Field test Field test

This experiment was carried out in a Citrus aurantifolia orchard in the Lodana Parish of the Santa Ana town in Manabí, Ecuador (01°12´ S and 80°23´ W); each experimental plot consisted of nine six years old trees (separated seven meters between rows and seven meters between trees), being the central tree the useful one. The treatments were: aqueous extract of neem (50 gL^-1), formulated neem oil Inbio 75 ™ -CEMADEC- (10 mL^-1), and an absolute control (water). A randomized complete block design was used, with four blocks. Treatments applications were decided based on three parameters: a) CLM infestation around 30%, b) presence of instars I and II of CLM larvae c) Flushing greater than 60%. Treatments were applied with a motorized knapsack sprayer Solo™, using the flow restrictor in the position four, which generated the expense of one liter of insecticide solution per tree. Evaluations took place each 48 hours until 10 days after the application of treatments. The repellent effect of neem on adults of CLM was calculated using the percentage of infestation in 20 fresh previously tagged shoots per useful tree and applying the formula cited by ^{González et al., (1995)}:

Equation 1 :

To establish CLM larvae mortality, prior to application of the treatments leaves without mines were eliminated in each tagged shoot, leaving only those with presence of live CLM larvae, of first instar, which is a stage suitable for A. citricola oviposition (^{Edwards and Hoy, 1998}). A 10 x magnifying glass was used to recognize the CLM larvae After the application of treatments, the selected shoots were protected with organdie bags, in order to avoid effect of predation and other parasitoids over CLM larvae. Larval mortality was determined visually in the field, using an OptiVisor ™ magnifier glass (4x) and applying the formula cited by ^{Tierto (1994):}

Equation 2 :

The effect of neem on parasitism was determined based on the following variables: live larvae, dead larvae, adults emerged from CLM and pupa with evidence of parasitism, obtaining the percentage of parasitism in each evaluation, by the formula cited by ^{Castaño (1996):}

Equation 3 :

This experiment was repeated three times during the dry season.

Cage test

This experiment was carried out at the “Portoviejo” Experimental Station of the National Institute of Agriculture Research (INIAP) (01°10´ S and 80°26´ W). 150 one year old plants of mandarin "Cleopatra" (C. reticulata) were placed in a cage (2 x 2 x 2 m) covered with organdie cloth, and were distributed in three groups of 50 plants per treatment, that were pruned a height of 50 cm with the purpose of stimulating the uniform emission of new shoots, free of CLM, after 15 days in the cage the plants had shoots of 5 cm which are ideal for infestation(^{Bautista,1998}). The same three treatments of the field test were assigned in a randomized complete design in which each plant was considered as an experimental unit; the treatments were applied using a manual backpack sprayer CP3™ with a expense of 10 mL of the insecticide solution per plant, each group of plants was treated in different times to avoid contamination, after this process plants were immediately transported to an open field. They remained in a citrus orchard with historical records of high levels of CLM and parasitoids during eight days, in order to allow CLM infestation, larvae development until instar I and exposition to parasitoids. At the end of this period, the plants were moved back to the cage to suppress the risk of predation of CLM larvae. Neem repellency on CLM adults and parasitoids was determined, as well as CLM larval mortality by neem effect. The test was repeated twice (dry season and rainy season ).

Olfactometer test

This trial was done in the laboratory of entomology in the “Portoviejo” Experimental Station (26 ± 2 °C and 75 ± 5% RH, 12-h photoperiod). Neem repellency was studied using CLM adults. The test was repeated twice. It was applied the methodology described by ^{Schuster et al.,(2009)}, using plastic olfactometers which consisted in transparent jars of a size of 20 cm in height by 16 cm in diameter, in the upper part it was made a hole of 3 cm, which was covered later with a plug. Tests started every day at 6:00 h, using cutting discs (one per each olfactometer) of C. aurantifolia young leaves of 2.5 cm diameter, which were immersed in the same treatments of field test for 10 seconds, then placed in a mesh for 30 minutes for drying. Later they were collocated in the hole located at the top of each olfactometer (inside the plug) and supported with a mesh. Evaluations began at 7AM and from this first record, data was taken at 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 and 24 hours after. The only variable recorded was the number of adults perched on the leaf disc, one replicate per day, with a total of five biological replicates of the experiment, each one was considered as a repetition in a completely randomized design, the experimental unit was a olfactometer with 20 unsexed newborn (<24 h) adults of CLM. The percentage of repellency was calculated whit the formula used by ^{Olivero et al., (2009)}:

Equation 4 :

Preparation and application of treatments

For the treatment with aqueous extract, the operation was controlled from the harvest to the processing of the mature neem seed, which was harvested and immediately processed (deshelled, washed with water and dried at room temperature for five days), under these conditions the seed was ready to be ground. In each application the necessary amount of seed was ground and mixed with water, 24 hours later this solution was strained twice (with the objective of avoid blocking of the nozzles of the sprayer) and applied at the concentration of 50g L^-1. For the neem oil treatment it was used the commercial formulated oil INBIO 75™ at the concentration of 10 mL L^-1.

Statistical analysis

Data was analyzed with the Statistical Analysis program, Version 6.12 (^{SAS Institute, 1988}), Tukey mean separation test was applied to variables that showed statistical differences (p ≤ 0.05).

