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Parasaissetia nigra (Hemiptera: Coccidae) and its parasitoids from the genus Coccophagus (Hymenoptera: Aphelinidae), with description of a new species from Tamaulipas, Mexico.

Soft scales of the family Coccidae (Hemiptera: Coccoidea) are phytophagous insects that infest leaves, branches and fruits of various plants. Some species are pests of agricultural crops, for example, Saissetia oleae Olivier and Coccus hesperidum L. (Hayat 1997; Stauffer & Roaw 1997). On the other hand, they are host for parasitic wasps that belong predominantly to 9 genera of Chalcidoidea. Among these, species of 4 genera, including Coccophagus Westwood, are primary endoparasitoids and have economic importance for biocontrol of hemipteran pests (Hayat 1998).

Parasaissetia nigra (Nietner) belongs to the family Coccidae and has worldwide distribution (Noyes 2012a). It was described by Nietner in 1861 from Ceylon and has many synonyms and various combinations (Ben-Dov et al. 2013). Smith (1944) suggested that several strains of P. nigra may exist, each with different host preferences, or there may be several geographical races (De Lotto 1967). Hayat (1997) noted that the Afrotropical region is richer in Coccophagus species parasitizing P. nigra and also has more endemic species.

Parasaissetia nigra is polyphagous, feeding on host plants from 80 families (Ben-Dov 1993), especially on ornamental plants of tropical origin. Several agricultural crops are attacked, including avocado, citrus, coffee, cotton, guava, mango, pomegranate and other plants. Scales often infest heavily leaves, branches and fruits (Clausen 1978; Hamon & Williams 1984).

These scales produce copious, sticky honeydew on which sooty moulds develop, coating the plant. This restricts photosynthesis, weakening the plant and sometimes stunning new growth and causing defoliation (Smith 1944). Parasaissetia nigra is a moderate pest of ornamental plants, particularly in tropical countries. The scale is also a minor pest of citrus and of other agricultural crops and, at times, has been an important pest (Smith 1944).

In Mexico, this soft scale is widely distributed in the states of Baja California, Chihuahua, Colima, Guanajuato, Guerrero, Jalisco, Michoacan, Morelos, Nayarit, Nuevo Leon, Oaxaca, Puebla, Queretaro, Sinaloa and Sonora (Miller 1996). Parasaissetia nigra was newly recorded for the states of Tamaulipas and San Luis Potosi; in Tamaulipas it was collected in 2012, and according to our investigations, in San Luis Potosi it was found earlier (Myartseva 2006). Despite its wide distribution, polyphagy and economic importance as potential pest of agricultural crops, morphological and biological descriptions are lacking in the Mexican scientific literature. This article provides a morphological description of P. nigra and its parasitoids based in the literature and based on our own observations.

MATERIALS AND METHODS

Infested leaves and twigs with soft scales of several plants were found and examined in the field using a magnifying pocket lens (10X), and later transferred to the laboratory to be examined under a Leica MZ6 microscope (140X). Collection and rearing of parasitoids were carried out following methodologies by Noyes (1982). Leaves and twigs were placed separately in glass containers until emergence of parasitoids. For further examination and identification reared adult parasitoids were mounted on microscope slides with Canada balsam. The species of soft scale was identified by Dr. I. A. Gavrilov-Zimin, specialist in scale insects from the Zoological Institute of the Academy of Sciences of Russia, Saint Petersburg. All materials are preserved in the Insects Museum of the Universidad Autonoma de Tamaulipas, Mexico. This insect collection has 195 specimens of Coccophagus on slides and numerous specimens in 75% alcohol.

RESULTS AND DISCUSSION

Parasaissetia nigra (Nietner)

Adult female is elongate-oval, shiny, dark brown, 3-4 mm long. Body shape varies according to the substrate, specimens found on leaves are broad, only slightly convex but much more convex than those on stems or leaf-mid-ribs, which are elongate and less convex. Immature stages and young adult specimens of P. nigra are translucent-yellow and sometimes mottled (Hamon & Williams 1984).

