Establishment of the West Indian fruit fly (Diptera: Tephritidae) parasitoid Doryctobracon areolatus (Hymenoptera: Braconidae) in the Dominican Republic.
Abstract: The West Indian fruit fly, Anastrepha obliqua (Macquart), infests numerous fruit species, particularly Anacardiaceae and most importantly mango (Mangifera indica L.). Widespread in the Neotropics, it was first reported in Hispaniola nearly 70 years ago. Continental populations are attacked by the opiine braconid parasitoids Utetes anastrephae (Viereck) and Doryctobracon areolatus (Szepligeti). Largely sympatric, the two species co-exist through microhabitat specializations based on different ovipositor lengths and asymmetries in larval competitive abilities during multiparasitism. Utetes anastrephae, but not D. areolatus, is apparently native to the Dominican Republic. Since the two parasitoids share an evolutionary history over a substantial portion of their distributions it was proposed that 1) D. areolatus would find the Dominican environment suitable, as does U. anastrephae; and 2) that there would be no negative interactions when the two species were reunited and overall parasitism would increase. Immediately following releases, D. areolatus averaged 9% of adult insects recovered and two years after releases were concluded constituted a mean of 13%. By then the parasitoid had spread up to 50 km from release sites. There was no evidence of competitive exclusion of U anastrephae by D. areolatus. Another opiine biological control candidate, Diachasmimorpha longicaudata (Ashmead), could be considered for release and establishment. Parasitoids alone are unlikely to provide economic levels of control, but can serve as components of an integrated pest management program established to maintain "fly-free" or "low prevalence" fruit export zones.

Key Words: Anastrepha obliqua, mango, biological control, invasive pest

La mosca de las frutas de las Indias Occidentales, Anastrepha obliqua (Macquart), infesta numerosas especies de frutales, principalmente anacardiaceas, siendo el mango (Mangifera indica L.) especie de mayor importancia. Aunque este tefritido esta ampliamente distribuido en el Neotropico fue registrado hace 70 anos en La Hispaniola. Las poblaciones continentales de A. obliqua son atacadas por los parasitoides braconidos Utetes anastrephae (Viereck) y Doryctobracon areolatus (Szepligeti). Las dos especies de parasitoides co-existen a traves de especializaciones basados en diferencias en la longitud del ovipositor y asimetrias en las habilidades competitivas durante el multiparasitismo. Utetes anastrephae, pero no asi D. areolatus, es nativo en la Republica Dominicana donde ataca especies de Anastrepha nativas. Como las dos especies de parasitoides comparten una historia evolutiva sobre una porcion sustancial de su rango de distribution, se pronostico que: 1) D. areolatus se adaptaria al ambiente dominicano, tal como lo hace U. anastrephae; y 2) no existirian interacciones negativas cuando las dos especies esten juntas y que el parasitismo total se incrementaria. Inmediatamente despues de las liberaciones se recupero un 9% de adultos de D. areolatus y dos anos despues de finalizadas las liberaciones se recobro un 13%. El parasitoide se disemino por lo menos hasta 50 km de los sitios de liberacion. No se observaron evidencias de exclusion competitiva de U. anastrephae por D. areolatus. Se recomienda a Diachasmimorpha longicaudata (Ashmead) como otro posible agente para el control biologico de A. obliqua. Los parasitoides por si solos, probablemente no alcancen niveles economicos de control, pero pueden servir como componentes de un programa de manejo integrado de plagas para mantener zonas de exportacion de frutas libres o de baja prevalencia de moscas.

