Releasing Date*
|
|
21-Jan
|
7-May
|
11-Jun
|
18-Jun
|
4-Jul
|
10-Aug
|
5-Sept
|
24-Oct
|
Biological Predator
|
Biological Predator Status
|
Releasing rate (number/m2)
|
BUG A
|
Adult
|
3.7
|
0
|
4.9
|
4.9
|
4.3
|
2.9
|
8.6
|
8.6
|
Larvae
|
3.1
|
0
|
2
|
0
|
0
|
0
|
0
|
0
|
BUG B
|
Adult
|
0
|
1.4
|
0
|
0
|
1.4
|
0
|
0
|
0
|
Due to the current circumstances in the region because of Coronavirus the release of Dicyphini bug
Bwas delayed.
Two ways were used to detect Tuta absoluta infection: the first by calculating the number of
infected leaves per experimental unit, second, by calculating the total number of males on the
pheromone (Ten traps per greenhouse, five traps in the front and 5 at the back).
1. Number of biological control agents in the greenhouses
Dicyphini bug A was introduced 6 times during the season, whereas Dicyphini bug B was introduced
only twice according as shown in figure (1). Bug B was introduced twice to protect plants as it is
known for its rapid population growth. To maintain the biological control agents, Artemia food was
used as an alternative food for Bug B at the rate of 80 g/greenhouse.
At the beginning of this trial, predators reproduced successfully in the biocontrol greenhouse
(Figure 1). By the end of March, bug A decreased. While in the end of September, both the population
of bug A and B increased again.
Figure 1: Average number of adult predators of both bugs in the biogreenhouse.
The reduction in the adult of both bio-predators was found to be associated with the frequent use of
fungicides against powdery mildew and Botrytis (Figure 2). By mid of March, powdery mildew started
to appear and requiring fungicides application. Later, Botrytis aggravated the problem. Fungicides
were applied first by the end of March, then regularly. This led to a significant decline in the
predator populations (Figure 2). However, when stopping fungicides application, the predator
population increased significantly again (Figure 2).
Figure 2: Average number of adult predators in the biocontrol greenhouse. Red marks indicate the
number of fungicides applications.
2. Biocontrol predators’ distribution on the plant
Numbers of both bug A and bug B adults were monitored in both upper and lower parts of tomato
plants. It was observed that both biocontrol predators prefer the upper part compared to the lower
one (Figure 3). It was also observed that these biocontrol predators developed better on Valouro RZ
tomato cultivar as compared to other ones (Figure 3).
3. Monitoring Tuta absoluta population
The number of Tuta absoluta larvae were monitored in both greenhouses, however, the number of
Tuta-infected leaves calculated during the evaluation period was low. This due to the regular manual
removal of infected leaves by the workers; thus, no leaf was left for calculation during the
evaluation. Therefore, the number of weekly inventories of adult Tuta caught by pheromone traps was
adopted (Figure 4). No chemical interventions were required to control Tuta in the biocontrol
greenhouse. In fact, both Dicyphini bugs, in addition to regular removal of infected leaves,
effectively prevented spreading of Tuta infection. However, chemical intervention was needed 7 times
to control Tuta population in the chemical control greenhouse (Figure 4).
Figure 4: Number of Tuta males in the pheromone traps in both biocontrol and chemical control
greenhouse. Red crosses indicated when the insecticide application took place in chemical control
greenhouse
No insecticides were needed during the cultivation season in the biocontrol greenhouse. However, the
number of fungicide applications against Powdery mildew and Botrytis was higher in the biocontrol
greenhouse than in the chemical control greenhouse (Figure 5).Most of the chemical application in
the chemically controlled greenhouse were against Tuta, closely followed by Spidermites (Figure 5).
Spider mite outbreaks also occurred in the biocontrol greenhouse but were controlled by mass-release
of the predatory mites Neoseiulus califirnicus and Phytoseiulus persimilis.
Figure 5: Frequency and types of chemical pest used during the season (Jan-Dec. 2020) in the
biocontrol and chemical control greenhouse.
4. Tomato production
The accumulated yield of good fruit for the three cultivars in both greenhouses are presented in
figure (6). Tomato harvest was started from March,2020. Our results showed that yield of both Feisty
red and Valouro cultivars was higher in the biocontrol greenhouse as compared to the chemical
control greenhouse, while yield of Tone Guitar cultivar was higher in the chemical control
greenhouse as compared with biocontrol greenhouse. Good (marketable) yield in the biocontrol
greenhouse ranged from 79.3 to 85.2kg/m2, whereas good yield in the chemical greenhouse ranged from
77.3 to 87.4kg/m2.
Figure 6: Accumulated good yield of the three tomato cultivars in both biocontrol and chemical
control greenhouses.
Recommendation
Reproduction of Dicyphini bug A was significantly reduced due to frequent use of fungicides in the
biocontrol greenhouse, while releasing bug B during this period has less effect on the population
development. However, when stopping the application of fungicides, both bug A and bug B populations
increased. This could be due to frequent application of fungicides in biocontrol greenhouse compared
to the chemical control greenhouse because of limited application of sulfur in biological control
greenhouse to reduce the impact and protect predators from sulfur as far as possible. Fungicides
were often applied directly as spot treatment to the infected plant or the infected area. Although
this approach protects the bio-predators, it made difficult to eliminate fungal infections. Yet, the
full application of fungicides in biocontrol greenhouse enabled better control of fungal infections.
A striking result is that the three-weekly assessments show that there is no difference in strata
preference between bug A and bug B. Both seem to prefer the higher parts of the plant. Dicyphini bugs
lay their eggs and feed on soft plant tissue, which is more present in the top of the plant, which can
explain their preference for the higher plant parts. At the end of the growing season there were higher
numbers of bug B than bug B adults in the crop. This, while bug A was introduced 6 times and bug B only
2 times. The faster development of bug B, together with their overlap in strata preference probably
causes that bug A is ultimately outcompeted by Nesi.
No chemical interventions were needed in H2 against Tuta, while being present in the greenhouse since
the beginning of the growing season. A population of predatory bugs, in combination with the manual
removal of infected leaves, ensured a sufficient protection of a Tomato crop against Tuta.
The most troublesome pest turned out to be both Tuta and Spider mites. In the biocontrol greenhouse
Spider mite outbreaks were only controlled by frequently mass-releasing Neoseiulus californicus and
Phytoseiulus persimilis. The downside of these predatory mites is that they are expensive and do not
build up a population in the crop. Both die out in the absence of prey and the sticky trichomes of
Tomato limits their mobility. Controlling spider mites in Tomatoes remains a matter of intensive weekly
scouting and early interventions with predatory mites. Predatory mites can also be released in low
numbers on a regular basis to prevent an outbreak of Spider mites.
This trial has proven that tomatoes can be cultivated for a whole season (up to 12 months) with good
yield without using chemical insecticide in the Kingdom. The use of fungicides did not eliminate
bio-predators. Yet it reduced their population. Therefore, suitable control of temperature and relative
humidity should be maintained to prevent fungal infections and enhance bio-predators efficiency.