In California and Florida, P. nigra has 1 complete generation per year outdoors (Gill 1988). Ben-Dov (1978) recorded up to 6 generations per year in greenhouses in Israel. In Tamaulipas, Mexico, from Oct 2012 to Jun 2013, we observed the development of at least 2 complete generations of P. nigra on mistletoe Phoradendron spp. (Santalales: Santalaceae) near Rio San Marcos in Ciudad Victoria. Upon hatching, the first instar nymphs (crawlers) move away from the female to other parts of the plant, where they fix themselves and start feeding.

It is interesting that in natural landscapes in Tamaulipas, scale colonies developed on mistletoes, hemiparasitic plants from the genus Phoradendron, but not on Acacia farnesiana (L.) Willd., Guazuma ulmifolia Lam., Salix humboldtiana Willd. and Prosopis glandulosa Torr., which have been reported as host plants of this species. In Mexico, P nigra was recorded as pest of guava (Ben-Dov 1978). Moreover, parasitoids were obtained only from P nigra on huisache Acacia farnesiana (L.) Willd. in the State of Tamaulipas.

Families of parasitoids of Parasaissetia nigra

Parasitoids from several families of Chalcidoidea have been reported as natural enemies of P nigra in the world: Encyrtidae, Aphelinidae, Eulophidae, Eupelmidae and Pteromalidae. In Peru, the dominant parasitoid species in agro-ecosystems belong to 3 families: Encyrtidae, Aphelinidae and Pteromalidae (Nunez 2008). In many countries where it was once a pest, P nigra is now successfully controlled by natural enemies originally introduced to control Saissetia oleae (Bartlett 1978). For example, the most effective control agent of P. nigra in California (USA), is an encyrtid Metaphycus helvolus (Compere), that was introduced with several other enemies to control S. oleae, which has been more effective against P. nigra (Ebeling 1959).

In Mexico, we reared from P. nigra parasitoids from 6 families: Encyrtidae, Aphelinidae, Eupelmidae, Eulophidae, Pteromalidae and Signiphoridae, but the encyrtid and aphelinid species were the most dominant. This is the first record of Signiphoridae as parasitoids of P. nigra. The main parasitoids in the family Aphelinidae are species of the genus Coccophagus Westwood.

Coccophagus spp.--parasitoids of Parasaissetia nigra

Species of the genus Coccophagus are mainly parasitoids of soft scales (Coccidae), but rarely parasitize armored scales (Diaspididae) and other Coccoidea. In the world, the genus Coccophagus consists of 257 species (Noyes 2012a), some of which are widely distributed. In the family Aphelinidae, Coccophagus is the second most speciose genus after Encarsia Foerster. Coccophagus is divided into 6 species-groups: lycimnia-group, pseudococci-group, varius-group, malthusi-group, ochraceus-group and zebratus-group (Hayat 1997).

Females of this genus have 8-segmented antenna; mandible with 1 or 2 teeth and a truncation; pronotum entire, medially sometimes narrow; mid lobe of mesoscutum with numerous short setae; axillae large, strongly projecting forwards, with at least 2 setae, rarely more to about as densely setose; Each side lobe with 4 or more setae, rarely less; scutellum large, usually convex, not overlapping propodeum, either with 3 pairs of setae or several additional setae to densely setose; propodeum either medially membranous or with a triangular median projection: fore wing large, broad, densely setose, with short marginal fringe; submarginal vein with 5 or more setae, stigma vein variable, either subsessile or with a neck and swollen stigma; linea calva absent; hind wing usually broad, with a broadly rounded apex; all tarsi 5-segmented; hind coxae sometimes large, as long as femora; tibiae often with thick setae (bristles) along dorsal (outer) margins; gaster with 7 terga; length of ovipositor and relative dimensions of last tergum highly variable; hypopygium extending to about two-thirds along gaster and with apex broadly rounded or truncate; color of body variable from whitish-yellow to brown black, partially or entirely; males similar to females except for genitalia and, in most species, antennae quite different from those of females.