Translation provided by the authors.
Article Type: Report
Subject: Fruit-flies (Environmental aspects)
Parasitoids (Environmental aspects)
Pests (Biological control)
Pests (Methods)
Pests (Integrated control)
Agricultural pests
Authors: Serra, Colmar A.
Ferreira, Mileida
Garcia, Socorro
Santana, Loeny
Castillo, Maira
Nolasco, Caridad
Morales, Paula
Holler, Timothy
Roda, Amy
Aluja, Martin
Sivinski, John
Pub Date: 12/01/2011
Publication: Name: Florida Entomologist Publisher: Florida Entomological Society Audience: Academic Format: Magazine/Journal Subject: Biological sciences Copyright: COPYRIGHT 2011 Florida Entomological Society ISSN: 0015-4040
Issue: Date: Dec, 2011 Source Volume: 94 Source Issue: 4
Geographic: Geographic Scope: Dominican Republic Geographic Code: 5DOMN Dominican Republic
Accession Number: 298614295
Full Text: Neotropical and subtropical tephritid fruit flies infest hundreds of fruit and vegetable species (White & Elson-Harris 1992; Foote et al. 1993). Several polyphagous species are particularly destructive and responsible for trade restrictions wherever they occur (Siebert 1999; Siebert & Cooper 1995). Anastrepha obliqua (Macquart), the West Indian or Mango fruit fly, is one of the foremost of these pests and most frequently infests species of Anacardiaceae (Hernandez-Ortiz and Aluja 1993). Spondias spp. ("tropical plums") are particularly favored among native plants, but mango (Mangifera indica L.) is economically the most important host. Widespread, the fly occurs from the Greater (including Hispaniola) and Lesser Antilles to Mexico and south through Ecuador and parts of Brazil (Stone 1942; Foote et al. 1993). Wherever it exists, A. obliqua threatens both mangoes grown for local consumption, and complicates or precludes mango exports. Population levels in the Dominican Republic can be extremely high. For instance, up to 60 flies per trap have been captured in a single day in the mango orchards of Hato Damas (Serra et al. 2005a; Ogando & Serra 2006; Thomas et al. 2008). These high levels may be due to both a lack of sanitation measures and a depauperate natural enemy guild (Ovruski et al. 2000; Castillo et al. 2006).

The natural enemies of A. obliqua in Mexico have been investigated in detail (Sivinski et al. 1997, 1998; Aluja et al. 1998; Lopez et al. 1999), and 2 largely sympatric species of opiine braconids, Utetes anastrephae (Viereck) and Doryctobracon areolatus (Szepligeti), inflict high levels of mortality on A. obliqua in Spondias spp. Both U. anastrephae and D. areolatus attack late-instar Anastrepha spp larvae, but because of a significantly shorter ovipositor, U. anastrephae is only efficient at reaching hosts in small fruit (Sivinski et al. 1998, 2001). Doryctobracon areolatus on the other hand is a major natural enemy of a variety of Anastrepha spp. larvae in a large number of fruit. In Florida, where biological control introductions have reunited the two species, only D. areolatus is found in Psidium guajava L. but both species occur in the much smaller Eugenia uniflora (Sivinski et al. 1998). Even within a fruit species the mean size of fruit containing U. anastrephae can be smaller than that of fruits containing D. areolatus. In spite of its shorter ovipositor, limited host range, lower fecundity and shorter adult life span (Sivinski et al. 2000), U. anastrephae, appears to persist because of its superior ability as an "intrinsic competitor" in instances of multiparasitism (Aluja et al., unpublished data).

Utetes anastrephae, but not D. areolatus, historically has parasitized native Anastrepha spp. on Hispaniola and occasionally parasitizes up to 90% of A. obliqua locally in Spondias spp. (Serra et al. 2005b). Because the two species co-occur commonly on the American mainland, it was predicted that 1) D. areolatus would find the Dominican environment suitable, as does U. anastrephae; and 2) there would be no negative interactions between 2 closely co-evolved species; and overall parasitism would increase with the introduction of D. areolatus, particularly among flies developing in larger fruits.

Two regions of the Dominican Republic were chosen for parasitoid releases: Hato Damas in the southern part of the country and Mata Larga in the northeast. Evidence of D. areolatus recovery, offspring of released parasitoids collected in the same fruiting season, and of establishment (D. areolatus collected in a subsequent fruiting season), are presented in the following. In addition, we discuss U. anastrephae parasitism, the effects of fruit size and host density on parasitism by both species and search for any indication of D. areolatus excluding U. anastrephae from hosts. The introduction of another opiine braconid species, Diachasmimorpha longicaudata (Ashmead), is considered and we argue that, in this particular case, sequential introductions might be more efficacious than simultaneous.

