Table 3.
Microchannel radius (nm) | PredictedeRv per microchannel (× 104 nm3 s−1) | Microchannel numbers supporting observed Rv (× 104)f | Microchannel numbers per pdg | Pd numbers supporting observed Rv (× 103)h |
---|---|---|---|---|
0.5 | 2.46 | 472,313 | 33 | 143,125 |
1.0 | 39.3 | 29,524 | 17 | 17,367 |
1.5 | 199 | 5832 | 11 | 5302 |
2.0 | 629 | 1845 | 8 | 2306 |
4.0 | 10,057 | 115 | 4 | 288 |
8.0 | 160,916 | 7 | 2 | 35.0 |
10.0 | 392,900 | 3 | 1 | 10.0 |
Plasmodesmal number estimates are compared with an observed value for developing wheat grains at the SE/CC complex and vascular parenchyma cell interface of 44,000 × 103 per grain (Wang et al., 1995).
Estimates of microchannel radii of plasmodesmata (for details, see Section Is Symplasmic Sieve Element Unloading Dominated by Bulk Flow?)
Observed by volume flow rate (Rv) of 11.6 × 1013 nm3 s−1 (Fisher, 1990).
Averaged phloem sap viscosity of 2 × 10−9 MPa s (Mullendore et al., 2010).
Cell wall thickness and hence plasmodesmatal length between SE/CC complexes and vascular parenchyma cells in developing wheat grains—500 nm (Fisher and Cash-Clark, 2000a).
Rv predicted using the nominated data sets in the Hagen-Poiseuille Law (Equation 1).
Microchannel numbers supporting observed Rv derived as the ratio of observed by volume flowa to predicted flow rate per microchannele.
Microchannel numbers per plasmodesmata were estimated assuming that their equators (diameters) are positioned on a circumference of half the internal radius (i.e., 10.5 nm—Wang et al., 1995) of plasmodesmata interconnecting SE/CC complexes to vascular parenchyma cells and that they occupy 50% of this circumference.
Plasmodesmal numbers supporting the observed Rv derived as the ratio of microchannel numbers supporting observed Rfv and microchannel numbers per plasmodesmatag.