Coccophagus females are diploid, developing from fertilized eggs, but are also produced from unfertilized eggs, whereas the males are invariably haploid, produced from unfertilized eggs; males are either primary ectoparasitoids, secondary ectoparasitoids or endoparasitoids of other primary hymenopterous parasitoids, including females of the same species (Hayat 1997). For example, females of C. caridei (Brethes) are soft scale parasitoids, but males develop in the mealybug Planococcus citri (Risso) as hyperparasitoids of the encyrtid Anagyrus pseudococci (Girault) (Flanders et al. 1961).

Twenty-four species of Coccophagus have been recorded as parasitoids of P. nigra, and of these some species have a worldwide in distribution due to various introduction programs (Hayat 1997; Noyes

2012a). An analysis of the lists of species distributed in some large regions--South Africa, Oriental and Neotropical, and United States according to Noyes (2012a), showed that these regions have a similar number of Coccophagus species that parasitize P. nigra: In addition to the widespread parasitoid species some regions have 1-2 specific parasitoids from their local fauna: South Africa--1 from a total of 12 species, the Oriental Region--1 of 8 species, and the Neotropical Region--2 of13 species (Table 1). In the South Africa list, some species of Coccophagus were included by Hayat (1997): C. bivittatus Compere, C. lutescens Compere, C. modestus Silvestri, C. nubes Compere, C. saintbeauvei Compere and C. varius Silvestri.

In Tamaulipas, Mexico, we reared the following 5 Coccophagus species from P. nigra: C. rusti Compere (introduced into Mexico accidentally from California, where it was introduced for Saissetia oleae), C. lycimnia (Walker), C. ochraceus Howard, C. minor sp. nov. and Coccophagus sp. As Table 1 shows, 2 other species of Coccophagus (C. pulvinariae and C. scutellaris) are widely distributed in the world; in Mexico, they are parasitoids of other coccid species: C. lycimnia from Philephedra lutea (Cockerell), Coccus hesperidum L., Pulvinaria spp. and Saissetia spp. (Myartseva et al. 2012).

Below is presented a key to species of Coccophagus associated with P. nigra in Mexico, including C. scutellaris and C. pulvinariae, species present in Mexico as parasitoid, of other soft scales that probably also attack P. nigra. AH these species are distributed in the Neotropical Region and USA (California).

Key to Species of Coccophagus associated with P. nigra in Mexico

1a. Scutellum with 3 pairs of setae

1b. Scutellum with numerous scattered setae. Scutellum yellow, fore and mid femora yellow, hind femora black

scutellaris (Dalman)

2a. Fore wing distinctly or slightly infuscate

2b. Fore wing hyaline

3a. Scutellum yellow, at most the anterior margin narrowly blackish. Legs yellow, mid and hind coxae infuscate basally

pulvinariae Compere

3b. Scutellum dark brown. Propodeum light yellow. Hind coxae, trochanters and femora light yellow

rusti Compere

4a. Antennae with funicle segments ventrally connected

4b. Antennae with funicle segments centrally connected

5a. Body primarily yellow with black to dark brown pronotum medially, mesoscutum anteriorly, propodeum and band on apical half of gaster. Antennal scape longer than funicle, club shorter than funicle

ochraceus Howard

5b. Body completely yellow. Antennal scape as long as funicle, club as long as funicle.

minor Myartseva sp. nov.

6a. Antennal scape and pedicel infuscate. Hind tibia blackish

lycimnia (Walker)

6b. Antennal scape and pedicel light yellow. Hind tibia light yellow

Coccophagus sp.

COCCOPHAGUS MINOR MYARTSEVA, SP. NOV. (Figs. 1-4)

Type Material

HOLOTYPE female, MEXICO, Tamaulipas, Ciudad Victoria, Rio San Marcos, ex Parasaissetia nigra (Nietner) on Phoradendron quadrangulare (Kunth) Griseb., associated with Acacia farnesiana (L.) Willd., 18.IV.2013 (col. E. RuizCancino, N. Y. Martinez-Ruiz, B. Villarreal-AIanis, N. Rivera-Tovias). Paratype: same locality and host, 12, 18.IV.2013 (col. E. Ruiz-Cancino, N. Y. Martinez-Ruiz, B. Villarreal-Alanis, N. RiveraTovias). Both specimens mounted in slides. Holotype deposited at the Entomological Research Museum, University of California--Riverside, USA, paratype deposited in UAT Museum.

