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Analyzing the mass-rearing system of the California red scale parasitoid Aphytis melinus (Hymenoptera: Aphelinidae).

In several citrus-growing regions of the world, the parasitoid Aphytis melinus DeBach (Hymenoptera: Aphelinidae) has been used for many years to control California red scale, Aonidiella aurantii (Maskell) (Hemiptera: Diaspididae). Also, this parasitoid has been commercially mass produced previously for augmentive release to control this scale pest in southern California lemon orchards (Moreno & Luck 1992) timed in the spring to coincide with the presence of virgin adult female California red scale, A. aurantii. Moreover, A. melinus also has been used to control another citrus pest, Aspidiotus nerii Bouche (Hemiptera: Diaspididae), in California and Spain (Grafton-Cardwell et al. 2011; Olivas et al. 2011).

Previously, several classic studies have examined the biology and host relationships of A. melinus under laboratory conditions (Collier 1995; Heimpel & Rosenheim 1995; Hare 1996; Heimpel et al. 1997), whereas other studies have examined the efficacy of this species under field conditions(Murdoch et al. 2006; Sorribas et al. 2012; Zappala et al. 2012). Initial bionomic and behavioral data from several of these studies provided the framework for mass- rearing procedures based on the work by DeBach and White (1960) with few studies on A. melinus production published since (Raciti et al. 2003; Zappala et al. 2006).

In this paper we present large scale mass-rearing production data of A. melinus during a 3-yr cooperative augmentive release program with a citrus-producing company to control California red scale in Spain. Identification and analysis of production parameters, as they influenced parasitoid abundance, focused on: (a) variables affecting physical production of parasitoids in rearing units, (b) effects of supplemental honey sources on parasitoid survival, and (c) variables affecting the parasitism of the host scale A. nerii.

Materials and Methods

REARING PROCEDURES

The A. melinus colony used in these studies was obtained from Koppert-Espana (La Mojonera, Almeria, Spain), which produced this parasitoid in their facilities at Aguilas (Murcia, Spain). In addition, we supplemented our colony with individuals collected in citrus groves along the Guadalquivir Valley in the province of Cordoba (Spain). Aphytis melinus was reared at the University of Seville, following the method developed for rearing Aphytis lingnanensis DeBach (DeBach & White 1960; Rose 1990; Raciti et al. 2003). This rearing method is used commonly in commercial insectaries for A. melinus production.

A parthenogenetic strain of the scale A. nerii reared on butternut squash (Cucurbita moschata Duchesne ex Lamarck [Cucurbitaceae]) (average size: 18.5 [+ or -] 0.3 cm L, 8.7 [+ or -] 0.2 cm W) served as a substrate host for A. melinus production. Infested squash, with third instar scales, was exposed to 2- to 3-d-old adult parasitoids (male and female) in a screened cage (41 cm W x 32 cm H x 52 cm D) provided with honey, ad libitum, in plastic dishes. Third instar A. nerii is the preferred host age for A. melinus to oviposit and maximize progeny production (Forster et al. 1995). One to 2 parasitoid releases were conducted in each cage. Parasitoids were removed using C[O.sub.2] after about 3 d and survival determined. Hosts and parasitoids were maintained in the laboratory at 25 [degrees]C, 60.0 [+ or -] 5% RH under continuous light.

At the end of 14 d, newly emerged adult A. melinus were collected every 2 to 3 d until production ceased in each rearing cage. During collection, adults were anaesthetized with C[O.sub.2] (the cage was first sealed and then the gas introduced through an inlet valve for 1 min) and dislodged from the squash surface and interior of the cage with an air blast. Adults then were collected from the white paper lining the bottom of each cage onto a piece of black cardboard (29.5 cm x 21 cm). A photograph was taken while adult parasitoids remained anaesthetized and total abundance recorded. Also, adult parasitoid survival and progeny production were evaluated with or without a supplemental carbohydrate source of honey in rearing cages. The supplemental source consisted of 5 to 10 drops of "rosemary honey" (Ynsadiet, Leganes, Madrid, Spain) smeared on the surface of squash.

HOST PARASITISM ON SQUASH

On average, 1 parasitoid production cycle (generation) was completed in about 20 d. At that time, scale-infested squashes were brought to the laboratory where 100 randomly selected adult scales were examined using a binocular stereomicroscope to record if they were dead, alive, or parasitized. A total of 136 squashes were examined from 72 rearing cages during the 5 mo study.

