Mr. Thorpe et al., CARBON IMPORT INTO DEVELOPING OVULES OF PISUM-SATIVUM - THE ROLE OF THE WATER RELATIONS OF THE SEED COAT, Journal of Experimental Botany, 44(262), 1993, pp. 937-945
We tested the hypothesis that the transport of carbon to developing pe
a ovules is controlled by the water potential of the seed coat, in bot
h the short-term (minutes to hours) and long-term (days). At 14 d afte
r anthesis, when the embryo just fills the seed coat, the osmotic pres
sure of seed coat apoplast solution was about 1 MPa (equivalent to 400
mOsmol kg-1). Transport of carbon into perfused attached seed coats a
t this stage of development was monitored with radioactive carbon-11.
After a small (50 mOsmol kg-1) increment in the osmotic pressure of th
e bathing solution, transport of carbon increased abruptly, but after
about 100 min it returned towards pretreatment values. Therefore, alth
ough osmotic pressure in the sink apoplast initially affected carbon i
mport, as expected from the Munch hypothesis, we concluded that it was
not a factor able to control import. At the same time, seed coat cell
turgor, measured with the pressure probe, initially decreased but res
umed pretreatment values within about 20 min, implying that turgor-reg
ulation in the sink maintained import despite the change of apoplastic
concentration. In the longer term, from 4 to 33 d after anthesis, bot
h the water potential and the inferred turgor of the cells of the seed
coat approached zero so that the driving force for influx increased,
although the rate of carbon influx was declining. Therefore, despite t
he importance for carbon inflow of turgor in sieve tubes in the sink,
the turgor of the entire tissue was not a factor which varied to contr
ol import via any direct effect on pressure gradients in the sieve tub
es.