Posts Tagged: off
Pruning Cherimoya for Off-season Fruit
A recent trip to Spain was an opportunity to look at their cherimoya production practices. One of the most interesting is their ability to manage the tree through pruning to produce fruit off-season (in spring) when the prices are the highest. IN California our low period of production is in the summer. The climate in Spain along the Mediterranean coast is warmer and more humid than coastal California, so most tree crops are about two months advanced in their production. So in the text I refer to a period when something is done and then follow it with another date. The one in parenthesis is the probable time in California if the date in Spain is used. So, to produce fruit in spring (summer) in March/April when prices are high:
Remove all shoots from the previous year in March (May)
With the new shoots, prune them back 6 inches in length around July 15 (September 15)
Pollinate the flowers that are produced in the period of August to September (Sept/Nov)
Pick fruit in March/April (June/Aug)
Advantages:
Fruit is produced when prices are higher
Generally fewer seeds than at other periods
In some cases there is higher sugar content in the off-season frui
Disadvantages:
Not always consistent with all cultivars
Off-season fruit often has black spots in the pulp
May see increased leaf drop
In some cultivars, the skin is more prone to abrasion, and this is already a very delicate fruit
There are other fruit species that fruiting date can be manipulated by pruning, such as evergreen blueberries, guava, lime, mango and carambola (star fruit). Always it is to find a better market for the fruit.
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cherimoya
PGRs aand Olives
Advances in mitigation of alternate bearing of olive: vegetative growth response to plant growth regulators
Elizabeth Fichtner, UCCE Farm Advisor, Tulare County, and Carol Lovatt, Professor of Plant Physiology, Botany and Plant Sciences, UC-Riverside.
Alternate bearing (AB) is a phenomenon in olive where fruit production alternates between large crops consisting of smaller, lower value fruit during an ‘"ON’ year and smaller crops consisting of larger, higher value fruit during an "OFF" year. The large swings in biennial olive production impact the overall industry, from growers to harvesters, to processors. In olive, the vegetative growth in one year produces the nodes bearing potential floral buds in the spring of the second year. Fruit suppress vegetative shoot growth resulting in fewer nodes available to bear fruit the following year. Our phenological studies have helped characterize the relationship between fruit load and vegetative growth on ‘Manzanillo’ olives in Tulare County, California.
Investigation of vegetative growth response to plant growth regulators
One strategy proposed to mitigate AB is to stimulate summer vegetative shoot growth to increase the number of nodes with the potential to produce floral buds. To address this strategy, our research team designed and implemented a proof-of-concept study in which plant growth regulator (PGR) treatments were injected into individual scaffold branches on opposing sides of ’ON‘ and ’OFF‘ trees. Plant growth regulators utilized in the study included two cytokinins, 6-benzyladenine (6BA) and a proprietary cytokinin (PCK), as well as two auxin-transport inhibitors, tri-iodobenzoic acid (TIBA) and a natural auxin transport inhibitor (NATI). Eight PGR treatments were included, with each PGR tested alone, and each cytokinin tested in combination with each auxin-transport inhibitor. PGR treatments were implemented in Summer (July 2012), and Summer + Spring (July 2012 and February 2013). Vegetative shoot growth was recorded monthly throughout the year to determine the influence of PGR treatments and timings on node production. The study was completed at the Lindcove Research and Extension Center (Exeter, CA).
Node production in response to plant growth regulator treatments
Scaffold injection with numerous PGR treatments resulted in significant increase in vegetative shoot growth. For example, nonbearing shoots on ‘ON’ control trees, produced an average of one node between July 2012 and February 2013, whereas nonbearing shoots on PGR-treated scaffold branches exhibited almost 4 times the new growth of the control trees (Table 1, shaded). Importantly, the new growth in some cases was statistically equal to and numerically greater than the new vegetative shoot growth of nonbearing shoots on ‘OFF’ control trees. The PGR treatments also had a positive effect in increasing vegetative shoot growth on bearing shoots of ‘ON’ crop trees. Bearing shoots on ‘ON’ control trees produced an average of 0.8 nodes between July 2012 and February 2013, whereas bearing shoots on PGR-treated scaffold branches of ‘ON’ trees produced over three-fold more nodes during this period. Some PGR treatments increased the number of new nodes on bearing shoots on ‘ON” trees to values equal to those of nonbearing shoots of ‘OFF’ crop control trees (Table 1, asterisk). Identify the better treatments. On average two additional nodes of growth were added to shoots in all treatments from February through April. Thus, in April shoots treated with some PGRS (Table 1, shaded) remained longer than bearing or nonbearing shoots on ‘ON’ crop control trees and equal to nonbearing shoots on ‘OFF’ crop control trees. This result suggests that with regard to increasing vegetative shoot growth there was no advantage derived from supplementing the Summer PGR treatment with the second Spring PGR treatment. However, the effect of the Spring PGR treatments on floral bud break and return bloom and fruit set remains to be determined.