VARIABLES QUANTIFIED IN APHYTIS MELINUS PRODUCTION

A description of the associated variables that were measured for influence on A. melinus production are summarized in Table 1. Specifically, 8 variables were selected to predict total parasitoid production; these were: (1) number of adult A. melinus parasitoids added to a cage, (2) number of host A. nerii present on squash in each cage, (3) total squash surface available in each cage, (4) initial number of adult A. melinus added to each cage combined with amount of time to complete parasitism of hosts (referred to as "Momentum of A. melinus"), (5) ratio of third instar A. nerii presented in the cage to A. melinus introduced into each cage, (6) number of parasitoid-host exposure days, (7) number of parasitoid introductions into each cage to parasitize hosts, and (8) presence or absence of a supplemental source of carbohydrate (honey). For all variables where adult parasitoids were used, both sexes were represented. It was assumed that the sex ratio of A. melinus was around 3:2 (female:male) based on work by Gonzalez-Zamora et al. (2015).

The squash surface was estimated using the surface of a cylinder or the surface of a truncated cone, depending of the shape of the particular squash. Length and diam of the squash were the parameters used to estimate squash surface. The density of A. nerii on squash was estimated with the assistance of a piece of cardboard with a 1 [cm.sup.2] hole cut into it. The hole was placed randomly on at least 9 places on the surface of each squash and the average number of A. nerii per [cm.sup.2] was calculated. Using the estimated squash surface and the density of the parasitoid, the estimated total host population on the surface was determined.

STATISTICAL ANALYSIS

Production variables were analyzed first to meet the requirements of normality, and transformed if necessary (Table 1). There were no correlations between the explicative variables, except for "Momentum of A. melinus" and "A. melinus added" (r varied between 0.82 and 0.90, with P < 0.01). "Momentum" was therefore excluded from further analysis.

The General Linear Model procedure was applied to total individuals (hosts and parasitoids) per cage as well as individuals (hosts and parasitoids) per [cm.sup.2] of squash per cage. The analyses initially included 8 independent (or explicative) variables in the model. Those variables that were not significant (P > 0.05) were eliminated in subsequent steps from the regression model. Comparison of adult A. melinus mean survival with or without a supplementary source of carbohydrate (honey) on squash was analyzed with Student's t test, P < 0.05.

Parasitism of A. nerii on squash was analyzed using a logistic regression in which the dependent variable, frequency of parasitism recorded, was expressed as a percentage. Average cage data from 64 cages were used initially for this analysis. Total parasitism summed values of (1) scales with emerged parasitoids, (2) scales containing parasitoid larvae or pupae, and (3) scales with dead parasitoids. These values were expressed as a percentage of all scales present. One of the response variables ("A. nerii presented") (see Table 1) was converted from a continuous distribution to a categorical one with 5 divisions or groups. Data from cages with studentized residuals > 3 were not included in the analysis; the final number of cages included in the analysis was 58. Two logistic regression analyses were performed: (1) applied to the independent variables expressed as total number of host or parasitoid per cage, and (2) applied to the independent variables expressed as host or parasitoid per [cm.sup.2] of squash per cage. The second analysis above is presented in results because it contained fewer significant variables (4 total) compared with the first analysis on host or parasitoid per cage. All statistical analyses were performed with Statgraphics Centurion XVI v16.1.07 (Stat Point Technologies 2010).

Results

ANALYSIS OF PRODUCTION

Results from statistical analyses of A. melinus production data are provided in Table 1. The last column includes the transformation applied to variables that did not meet statistical requirements. Coefficients of variables "A. melinus added" and "scale to parasitoid" ratio significantly affected production positively (Table 2). These results indicated that adding additional A. melinus adults to each cage and increasing the number of available host scales per adult parasitoid (ratio of scales per parasitoid) led to higher production of the parasitoid.

Aphytis melinus production varied from cage to cage with an average of 1,122 [+ or -] 93 (SE) individuals per cage (Fig. 2b). Emergence of adult A. melinus from their scale hosts started about 14 d after initial introduction of the parental generation, and reached its peak within the first 3 d of parasitoid emergence (Fig. 1a). Fifty percent of the total population emerged by the d 4, and 95% reached by the d 12 (Fig. 1b). The application of honey to the squash surface did not significantly increase adult A. melinus survival compared with no honey application, and combined survival averaged about 25.4 [+ or -] 1.1% (t = -0.84, P = 0.40).

HOST PARASITISM ON SQUASH

We found that as the variable "A. melinus obtained" significantly increased, the probability of obtaining higher parasitism on host A. nerii also increased (Table 3). The variable "A. nerii on squash" indicated that the optimum density of host scale available for parasitism was [less than or equal to] 10 scales per [cm.sup.2]. The other 2 significant variables from the logistic analysis were "Momentum of A. melinus" and "Honey on the squash" where both odds ratio were < 1. As the variable "Momentum of A. melinus" (as defined previously) increased, the probability of A. nerii parasitism significantly decreased. However, adding 2.6 parasitoids per d per [cm.sup.2] squash to cages was the optimum density to maintain efficient parasitism of hosts. Also, there was a lower probability of A. nerii parasitism in the absence of honey on the surface of squash compared with its presence (Table 3). We observed that approximately 47% of the A. nerii population on squash was parasitized, whereas 43% of the host population was dead.