Description

Length of body--0.7 mm. Coloration. Head light yellow, face whitish, second-sixth flagellar segments slightly infuscate; low border of cheeks, near mouth margin, black, eyes and ocelli reddish. Body light yellow, apex of third valvulae slightly infuscate. Fore wings hyaline. Legs whitish yellow.

Structure. Head not wider than thorax, about 1.3 times as wide as high. Frontovertex 0.5 times as wide as head width. Distance between posterior ocelli 1.8 times as long as distance from hind ocellus to eye margin. Eyes 0.8 times as long as cheeks. Mandible with 1 tooth and a truncation. Antennae (Fig. 1) inserted below the level of lower margin of eyes, closer to mouth margin. Distance between toruli 0.6 times as long as distance from torulus to eye. Antennal radicle short, as wide as long. Scape about 6.4 times as long as wide. Pedicel 1.9 times as long as wide. First segment of funicle (F1) shorter than pedicel and about 2 times as long as wide. Second segment (F2) the longest and also 2 times as long as wide. Third segment (F3) as wide as second segment and 1.7 times as long as wide. Pedicel and funicle furnished with sparse, large setae. Club 1.3 times wider than funicle and as long as funicle. Secondsixth segments (F2-F6) of flagellum with 1 long sensilla each. Segments of funicle ventrally connected, longer ventrally than dorsally. Mid lobe of mesoscutum with sparse, large setae, 2 basal setae longer. Axilla large, with 2 long setae. Side lobe with 3 long setae. Scutellum about 0.8 times as long as mid lobe, with 3 pairs of long setae situated symmetrically. Fore wing uniformly setose, 2.7 times as long as maximum width of disc. Marginal vein slightly longer than submarginal vein. Stigmal vein (Fig. 2) short, with wide uncus. Marginal fringe about 0.2 times as long as wing width. Hind wing about 7 times as long as maximum width of wing, its marginal fringe about 0.8 times as long as wing width. All tarsi 5-segmented. Mid tibial spur (Fig. 3) longer than basitarsus of mid leg (25:20). Gastral tergites T2-T7 with 2, 2, 2, 4, 6 and 4 setae. Ovipositor (Fig. 4) slightly exserted, about as long as mid tibia. Third valvula about 0.3 times as long as second valvifer and about as long as basitarsus of mid leg.

[FIGURES 1-4 OMITTED]

Male unknown.

Remarks

Coccophagus minor sp. nov. belongs to the ochraceus species-group. The new species is close to C. lutescens Compere described from South Africa and to C. perflavus Girault described from United States. We compared C. minor with the original descriptions and redescriptions of both species (Girault 1916; Compere 1931; Annecke & Insley 1974; Hayat 1998). Both species are small in size, with the head and body pale yellow, without any dark markings. Coccophagus minor has slightly infuscate antenna and apex of third valvula, and black low border of cheeks near mouth margin. Structural differences are in Table 2.

Caption: Figs. 1-4. Coccophagus minor sp. nov., female: 1 antenna, 2--stigmal vein, 3--mid tarsus and mid tibial spur, 4 - ovipositor.

ACKNOWLEDGMENTS

Authors are thankful to I. A. Gavrilov-Zimin (Zoological Institute, Russian Academy of Sciences) for the identification of soft scale, and to project "Muerdagos de Ciudad Victoria, Tamaulipas, Mexico. Etapa 1" from Universidad Autonoma de Tamaulipas for its support. Also to Jacinto TreviNo-Carreon and Arturo Mora-Olivo for the identification of mistletoes and host plants, and to Nabil Yessenia Martinez-Ruiz, Brenda Villarreal-Alanis, Naylea Rivera-Tovias and Samuel Mireles-Cepeda (Facultad de IngenierIa y Ciencias, UAT) for their help in the collections of mistletoes and soft scales in Victoria, Tamaulipas, Mexico. We thank the reviewers and the associate editor of Florida Entomologist for their excellent suggestions.

REFERENCES CITED

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BARTLETT, B. R. 1978. Coccidae, pp. 57-74 In C. P. Clausen [ed.], Introduced parasites and predators of arthropod pests and weeds: A world review. U.S. Dept. Agric., Agric. Handbook No. 480. 545 pp.

