean cultivars studied by Bils <strong>and</strong> Howell (1963), Carlson<br />
(1973), Fukui <strong>and</strong> Gotoh (1962), Meng-yuan (1963), Kamata (1952), Kato et al. (1954), Ozaki et al. (1956), Pamplin (1963), Suetsugu et al. (1962). The<br />
sequence is the same for modern cultivars, but times will vary according to genetic background, latitude, environmental conditions <strong>and</strong> presence/absence<br />
of biotic/abiotic stresses.