Discussion

Mass production of beneficial insects is an important aspect of biological control implementation, especially for augmentative release programs. Most of the work devoted to the mass-rearing of beneficial insects is related to their biology or their relationship with the host (Ghimire & Phillips 2010; Saleh et al. 2010; Whistlecraft et al. 2010), as well as the analysis of production mechanics for improved efficiency (Canale & Benelli 2012; Vacari et al. 2012; Tormos et al. 2014). Another facet of beneficial insect mass production commonly analyzed is the general quality of the product produced (Vasquez & Morse 2012; Veiga et al. 2013). Our results suggested that production of A. melinus was affected primarily by the number of adult parasitoids introduced in cages to initiate production and scale to parasitoid ratio; as the number of hosts available per parasitoid increased, so did the productivity of parasitoids in the rearing cages. The importance of keeping an adequate scale to parasitoid ratio has been suggested to be about 5 to 10 scales per parasitoid on a daily basis (Gonzalez-Zamora et al. 2015).

We routinely provided honey, in plastic dishes, when mass-rearing A. melinus because a sugar source is considered critical to parasite survival (Heimpel et al. 1997; Wackers 2003). Interestingly, supplemental application of honey to the surface of squash did not improve adult parasitoid survival, but did increase the percentage of parasitized scales. We also observed a high percentage (43.1%) of scales on squash were either dead, most probably due the host feeding activity of A. melinus adults, or parasitized (46.9%), with only a small percentage surviving (9.9%). Many authors have observed host feeding behavior of A. melinus in laboratory and field studies (Collier 1995; Heimpel et al. 1997; Sorribas & Garcia-Mari 2010). This behavior appears to be fundamental in their biology because it increases longevity and lifetime fecundity. This is especially true for those that are idiobiont parasitoids with a synovigenic egg load (as A. melinus) (Thompson 1999; Wackers 2003; Strand & Casas 2008; Tena et al. 2015).

Additionally we found that the lower host density appeared to promote a higher probability of being parasitized compared with higher host density. One possible explanation is that as host density increased, the capacity of parasitoids to parasitize them was not linear. We also observed that increasing the initial number of parasitoids in a cage or the exposure time of A. melinus to hosts (referred to as "Momentum of A. melinus") decreased the probability of parasitism. It is possible that as more parasitoids are introduced, or exposure time to hosts lengthened, more hosts can be killed by host feeding. Similar results have been obtained in previous laboratory tests by Gonzalez-Zamora et al. (2015). In summary, we found the number of A. melinus adults initially introduced into rearing cages, and the host scale to parasitoid ratio during the rearing process profoundly affected subsequent parasitoid production. Optimizing the density of hosts can improve parasitism levels and hence the productivity of the system.

Acknowledgments

We thank Jean-Claude Malausa and Nicolas Ris from the INRA Vallbonne (France) for the uniparental strain of Aspidiotus nerii. We acknowledge all the help and support given by the Servicio de Sanidad Vegetal (Conselleria de Agricultura of the Generalitat Valenciana, Valencia, Spain), with special thanks to Jose Luis Porcuna, Alberto Garcia, and Carmen Laurin. This work was funded by Rio Tinto Fruits S.A. (El Campillo, Huelva, Spain), with the help of the regional government of Andalucia (Junta de Andalucia, Seville, Spain), within the research project "Cria de Aphytis melinus y Comperiella bifasciata para el control biologico del piojo rojo de California en citricos."

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Jose E. Gonzalez-Zamora (1*), and Maria L. Castillo (1,2)

(1) University of Sevilla, Department of Ciencias Agroforestales, Seville, Spain; E-mail: zamora@us.es (J. E. G. Z.)

(2) Agricultura y Ensayo S.L., Alcala de Guadaira, Seville, Spain, E-mail: mcastillo@agriculturayensayo.com

(*) Corresponding author; E-mail: zamora@us.es

Caption: Fig. 1. Parasitoid (Aphytis melinus) production (as percentage of the total production given as mean [+ or -] SE) in the production cages: (a) daily emergence; (b) cumulative emergence.

Caption: Fig. 2. Production of Aphytis melinus over the period in which the pilot system was working, from 18 March 2010 to 20 Jun 2011: (a) Total production per day, when different cages were in production at the same time and collection was every 2 to 3 days; (b) Total production per cage. Each bar in (b) represents the production of an individual cage, and is displayed as the date when parasitoid emergence began.
Table 1. Variables used in the analysis of Aphytis melinus production,
with their average values and standard errors (SE).