BEN-DOV, Y. 1978. Taxonomy of the nigra scale Parasaissetia nigra (Nietner) (Homoptera: Coccoidea: Coccidae), with observations on mass rearing and parasites of an Israeli strain. Phytoparasitica 6: 115127.

BEN-DOV, Y. 1993. A systematic catalogue of the soft scale insects of the world (Homoptera: Coccoidea: Coccidae) with data on geographical distribution, host plants, biology and economic importance. Flora & Fauna Handbook No. 9. Sandhill Crane Press, Gainesville, Florida. 536 pp.

BEN-DOV, Y., MILLER, D. R., AND GIBSON, G. A. P. 2010. ScaleNet: a database of the scale insects of the 282 world. Available from: http://www.sel.barc.usda.gov/ scalenet/scalenet.htm (Access: March 2013).

CLAUSEN, C. P. 1978. Introduced parasites and predators of arthropod pests and weeds: a world review. USDAARS Agric. Handbook No. 480. 545 pp.

COMPERE, H. 1931. A revision of the species of Coccophagus, a genus of hymenopterous, coccid-inhabiting parasites. Proc. U.S. Nat. Hist. Mus. 78(7): 1-132.

DE LOTTO, G. 1967. The soft scales (Homoptera: Coccidae) of South Africa. I. South African J. Agr. Sci. 10: 781-810.

EBELING, W. 1959. Subtropical fruit pests. University of California, Div. Agric. Sci., Berkeley, California, U.S.A. 436 pp.

FLANDERS, S. E., BARTLETT, B. R., AND FISHER, T. W. 1961. Coccophagus basalis (Hymenoptera: Aphelinidae): its introduction into California with studies of its biology. Ann. Entomol. Soc. America 54: 227237.

GILL, R. J. 1988. The scale insects of California. Part I. The soft scales (Homoptera: Coccoidea: Coccidae). Tech. Serv. in Agric. Biosystematics and Plant Pathology, California Dept. Food and Agric. 1: 1-132.

GIRAULT, A. A. 1916. Notes on described chalcidoid Hymenoptera with new genera and species. Soc. Entomol., Stuttgart 31: 42-44.

HAMON, A. B., AND WILLIAMS, M. L. 1984. The soft scale insects of Florida (Homoptera: Coccoidea: Coccidae). Arthropods of Florida and neighboring land areas, vol. 11. Gainesville, Florida, U.S.A. 94 pp.

HAYAT, M. 1997. Aphelinidae, pp. 111-145 In Y. Ben-Dov and C. J. Hodgson [eds.], Soft scale insects--Their biology, natural enemies and control. Vol. 7B. Elsevier Science B.V.

HAYAT, M. 1998. Aphelinidae of India (Hymenoptera: Chalcidoidea): a taxonomic revision. Mem. on Entomol., Intl. Assoc. Publ., Gainesville, Florida, U.S.A. 13: 1-416.

MILLER, D. R. 1996. Checklist of the scale insects (Coccoidea: Homoptera) of Mexico. Proc. Entomol. Soc. Washington 98(1): 68-86.

MYARTSEVA, S. N. 2006. Review of Mexican species of Coccophagus Westwood, with a key and description of new species (Hymenoptera: Chalcidoidea: Aphelinidae). Zoosystematica Rossica 15(1): 113-130.

MYARTSEVA, S. N., RUIZ-CANCINO E., AND CORONADOBLANCO, J. M. 2012. Aphelinidae (Hymenoptera: Chalcidoidea) de importancia agrIcola en Mexico. Revision y claves. Serie Avispas parasIticas de plagas y otros insectos, N 8. UAT, FIC, Mexico. 413 pp. Printed en CD.

NIETNER, J. 1861. In: Observations on the enemies of the coffee tree in Ceylon. Ceylon Times, Ceylon. 31 pp.

NOYES, J. S. 1982. Collecting and preserving chalcid wasps (Hymenoptera: Chalcidoidea). J. Nat. Hist. 16: 315-334.