Table 1. The effect of scaffold branch injected plant growth regulator treatments on vegetative shoot growth, as number of new nodes produced. |
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|
|
New Nodes |
|
Treatment |
Branch Status |
July-February |
July-April |
ON Control |
Fruit |
0.8 l |
3.3 jkl |
TIBA+6BA SUMMER |
Fruit |
2.3 hijk* |
4.6 cdefghij |
TIBA+PCK SUMMER |
Fruit |
2.5 ghij* |
4.9 bcdefghij |
NATI+6BA SUMMER |
Fruit |
2.7 fghij* |
4.2 fghijkl |
NATI+PCK SUMMER |
Fruit |
2.2 hijk* |
3.9 hijkl |
TIBA SUMMER |
Fruit |
2.4 hij* |
4.9 bcdefghij |
NATI SUMMER |
Fruit |
2.5 fghij* |
4.3 efghijkl |
6BA SUMMER |
Fruit |
2.2 ijkl |
4.2 fghijkl |
PCK SUMMER |
Fruit |
2.6 fghij* |
4.7 cdefghij |
TIBA+6BA SUMMER+SPRING |
Fruit |
2.4 hij* |
4.5 defghijk |
TIBA+PCK SUMMER+SPRING |
Fruit |
3.0 efghi* |
4.5 defghij |
NATI+6BA SUMMER+SPRING |
Fruit |
2.6 fghij* |
5.0 abcdefghij |
NATI+PCK SUMMER+SPRING |
Fruit |
2.2 ijk* |
3.7 ijkl |
TIBA SUMMER+SPRING |
Fruit |
2.0 ijkl |
4.1 ghijkl |
NATI SUMMER+SPRING |
Fruit |
3.1 defghi* |
5.5 abcdefghi |
6BA SUMMER+SPRING |
Fruit |
2.7 fghi* |
4.9 bcdefghij |
PCK SUMMER+SPRING |
Fruit |
1.3 jkl |
2.5 l |
OFF Control |
No Fruit |
3.6 abcdefgh |
5.0 bcdefghij |
ON Control |
No Fruit |
1.0 kl |
2.7 kl |
TIBA+6BA SUMMER |
No Fruit |
3.8 abcdefg |
4.7 cdefghij |
TIBA+PCK SUMMER |
No Fruit |
4.7 ab |
5.9 abcdefg |
NATI+6BA SUMMER |
No Fruit |
4.8 a |
6.3 abcd |
NATI+PCK SUMMER |
No Fruit |
4.5 abc |
6.0 abcde |
TIBA SUMMER |
No Fruit |
4.4 abcd |
6.0 abcdef |
NATI SUMMER |
No Fruit |
4.2 abcde |
4.9 bcdefghij |
6BA SUMMER |
No Fruit |
3.4 bcdefghi |
4.0 hijkl |
PCK SUMMER |
No Fruit |
4.3 abcde |
5.5 abcdefghi |
TIBA+6BA SUMMER+SPRING |
No Fruit |
4.2 abcde |
5.2 abcdefghi |
TIBA+PCK SUMMER+SPRING |
No Fruit |
4.8 a |
5.7 abcdefgh |
NATI+6BA SUMMER+SPRING |
No Fruit |
3.9 abcdef |
5.1 abcdefghi |
NATI+PCK SUMMER+SPRING |
No Fruit |
3.2 cdefghi |
4.2 efghijkl |
TIBA SUMMER+SPRING |
No Fruit |
4.8 a |
6.5 ab |
NATI SUMMER+SPRING |
No Fruit |
4.5 abc |
6.8 a* |
6BA SUMMER+SPRING |
No Fruit |
4.8 a |
6.4 abc |
PCK SUMMER+SPRING |
No Fruit |
3.6 abcdefgh |
4.7 cdefghij |
P-value |
|
<0.0001 |
<0.0003 |
Note: shading denotes treatments significantly different than ON Control + Fruit treatment. Asterisk denotes treatments significantly different than OFF Control (- Fruit). |
Summary
These preliminary data demonstrate that PGRs increase shoot growth, which might result in more nodes with the potential to produce inflorescences the following spring. Future studies are anticipated to address the use of promising treatments in foliar applications. Naturally-occurring compounds, such as PCK and NATI, may be easier and less costly to register than PGRs, which are classified as pesticides. Therefore, significant growth response to the natural compounds tested may have commercial benefit even if proven less efficacious than the synthetic PGRs.
Acknowledgements: The financial support of the California Olive Committee and the technical support of the Lindcove Research and Extension Center were integral to the success of this project.
olive tree