                                             Average values
Variable              Description            (SE)

A melinus obtained    per cage, or per        1122 (93)
                      [cm.sup.2] squash
                      per cage
A melinus added       per cage, or per        1279 (84)
                      [cm.sup.2] squash
                      per cage
A. nerii presented    per cage, or per           9.4(0.8)
                      [cm.sup.2] squash
                      per cage
Squash surface        Total surface per       1208 (34)
                      cage ([cm.sup.2])
Momentum of           per cage, or per        3588 (307)
A. melinus            [cm.sup.2] squash
                      per cage
Ratio Scale to        Ratio between both         9.8 (0.7)
Parasitoid            populations in the
                      cage
Days with A. melinus  Number of days that        3.0 (0.1)
                      A melinus were in the
                      cage parasitizing the
                      host
Number of             Times that A. melinus      1.4(0.1)
inoculations          was introduced in
                      the cage
Honey on squash       Presence or absence       33 (with honey)
                      of extra honey on         95 (without honey)
                      the squash surface

                                                      Statistical
Variable            Units                             transformation

A melinus obtained  A. melinus produced per cage      Square root
A melinus added     A. melinus added per cage         Square root
A. nerii presented  A. nerii per [cm.sup.2] per cage  Logarithm
Squash surface      [cm.sup.2] of squash per cage     Logarithm
Momentum of         Total A. melinus x days in        Logarithm
A. melinus          the cage to parasitize the
host
Ratio Scale to      Ratio Scale to Parasitoid         Logarithm
Parasitoid          in the cage
Days with A.        Number of days of A
melinus             melinus parasitizing
                    in the cage
Number of           Times that A melinus
inoculations        were introduced in the cage
Honey on squash     Cages with or without
                    honey on the squash surface

n = 128 cages and 252 squash, average of 2.0 [+ or -] 0.1 squash per
cage.

Table 2. Significant variables with their coefficients and standard
errors (SE) from the General Linear Model analysis, of Aphytis melinus
production per cage and per [cm.sup.2] squash per cage.

         Production of A. melinus per cage (a)
Variable                  Coefficient     SE

Constant                  -26.93          4.04
[??] (A. melinus added)     1.09          0.08
Log (Scale/Parasitoid)     10.62          1.19
                  [F.sub.2,114] = 116.40
                  p < 0.001
                  [R.sup.2] = 0.67
                  SE = 8.71

 Production of A. melinus per [cm.sup.2] squash per cage (b)
Variable                                 Coefficient   SE

Constant                                 -0.74         0.12
[??] (A. melinus added per [cm.sup.2])    1.04         0.08
Log (Scale/Parasitoid)                    0.31         0.04
                             [F.sub.2,114] = 106.90
                             p < 0.001
                             [R.sup.2] = 0.65
                             SE = 0.26

(a) Dependent variable is V (A. melinus obtained per cage).
(b) Dependent variable is V (A. melinus obtained per [cm.sup.2] of
squash per cage).

Table 3. Significant variables with their odds ratio and confidence
limits (at 95%) in the logistic regression analysis of total
parasitized Aspidiotus nerii (expressed as percentage) on squash used
in the rearing of Aphytis melinus. Variables used in the analysis are
expressed per [cm.sup.2] squash per cage (when pertinent).

                                      95%          95%
Variables                 Odds ratio  Lower limit  Upper limit

A. melinus obtained       1.399       1.287        1.522
(per [cm.sup.2])
A. nerii on the squash
(per [cm.sup.2])
  Level=A (a)             1.803       1.506        2.158
  Level=B                 1.489       1.278        1.733
  Level=C                 1.012       0.868        1.180
  Level=D                 1.095       0.943        1.271
Momentum (b) of A.        0.882       0.853        0.912
melinus (per [cm.sup.2])
Honey on squash
  Level = 0 (c)           0.785       0.709        0.869

The model was significant (P < 0.0001), and explained 0.65 of the
variability of the data (n = 58 cages from the original 64 cages used
to analyze the parasitism observed on Aspidiotus nerii).
(a) A. nerii per [cm.sup.2]: A [less than or equal to] 3.0, B = 3.1 to
7.0, C = 7.1 to 11.5, D = 11.6 to 15.0, E [greater than or equal to]
15.1 (used as reference level).
(b) It is the initial parasitoid number by duration of parasitism.
(c) Level = 0 (no honey on the squash), Level = 1 (honey on the squash,
used as reference level).


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Author:Gonzalez-Zamora, Jose E.; Castillo, Maria L.
Publication:Florida Entomologist
Article Type:Report
Geographic Code:4EUSP
Date:Sep 1, 2018
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