According to Erbar (2003), there are numerous exudate-filled channels in the stigma <strong>and</strong> style, with pollen tubes growing in these channels, which provide nutrition <strong>and</strong> mechanical guidance. At the base of the stigma, in the transition zone between stigma <strong>and</strong> style, there is a gradual increase in the amount of exudate between cells, except in the center of the style. These cells comprise the stylar-transmitting tissue, secreting an exudate similar in appearance to that of the stigma. Pollen usually germinates on the surface of the film overlying the stigma exudate. Germination can also occur among the lower whorls of papillae, but these tubes then grow into the stigma before entering the style. Although many pollen grains are deposited on the stigma, <strong>and</strong> most of them germinate <strong>and</strong> grow into the stigma <strong>and</strong> upper style, the majority of the tubes atrophy <strong>and</strong> die before reaching the distal end of the ovary. Only a few pollen tubes reach the locule <strong>and</strong> compete for ovules to fertilize (Herrero <strong>and</strong> Hormaza, 1996). After germinating, pollen tubes grow between the cells of the stylar-transmitting tissue. The ovarian transmitting tissue forms a secretory obturator on top of which the pollen tubes grow toward the ovules (Erbar, 2003). Its exudate is pectinaceous, which perhaps controls the direction of pollen tube growth chemotactically (Cheung et al., 1995). During growth of the pollen tube toward the ovule, the generative cell divides <strong>and</strong> forms two male gametes, the sperm cells. Finally, the pollen tube grows through the micropyle of the ovule, between nucellar epidermal cells, <strong>and</strong> enters the filiform apparatus of the degenerate synergid. Here the pollen tube tip bursts <strong>and</strong> releases the two sperm cells. One sperm fuses with the egg <strong>and</strong> forms the diploid zygote, the first cell of the embryo, while the other sperm fuses with the secondary nuclei, forming the primary endosperm nucleus (Ray et al., 1997). Rustamova (1964) noted that the time from pollination to fertilization varies from about 8 to 10 h. Thus, the day of full opening of the flower is likely the very day of fertilization or, perhaps, is one day after fertilization. <strong>Soybean</strong>s are considered as cleistogamic, self-pollinating plants. The first studies indicated cross-pollination rate on soybeans to be as low as 0.04% in Wisconsin, with different varieties of soybean grown in adjacent rows, in different places (Woodworth, 1922), ranging from 0.70% <strong>and</strong> 0.18% in Virginia, in successive years (Garber <strong>and</strong> Odl<strong>and</strong>, 1926), <strong>and</strong> less than 1% in Iowa <strong>and</strong> Maryl<strong>and</strong> (Weber <strong>and</strong> Hanson, 1961). The cross pollination on soybeans is mediated by pollinators, especially the honeybee (Figure 19 <strong>and</strong> 20). 52 SoybeAn <strong>and</strong> bees
Figure 19. Apis mellifera visiting a soybean flower. Photo: Decio Luiz Gazzoni Photo: Decio Luiz Gazzoni Figure 20. Foraging bee covered by pollen grains. According to Ahrent <strong>and</strong> Caviness (1994), based on a 2-yr average, cross-pollination varied from a low of 0.09% for Walters cultivar to a high of 1.63% for ‘Brim’. The same authors mention that results show that cultivars differ significantly in the extent of cross-pollination <strong>and</strong> SoybeAn <strong>and</strong> bees 53
- Page 1 and 2: SOYBEAN and BEES Decio Luiz Gazzoni
- Page 3 and 4: Copies of this publication can be a
- Page 5: Photo: Paulo Robson de Souza This b
- Page 8 and 9: continuous development and use of p
- Page 11 and 12: PREFACE Soybeans (Glycine max (L.)
- Page 13 and 14: the pest abundance and the level of
- Page 15 and 16: Table of Contents Soybean cycle....