MATERIALS AND METHODS

Origin of Parasitoids

Doryctobracon areolatus were reared at the Instituto de Ecologia, Xalapa, Veracruz, Mexico on larvae of Anastrepha ludens. Details on the facilities, equipment and procedures are available in Aluja et al. (2009).

Release Sites

Parasitoids were periodically released at sites chosen on the basis of relatively high Anastrepha spp. densities and large numbers of Spondias spp., particularly S. mombin L. host trees in the Hato Damas area near San Cristobal (18[degrees]24'59.51"N: 70[degrees]06'27.98"W) and in the Mata Larga area, and the rural surroundings of San Francisco de Macoris (19[degrees]18'01.83"N: 70[degrees]15'15.33"W). At each site there were initially 20 host tree-release points.

Release Schedule

Twenty one D. areolatus releases were made at approximately weekly intervals over the period, 17 Jun to 15 Dec 2005. Mortality and sex ratio of newly arrived parasitoids were recorded. They were then provided with honey and water, held for a min of 24 h, and separated into lots of 20 individuals (ca. 1 male: 2 females) each for transport to release sites. In total, 16,973 D. areolatus, 58% of them female, were taken into the field. Of these, 87% (14,79l) were released in the Hato Damas region. Five releases totaling 2,182 (67% female) insects were made in the Mata Larga region from 22 Jul to 30 Sep 2005.

Fruit Sampling and Parasitoid Recovery

Freshly fallen fruit and fruit from the canopy--when fallen fruits were absent--were collected, counted and weighed on the day of release, 2 days after and ~1 week after release. Sample sizes were based on estimates of available fruit (Sivinski et al. 1996; Sivinski et al. 1998). Larvae were allowed to emerge from fruit for a minimum of 10 d. They were then transferred to cups containing moistened sand as a pupation medium and held for another mo. Adult insect eclosion was noted over this period and insect identities were confirmed.

Statistical Analysis

With the most extensive data sets (insects from S. mombin; 2005, release year and 2007, a post-release year), the General Linear Models (GLM) procedure of the Statistical Analysis System (SAS Inst. 2004) was used to examine the following effects on parasitism by U. anastrephae and D. areolatus; estimated fruit size (= sample weight/number of fruit in the sample), mean numbers of hosts in the sample, mean parasitoid density (numbers of parasitoids/weight of fruit), and parasitism by the other parasitoid species. Parasitism data, being proportional, was log-arcsine transformed prior to analysis. Separate analyses were used to examine the effects of the following abiotic parameters on parasitism by both species: sample site (a class variable), Julian date and the quadratic of Julian date (to examine any possible non-linear relationships). In order to determine if parasitism by D. areolatus supplanted that of U. anastrephae, a Student t-test, with a Satterthwaite correction due to unequal variance, compared fruit samples that contained U. anastrephae and in which D. areolatus were either present or not. Lower mean parasitism by U. anastrepahae in the presence of D. areolatus could indicate competition for hosts, but similar levels of U. anastrephae parasitism in the 2 categories would suggest that D. areolatus was providing additional parasitism.

RESULTS

Evidence of Establishment and Spread of Doryctobracon areolatus

In 2007, 2 years following parasitoid releases, D. areolatus was recovered from 17 of 18 of the monitored localities in the Hato Damas region. Where parasitism occurred, percent parasitism ranged from l.l to 100% (Fig. l, derived from 18 Spondias spp. trees). In addition to being collected from S. mombin, D. areolatus was also collected from Anastrepha spp. in "tropical plum/ciruela" (S. purpurea L. var. 'flava' and var. 'purpurea', Anacardiaceae), golden apple/manzana de oro (S. cytherea Sonn., Anacardiaceae), guava/ guayaba (Psidium guajava L., Myrtaceae), Malay apple/manzana malaya (Syzygium malaccense (L.) Merril & Perry, Myrtaceae), bilimbi/vinagrillo (Averrhoa bilimbi L., Oxalidaceae), carambola (A. carambola L., Oxalidaceae), and tropical almond/ almendro tropical (Terminalia catappa L., Combretaceae). In the Mata Larga area establishment was finally confirmed by 2007 in collections of S. mombin (Table l), although parasitism was typically less than 10%. This relatively low level may have been due to the lower number of released parasitoids and fewer alternative fruit fly hosts.