Field test

Neem repellency to adult CLM populations was determined based on the percentage of infestation (Figure 1A). Tukey test detected in all replicates that the aqueous extract and formulated neem oil treatments differ statistically from the control, which presents up to 47.96% infestation in replicate one. In replicate three, it is observed that statistically the aqueous extract differs from the other two treatments, presenting the lowest infestation (11.97%), followed by the neem oil formulated with 18.41%. This suggests that neem acts as a repellent for adults of CLM, by keeping it away from the plant by olfactory or gustatory ways, interfering with its oviposition (Botanical Agricultural Insecticide, 1996). This is also consistent with the work of ^{Zhang et al., (1994)} in China, who applying neem oil in concentration of 1.4 %, obtained infestations lower than 10 %, while the control reached 97 %.

Larval mortality in plots treated with neem differ statistically from the control in the three trials, presenting continuously a high value, which reaches 77.17 % in the aqueous extract and 68.96 % in the oil (Figure 1B), concordant with ^{Bautista (1997)}, who states that the aqueous extract of neem (50 gL-1) causes a mortality of 70.56 % between 48 and 72 hours after application, while Valarezo and Cañarte (1998) report a mortality of the formulated oil (Inbio 75™) higher than 80 % until 12 days after application. It was also determined in this study that larval mortality began 48 hours after application and reached its maximum effectiveness ten days after application. The onset of neem mortality 48 hours after application, suggest that either as an extract or formulated oil, neem acts as an anti-feedant on the larvae of this pest. The limonoids contained in the neem paralyze the muscles of the jaws, interfering with the feeding process and eventually causes the death of the insect (Botanical ^{Agricultural Insecticide, 1996}). The anti-feeding action is manifested in the gastro-intestinal tract of the insect, so the ingested azadirachtin, causes disorders in the process of digestion and assimilation, this effect was confirmed by ^{Ghoneim and Hamadah (2017}) in an experiment with Spodoptera littoralis, in which they found that larvae treated with neem, defecated a significative lower amount of pellets that control ones. Another favorable and complementary characteristic of neem is its translaminar action (^{Botanical Agricultural Insecticide, 1996}). Action that allows it to reach the walls of the parenchyma where the larva feeds, causing disorders in the process of protein synthesis (^{Sponagel, 1997)}.

The biological effectiveness shown by neem on CLM larvae interferes with the parasitoid population (Figure 1C). Treatment means in the last evaluation for the parasitism variable show statistical differences between neem and control, which presented significantly higher parasitism percentages (66.04 %, 62.26 % and 53.30 %) for tests 3, 2 and 1 respectively. On the other hand, it was determined that being the treatments with neem statistically different to the control, also between them there are statistical differences, presenting the treatment with aqueous extract the lowest percentage of parasitism (not greater than 12.42 %) in test 3; while neem oil reached a parasitism of 23.30 % in test 1. The variation of parasitism between neem treatments is related to the differential mortality of larvae that present, since the aqueous extract presented a higher mortality, reducing the possibilities of establishment and development of parasitoids due to the suppression of the host. The parasitoid A. citricola was found parasitizing more than 50 % of CLM larvae in the control treatment and knowing that neem is responsible for high mortality of larvae, it also interferes with A. citricola, eliminating it during its development on the larva of CLM, This is verifiable when observing the Figure 1D, the control treatment always presents a significative higher percentage of CLM pupae (38.11 %, 31.95 % and 25.11 %), and that corresponds to those larvae that escape the action of parasitoids.

Olfactometer test

Tukey test to average number of adults of CLM perched on treated leaf disc, stablished that neem treatments are statistically different from the control in all evaluations and tests (Figure 3). The neem treatments do not differ statistically between them, in test 1 the aqueous extract had a maximum average of adults (1.60) at 12 hours, followed by neem oil that at 8 hours presented 2 adults, and while in the control were presented at 12 and 24 hours an average of 15.60 adults (Figure 3A). These results were confirmed in test 2: the control reached up to 14.20 adults posed at 12 and 24 hours, a situation very contrasting with neem treatments, where the maximum number of adults posed was 1.80 in neem oil at 24 hours and 1.40 adults at 8 hours in the aqueous extract (Figure 3B). These results agree with those previously found in this research, regarding to the repellent action that neem exerts on the adult populations of CLM, either in aqueous extract or formulated oil. Once this repellent effect was statistically verified, the values were transformed to percentage in the two tests. It was determined that both the aqueous extract and the formulated neem oil have, on average, very similar repellency, this being 85.68 % and 85.64 % for the extract and oil formulated, respectively in test 1, a situation that is confirmed in test 2, where on average a repellency was obtained for the aqueous extract of 88.80 % and 83.46 % for the formulated oil of neem.

Figure 1 : Field test, percentages of A) infestation of CLM, B), mortality of CLM, C) parasitism (A. citricola) and D) pupation of P. citrella.  

Figure 2 : Cage test, percentage of A) infestation of CLM, B) mortality of CLM, C) parasitism (A. citricola), D) adult emergence of P. citrella.  

Figure 3 : Olfactometer test, number of adults perched in leaf discs after the treatments. A) test 1, B) test 2.