- Page 17 and 18: SOYBEAN cYCLE Soybean (Glycine max
- Page 19 and 20: es from pod set to physiological ma
- Page 21: Luckily for the growers - and for t
- Page 24 and 25: The tassel starts to develop inside
- Page 26 and 27: Flowers: Structure, anatomy and maj
- Page 28 and 29: ing region is the throat and the fl
- Page 30 and 31: Authors like Turck et al. (2008) as
- Page 32 and 33: In the microgametogenesis, the unic
- Page 34 and 35: dynamics, and the flux of ions are
- Page 36 and 37: Once confirmed, agricultural practi
- Page 39 and 40: Soybean reproductive development So
- Page 41 and 42: Photos: Decio Luiz Gazzoni A B Figu
- Page 43 and 44: Photo: Decio Luiz Gazzoni Photos: D
- Page 45 and 46: monecious or dioecious flowers. Fig
- Page 47 and 48: (Severson, 1983). He observed that
- Page 49 and 50: stage. However, in spite of its res
- Page 51: less prominent and quickly resemble
- Page 55 and 56: Embryo, endosperm and seed coat dev
- Page 57 and 58: Parallel to the embryo development
- Page 59 and 60: Bees and plants relations Nectar, a
- Page 61 and 62: with protection activity, as well a
- Page 63 and 64: mental tobacco are expressed in the
- Page 65 and 66: (2009) and its almost non-existence
- Page 67 and 68: guided to particular flowers by flo
- Page 69 and 70: crose, fructose, and glucose; domin
- Page 71 and 72: Nectar, aroma and fidelity of polli
- Page 73 and 74: Kram (2008) suggested a role in ant
- Page 75 and 76: in seeds, particularly at intermedi
- Page 77 and 78: legume nectaries. Species involved
- Page 79 and 80: cium. These bodies vary somewhat in
- Page 81: Trichomes and nectaries Gynoecium n
- Page 84 and 85: soybean flowers. Also, van der Lind
- Page 86 and 87: flowered varieties are inter-mixed
- Page 88 and 89: Table 5. Differences on yield compo
- Page 91 and 92: Pollinators foraging on soybeans Po
- Page 93: Erickson (1984) questioned whether
- Page 96 and 97: On the study of Chiari et al. (2013
- Page 98 and 99: al. (1983). Conversely, lower N and
- Page 100 and 101: the mean density did not reach the
- Page 102 and 103:
The golden rule for minimizing nega
- Page 104 and 105:
ALEXANDROVA, V. G.; ALEXANDROVA, O.
- Page 106 and 107:
BOLTEN, A. B.; FEINSINGER, P.; BAKE
- Page 108 and 109:
CARTER, C.; HEALY, R.; O´TOOL, N.
- Page 110 and 111:
CORBET, S. A.; DELFOSSE, E. Honeybe
- Page 112 and 113:
DZIKOWSKI, B. Studia nad soja Glyci
- Page 114 and 115:
FERRERES, F.; ANDRADE, P.; GIL, M.
- Page 116 and 117:
GALLAI, N.; SALLES, J. M.; SETTELE,
- Page 118 and 119:
GONZÁLEZ-TEUBER, M.; HEIL, M. The
- Page 120 and 121:
HEIL, M.; GONZÁLEZ-TEUBER, M.; CLE
- Page 122 and 123:
IVANOFF, S. S. KEITT, G. W. Relatio
- Page 124 and 125:
KLEIN, A. M.; STEFFAN-DEWENTER, I.;
- Page 126 and 127:
LINSKENS, H. F.; PFAHLER, P. L.; KN
- Page 128 and 129:
MOFFETT, J. O.; STITH, L. S. Honeyb
- Page 130 and 131:
PAMPLIN, R. A. The anatomical devel
- Page 132 and 133:
RADHIKA, V.; KOST, C.; BOLAND, W.;
- Page 134 and 135:
RUHLMANN, J. M.; KRAM, B. W.; CARTE
- Page 136 and 137:
TAKAHASHI, R.; MATSUMURA, H.; OYOO,
- Page 138 and 139:
VOGEL, S. Flowers offering fatty oi
- Page 140 and 141:
WIST, T. J.; DAVIS, A. R. Floral ne
- Page 143 and 144:
GLOSSARY Abaxial: Facing away from
- Page 145 and 146:
Megaspores: In angiosperms, one of
- Page 147 and 148:
Synergid: One of two small cells ly