Following post-release collections at release sites in 2007, additional fruits were collected in 2007-2008 at distances of 2.5 to 50 km from the nearest point of release. Doryctobracon areolatus was obtained from S. mombin, S. purpurea, A. carambola and P. guajava (Table 2; Fig. 2). The farthest of these points was in a commercial guava (cv. 'Cubano') orchard located in Piedra Blanca, Monsenor Nouel province, 50 km north-east of the nearest release site in the Hato Damas area. We have no way of knowing if the parasitoid dispersed there on its own or was carried by humans. Additional data on emergence of fruit flies and parasitoids during a 3.5-mo period in 2008 are presented in Fig. 2. Besides one specimen of U. anastrephae, all recovered parasitoids were D. areolatus, which attacked up to 60% of the available hosts.

[FIGURE 1 OMITTED]

Effects of Biotic and Abiotic Variables and of Potential Competition on Parasitism

In 2005, during D. areolatus releases, 129 samples of S. mombin taken from 20 sites yielded 2958 fruits (mean = 22.9 [stderr = 1.4]) weighing a total of 26.8 kg (mean = 207.1 g [15.5]) and producing 16,074Anastrepha sp. pupae, probably all A. obliqua (mean = 124.6 [11.0]). In 2007, a year following D. areolatus releases, 85 samples of S. mombin taken from 20 sites yielded 1625 pieces of fruit (mean = 19.1 [stderr = l.l]) weighing a total of 16.3 kg (mean = 192 g [15.0]) and producing 4274 Anastrepha sp. pupae, probably all A. obliqua (mean = 50.3 [5.9]).

In 2005, mean parasitism (# parasitoid [sp..sub.1]/ # parasitoid [sp..sub.1] + # parasitoid [sp..sub.2] + # adult A. obliqua) by U. anastrephae was 0.34 (0.02), and 0.09 (0.01) by D. areolatus. In 2007, mean parasitism by U. anastrephae was 0.18 (0.02) and by D. areolatus 0.13 (0.02). Among sites, parasitism by U. anastrephae ranged from 0-1.0 in 2005 and from 0-0.90 in 2007. Among sites/dates, parasitism by D. areolatus ranged from 0-1.0 in 2005 and from 0-0.75 in 2007.

The following pertains only to insects obtained from S. mombin collected in 2005 (release year) and 2007 (2 years post-release). In 2005, during D. areolatus releases, parasitism by U. anastrephae was significantly and negatively related to mean estimated fruit size (F = 5.5, df = l, P < 0.02). Parasitism by D. areolatus was not influenced by fruit size nor by host density or parasitism by U. anastrephae (F = 1.63, dfmodel = 7, dferror = 121, P = 0.13). It was subject to the effects of release sites (F = 2.0, df = 12, P = 0.03) and the interaction between release site and Julian date (F = 2.1, df = 12, P = 0.03). In 2007, subsequent to D. areolatus releases, there were no effects of fruit size, host density or parasitism by a competitor on either species (F D. areolatus = l.l, dfmodel = 7, dferror = 77, P = 0.40; F U. anastrephae = 1.0, dfmodel = 7, dferror = 77, p = 0.46). Parasitism by U. anastrephae was affected by sample site (F = 2.2, df = l, P < 0.02) and that by D. areolatus by Julian date (F = 11.3, df = l, P < 0.002).

There was no evidence that D. areolatus excluded U. anastrephae from hosts during either year. In 2005 and 2007, there were no differences in U. anastrephae parasitism in samples with and without D. areolatus (t(2005) = 1.0, df = 66.8, P = 0.32; t(2007) = 1.4, df = 61, P = 0.15).