NOYES, J. S. 2012a. Universal Chalcidoidea Database [online]. Worldwide Web electronic publication. www. nhm.ac.uk/entomology/chalcidoids/index.html. (Last updated: June 2012).

NOYES, J. S. 2012b. An inordinate fondness of beetles, but seemingly even more fond of microhymenoptera! Hamuli. The Nwsl. Intl. Soc. Hymenopterists 3: 5-8.

NUNEZ, E. 2008. Plagas de paltos y cItricos en Peru, pp. 324-364 In R. Ripa and P. Barral [eds.], Manejo de plagas en paltos y cItricos (un estudio de lujo para el agro nacional). 390 pp.

SMITH, R. H. 1944. Bionomics and control of the nigra scale, Saissetia nigra. Hilgardia, 16: 225-288.

STAUFFER, S., and Rose, M. 1997. Biological control of soft scale insects in interior plantscapes in the USA, pp. 183-225 In Y. Ben-Dov, and C. J. Hodgson [eds]. Soft scale insects--Their biology, natural enemies and control. Vol. 7B. Elsevier Science B.V. 442 pp.

SVETLANA NIKOLAEVNA MYARTSEVA, ENRIQUE RUIZ-CANCINO AND JUANA MARIA CORONADO-BLANCO *

Facultad de Ingenieria y Ciencias, Universidad Autonoma de Tamaulipas, 87149 Cd. Victoria, Tamaulipas, Mexico

* Corresponding author; E-mail: jmcoronado@uat.edu.mx
TABLE 1. COCCOPHAGUS PARASITOIDS OF PARASAISSETIA NIGRA AND THEIR
DISTRIBUTION IN THE WORLD (AFTER NOYES 2012A).

Species of Coccophagus    SA1   USA   Oriental   Neotropical   Mexico

C. basalis Compere         +     +                    +
C. bogoriensis                           +            +
  (Koningberger)
C. capensis Compere        +     +                    +
C. caridei (Brethes)             +                    +
C. ceroplastae             +     +       +            +
  (Howard)
C. cooperatus                            +
  Sugonjaev & Ren
C. cowperi Girault         +     +       +            +
C. fallax Compere                                     +
C. hawaiiensis             +     +       +            +
  Timberlake
C. isipingoensis           +
  Compere
C. lycimnia (Walker)       +     +       +            +          +
C. minor Myartseva                                               +
  sp. nov.
C. ochraceus Howard        +     +       +            +          +
C. pulvinariae Compere     +     +                    +          +
C. rusti Compere           +     +                    +          +
C. saissetiae Gahan                                   +
C. scutellaris (Dalman)    +     +                    +          +
C. sp.                                                           +

LSA = South Africa, USA = United States of America.

TABLE 2. STRUCTURAL DIFFERENCES OF THREE COCCOPHAGUS SPECIES.

Structures        C. lutescens Compere      C. perflavus Girault

Pedicel          1.5 times as long as      more than 1.5 times
                   wide and 1.5 times as     as long as wide and
                   long as F1                about equal to F1
F1               1.25 times as long as     slightly more than 2
                   wide                      times as long as wide
F1-F2            F2 and F1 subequal in     F2 1.3 times as long
                   length                    as F1
F2-F3            slightly longer than      about 2 times as long
                   wide                      as wide
Mid tibial spur  slightly longer than      as long as basitarsus
                   basitarsus
Ovipositor       at least slightly         distinctly shorter
                   longer than mid tibia     than mid tibia
Length of body   0.6 mm                    0.8 mm

Structures          C. minor sp. nov.

Pedicel          1.9 times as long as
                   wide and slightly
                   longer than F1
F1               about 2 times as long
                   as wide
F1-F2            F2 1.5 times as long
                   as F1
F2-F3            F2 twice, F3 1.7
                   times as long as wide
Mid tibial spur  1.3 times as long as
                   basitarsus
Ovipositor       as long as mid tibia

Length of body   0.7 mm
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Author:Myartseva, Svetlana Nikolaevna; Ruiz-Cancino, Enrique; Coronado-Blanco, Juana Maria
Publication:Florida Entomologist
Article Type:Report
Geographic Code:1MEX
Date:Sep 1, 2014
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