The "source" level in the olive cultivar Leccino was varied by girdling at different stages of fruit growth. Afterwards, the effects on gas exchange, fruit growth, and ripening and blooming were studied. Girdling during fruit growth did not significantly influence net photosynthetic rate (PN) except in the last phase of fruit growth when the PN was reduced. In the girdled branch, PN began to decrease at the onset of starch accumulation because fruit growth ceased. In mid-November stomatal conductance (gs) and transpiration rate (E) were also reduced by girdling, whereas sub-stomatal CO2 concentration (Ci) increased in leaves from the girdled branches. The total chlorophyll content (Chl) tended to decrease in parallel with the reduced PN. Girdling did not substantially influence the leaf and shoot water contents. The large availability of assimilates seems to cause an earlier fruit ripening. In general, girdling increased fruit dry mass. Healing before the time when the majority of pulp growth occurs reduced the effect of girdling. June girdling increased the pit dry mass. Girdling at the beginning of August and September, compared to the control, increased the pulp dry mass, but the pit dry mass did not differ with respect to the control. The percentage of oil in the fruit, on a dry mass basis, increased with August and September girdlings, but the percentage of oil in the pulp did not change. Girdling reduced shoot growth, but the internode length was unchanged. Girdling slightly stimulated differentiation of flower buds.
Diurnal and seasonal changes in photosynthetic characteristics, leaf area dry mass (ADM), and reducing sugar and total chlorophyll (Chl) contents of leaves of Frantoio, Leccino, and Maurino olive cultivars were investigated in Central Italy. Leaf net photosynthetic rate (PN) per unit leaf area changed during the growing season and during the day, but the cultivar did not significantly influence the changes. In both young and one-year-old leaves the highest PN values were observed in October, while the lowest values were recorded in August and December; during the day the highest PN values were generally found in the morning. The pattern of photosynthetic response to photosynthetic photon flux density (PPFD) of leaves was similar in the three genotypes. Sub-stomatal CO2 concentration (CI) tended to increase when PN decreased. The increase in CI was accompanied by a stomatal conductance to water vapor (gS) decrease. In general, PN and dark respiration rate (RD) were correlated. Transpiration rate (E), with no differences between the cultivars, increased from April to July, decreased greatly in August, then increased in October and finally decreased again in December. Leaf water content increased from April to June, remained high until mid July, decreased significantly in August, remaining constant until December with no differences associated with the cultivar. In both young and one-year-old leaves, the leaf water content per unit leaf area was slightly greater in Frantoio than in the other two cultivars. The one-year-old leaves had a higher Chl content than the young ones. The cultivar did not substantially influence the leaf reducing sugar content which decreased from April to August, when it reached the lowest level, then increased rapidly until October. During the day the reducing sugar content did not change significantly. The leaf ADM was slightly higher in Frantoio than in the other cultivars and one-year-old leaves had higher values than the young ones. Leaf ADM decreased from April to June and then tended to increase until December. During the day there were no substantial variations. and P. Proietti, F. Famiani.
The effect on traits of photosynthesis and water relations of assimilate demand was studied in olive tree that has strong alternate bearing. The diurnal and seasonal leaf gas exchanges, area dry mass, and saccharide and chlorophyll (Chl) contents were measured by comparing shoots with fruit of "on-trees" (heavy fruit load) with shoots without fruit on both "on-trees" and "off-trees" (light fruit load). In spite of large seasonal and diurnal differences, leaf net photosynthetic rate (PN), stomatal conductance (gs), sub-stomatal CO2 concentration (C1), transpiration rate (E), and respiration rate (RD) were not significantly influenced by fruit load or by the presence or absence of fruit on the shoot. An only exception was at the beginning of July when the one-year-old leaves on shoots with fruit had slightly higher PN and E than leaves on shoots without fruit. Water content, Chl and saccharide contents, and area dry mass of the leaf were not substantially influenced by the presence/absence of fruit on the shoot or fruit load. Hence the sink demand, associated with fruit growth, did not improve leaf photosynthetic efficiency in olive.
Dry matter (DM) of olive fruit (cv. Leccino) constantly increased from fruit-set (mid-June) to the end of October. The oil content increased rapidly from the beginning of August, about 40-50 d after full bloom (AFB), to the end of October. As the oil content increased, the saccharide content decreased. On a DM basis, fruit dark respiration rate (RD) and stomatal conductance (Gs) were high soon after fruit-set, then strongly decreased. Gross photosynthetic rate (PG) in full sunlight was high in the first 3 weeks after fruit-set, when the chlorophyll (Chl) content and the ratio between fruit surface area and volume were high, then it progressively decreased. The fruit intercellular CO2 concentration (Ci) was always relatively high, particularly from September onwards. The PG increased following the increase of irradiance (I). The daily PG trend was similar to the I and temperature trends, showing the maximum values at 14:00 h. For a large part of the fruit growing period, during daylight, the CO2 intake by a fruit permitted the reassimilation of a large part (40-80%) of the CO2 produced by RD. The stomata in the first stages of fruit growth were oval and surrounded by guard cells, two months later they lost their shape and were covered by wax. The reduction in fruit PG during fruit growth could be connected to the reduction of the ratio between fruit surface area and fruit volume and the cellular differentiation, whereas the constant high Ci seems to exclude the influence of Gs decrease. Even if olive fruit is highly heterotrophic organ, its photosynthesis can considerably reduce the use of assimilates for respiration and favour fruit maintenance and growth. and P. Proietti, F. Famiani, A. Tombesi.
From the beginning of olive leaf yellowing to leaf fall (1/3 months), there was a general trend from anabolism to catabolism. Rates of net photosynthesis (PN) and respiration, areal dry mass, and contents of pigments, particularly of chlorophyll (Chl) a, starch, and above all nitrogen (N) decreased. The detachment force decreased dramatically only in completely chlorotic leaves. Chl a : b ratio only declined in the last 10-20 d of senescence, when the total Chl contents diminished by about 70 %, after which the N content, PN, and efficiency of the photochemical energy conversion of the remaining Chl and N dramatically declined. Consequently, for most of the natural course of senescence PN remained relatively high. The reduction in PN was associated with the decreases in transpiration rate (E) and stomatal conductance (gs), but these probably did not cause the decline of PN. The recycling of saccharide compounds was low, while 50 % of the total N on a leaf area basis was relocated back before leaf abscission, changing the leaf from a carbon source to a mineral source. Therefore, considering that senescing leaves in olive trees contribute to carbon gain and allow the recycling of resources, it is essential to prevent the premature leaf abscission by avoiding deficits of water and mineral nutrients and by using pruning and training systems that allow good irradiation of all leaves in the crown.