DISCUSSION

Doryctobracon areolatus emerged from the puparia of A. obliqua following their release in the vicinity of fruiting S. mombin, S. purpurea, and P. guajava (infested with A. suspensa) and gave evidence of establishment when it was recovered from these same sites 2 years after releases had been concluded. Its ultimate distribution, density and capacity to control A. obliqua remain to be determined. This may not be the end of biological control efforts. Another candidate opiine parasitoid, Diachasmimorpha longicaudata (Ashmead), was not immediately released. It is an Indo-Malaysian exotic that has been introduced worldwide for tephritid control, and is a particularly effective natural enemy of Anastrepha suspensa (Loew) (sivinski et al. 1996) We were concerned that it might suppress a critical alternative host for D. areolatus and so we postponed its establishment.

If D. longicaudata is also released the range of D. areolatus may shrink. In Mexico, D. longicaudata is more abundant than D. areolatus at higher altitudes (sivinski et al. 2000) and in larger, commercial fruits (Lopez et al. 1999). It is unclear if the altitudinal distributions are the result of interspecific competition leading to habitat subdivision, but in Florida where first D. areolatus and then D. longicaudata was introduced to control A. suspensa, there is evidence of displacement (Eitam et al. 2004). Both species were originally established in southern Florida, but at present D. areolatus occurs in the northern portion of the peninsula (in spite of being more abundant at lower, warmer altitudes in Mexico) and D. longicaudata occurs in the southern portion with only a narrow range of overlap. One explanation for this distribution is that D. areolatus is better able to persist during periods of host scarcity and in areas with lower host-plant diversity. Thus the northern part of A. suspensa's range provides a refuge from an otherwise superior competitor. In terms of biological control, parasitism levels were not noticeably affected by the replacement of one species by the other (Baranowski et al. 1993). There appears to be little reason for concern about the effects of D. longicaudata on the endemic U. anastrephae. It is widespread in Florida and occurs in the ranges of both introduced species (Eitam et al. 2004).

The possible effects of D. areolatus, a parasitoid with a broad host range within the genus Anastrepha, on native, non-target tephritids was also considered by the Ministry of Agriculture prior to release. In addition to obliqua and suspensa another 5 species of Anastrepha occur on Hispaniola: A. dissimilis Stone, A. insulae Stone, A. ocresia Walker, A. antillensis Norrbom and A. stonei Steyskal (Stone 1942; Norrbom 1998). While there was no guarantee that D. areolatus would not attack these species as well, typically D. areolatus parasitism rates of uncommon, nonpestiferous flies are very low (< 1%; e.g., Aluja et al. 2000; Aluja et al. 2003; Pereira et al. 2007; Rull et al. 2009).

[FIGURE 2 OMITTED]

Biological control, even with the addition of D. areolatus, is unlikely to unilaterally solve the economic problems created by A. obliqua. However, it could serve as a component of an integrated pest management program designed to protect "flyfree export" or "low-prevalence" zones, particu larly if high fly populations in non-commercial Spondias spp. could be suppressed leaving fewer flies to disperse into agricultural environments (Sivinski et al. 1996).

ACKNOWLEDGMENTS

We thank Dr. Robert Wharton, Department of Entomology, Texas A&M University who originally identified the parasitoids. Caroline Cohen USDA, APHISIS provided essential funding. Invaluable technical assistance was provided by Daniel Virgil, Eugenio Rodriguez, Jose Asiatico, Pedro Marte, Raul Nina, Jose Volquez (all DSV-MA), Xiomara Cayetano, Teofila Reinoso (IDIAF-CENTA), Lucia Silverio, Juan de Dios Moya, Jose Luis Gonzalez y Luis Antonio Cabrera (IDIAF-EEML). Portions of this work were financially supported by INECOL, and by grants to MA from the Mexican Consejo Nacional de Ciencia y Tecnologia (CONACyT Grant No. 46846-Q) and the Mexican Campana Nacional contra Moscas de la Fruta (Secretaria de Agricultura, Ganaderia, Desarrollo Rural y PescaInstituto Interamericano de Cooperacion para la Agricultura (SAGARPA-IICA).

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COLMAR A. SERRA (1), MILEIDA FERREIRA (1), SOCORRO GARCIA (1), LOENY SANTANA (1), MAIRA CASTILLO (2), CARIDAD NOLASCO (3), PAULA MORALES (4), TIMOTHY HOLLER (5), AMY RODA (6), MARTIN ALUJA (7) AND JOHN SIVINSKI (8)

(1) Institute Dominicano de Investigaciones Agropecuarias y Forestales (IDIAF) Santo Domingo, Republica Dominicana

(2) Universidad Autonoma de Santo Domingo (UASD), Santo Domingo, Republica Dominicana

(3) Depto. de Sanidad Vegetal-Ministerio de Agricultura (DSV-MA), Santo Domingo, Republica Dominicana

(4) USDA-APHIS-IS, Ave. Pedro Henrfquez Urena, #133--La Esperilla, Santo Domingo, Dominican Republic

(5) USDA-APHIS (ret.) at Center for Medical, Agricultural and Veterinary Entomology, 1600 SW 23rd Dr., Gainesville, FL 32608

(6) USDA-APHIS, Subtropical Horticultural Research Station. Miami, FL 33125

(7) Instituto de Ecologia, A.C., Apartado Postal 63, 91000 Xalapa, Veracruz, Mexico

(8) USDA-ARS, Center for Medical, Agricultural and Veterinary Entomology, 1600 SW 23rd Dr., Gainesville, FL 32608
TABLE 1. RECOVERY OF DORYCTOBRACON AREOLATUS FROM ANASTREPHA
OBLIQUA INFESTING SPONDIAS MOMBIN FRUITS COLLECTED IN THE MATA
LARGA AREA IN 2007.

                                 % of emerged insects

Tree #   Date   Pupae      D.         U.       Anastrepha
                        areolatus  anastrephae

2        21/8    70       1.4        11.4        87.1
3        21/8    39       2.6        15.4        82.1
4        21/8    65       3.1         0.0        96.9
4         3/9    32       9.4         6.3        84.4
9         3/9    69       6.3        25.0        68.8
9        26/9    32       5.0         0.0        95.0
10       26/9    24       6.0         0.0        94.0
12       21/8    44       4.5         4.5        90.9
15       21/8    83       7.3         0.0        92.7

         % of emerged
           insects

Tree #    Parasitism

2            12.9
3            17.9
4             3.1
4            15.6
9            31.3
9             5.0
10            6.0
12            9.1
15            7.3

TABLE 2. COLLECTIONS OF FRUIT FROM NON-RELEASE SITES IN 2007-8
THAT YIELDED DOEYCTOBEACON AEEOLATUS. LOCATION REFERS TO THE
DISTANCE (KM) AND DIRECTION FROM THE NEAREST RELEASE POINT.

                   Where     Date    Number   Weight   Pupae/   #
                 fruit was             of       of      kg     pupae
                 collected           fruit    fruits
                  km and
                 direction
                   from
Site, Host        nearest
                  release
                   site

La Cruz            3,SW      21/08     25      155       97     15
  B, S. mombin
La Cruz            6,SW      40918     25      198      250     40
  D, S. mombin
Los Cocos,        2.5,SE     40977     85      335      314     85
  S. mombin
Los Mameyes,      4.5,SE     21/08     16      400      100     40
  S. purpurea
Feliciano,        5.5,SE     21/08     20      155      452     70
  S. mombin
La Pared,          7,SE      21/08     20      240      146     35
  S. mombin
Piedra Blanca,     50,NW     18/10     1       300       83     25
  P. guajava

                                    % Emergence

Site, Host     Anastrepha     D.          U.       Parasitism
                           Areolatus  Anastrepahae

La Cruz           68.0        4.0        28.0        32.0
  B, S. mombin
La Cruz          100.0        0.0         0.30        0.0
  D, S. mombin
Los Cocos,        45.9        2.4        51.8        54.1
  S. mombin
Los Mameyes,      90.0       10.0         0.0        10.0
  S. purpurea
Feliciano,        78.6        8.6        12.9        21.4
  S. mombin
La Pared,         94.3        0.0         5.7         5.7
  S. mombin
Piedra Blanca,    72.0       28.0         0.0        28.0
  P. guajava
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