PROC. ENTOMOL. SOC. WASH. 106(2), 2004, pp. 352-360 A REVIEW OF THE GENUS DOIRANIA WATERSTON (HYMENOPTERA: TRICHOGRAMMATIDAE), WITH A DESCRIPTION OF A NEW SPECIES FROM NORTH AMERICA John D. Pinto CA Department of Entomology, University of California, Riverside, 92521, U.S.A. (e- mail: [email protected]) — Abstract. The trichogrammatid genus Doirania is reviewed. The genus, previously known only from species in Japan and New Guinea, has a considerably more widespread distribution which includes North America and other areas of the Palaearctic. Three spe- cies are assigned. The North American species {D. elegans, n. sp.) is described and compared to congeners. The limits of Doirania and its relationship to other members of the tribe Oligositini are discussed. Key Words: Hymenoptera, Trichogrammatidae, Doirania, taxonomy As is the case with most trichogrammatid pear to be closer to Doirania. The current genera, Doirania is uncommonly collected definition of Doirania is retained pending a and poorly known. It was described by Wa- complete evaluation of oligositine relation- terston (1928) for a single species, D. leef- ships. mansi, a parasite in eggs of Tettigoniidae Terminology employed for most morpho- (Orthoptera), from Ambon, Indonesia. A logical traits follows Doutt and Viggiani second species, D. longiclavata Yashiro, (1968) and Gibson (1989, 1997). Terms for from Japan, was added in 1980. Recent col- antennal sensilla follow Olson and Andow lections show the genus to be considerably (1993), and Pinto (1999). more widespread. This paper presents a Doirania Waterston brief review of the genus and the descrip- tion of an additional species, D. elegans, Doirania Waterston 1928: 386. Type spe- which is widespread in eastern North cies: Doirania leefmansi Waterston 1928, America. original designation. Doutt and Viggiani Doirania is assigned to the tribe Oligo- 1968: 499; Viggiani 1971: 208; Hayat sitini (Viggiani 1971). It has been consid- and Subba Rao 1985: 241, 304; Pinto 1997: 773. ered close to Oligosita (Doutt and Viggiani — 1968, Yashiro 1980), and possibly deserv- Diagnosis. Ranging from 0.4-0.8 mm ing only subgeneric status (Viggiani 1971). in length; color light to dark brown. Head: The primary feature separating the two gen- Foramen magnum near top of head, at or era historically is antennal club segmenta- above level of dorsal margin of eyes (Fig. tion (one in Doirania, two or three in Oli- 1). Antennal formula (Fig. 4): 2 anelli (2nd gosita). Although additional traits separat- anellus discoid, inconspicuous), funicle 1- ing these taxa are proposed here, generic segmented, club 1-segmented; funicle well limits remain questionable, and certain spe- separated from club, transverse; club with cies cuiTcntly assignable to Oligosita ap- 6 placoid sensilla (2 at middle and 4 api- VOLUME NUMBER 106, 2 353 cally), with at most 1 or 2 unsocketed setae, species of Epoligosita also have a one-seg- these at extreme base when present; length mented club (Doutt and Viggiani 1968) but of scape and pedicle combined greater than in that genus, as in other oligositines, the that of flagellum. Mesosoma: Finely etched foramen is placed near the middle of the longitudinal line present medially on scu- head (Fig. 2), much closer to the mouth- tum and scutellum (correlated with a white parts, and the metasomal terga are uniform, line visible in dried specimens). Mesopleu- lacking a striate posterior section. Chaetos- ron without a pleural suture. Venter of me- trichella, also with a one-segmented club sothorax with distinct transepisternal sulci (Doutt and Viggiani 1968, as Brochista), (see Gibson 1989). Forewing (Fig. 15) 2.5- has a more ventrally placed foramen mag- 3X as long as wide; longest fringe setae num, an elongate funicle, more complex length ca. Vi-^ greatest wing width. Meta- genitalia, and an ovipositor which extends soma: At least the anterior 3 terga longitu- considerably beyond the apex of the meta- dinally striate posteriorly (Figs. 13, 14). soma. Two or more metasomal sterna completely Doirania can be separated unambiguous- divided longitudinally and ovipositor short, ly from other described oligositine genera. not extending beyond apex of metasoma or Yet it is probable that certain undescribed only slightly so (Figs. 8, 9). Male with a species, currently assignable to OUgosita relatively broad, apically truncate ventro- based on antennal segmentation, are actu- medial projection on antepentultimate ster- ally closer to Doirania. Unfortunately, num (Fig. 10). Male genitalia simple, as in these taxa are known only from females several other oligositine genera, reduced to which makes their placement difficult at a single tube with two short apodemes at present. OUgosita is the largest genus of base (Figs. 1—0, 16. 17). Trichogrammatidae and it is likely that it is Remarks. The Oligositini are recog- composed of two or more unrelated line- nized by features of the male genitalia (Vig- ages which simply lack certain derived fea- A giani 1971) as well as by the black rather tures of other oligositine genera. detailed than red compound eyes and the presence analysis of the entire tribe is required before of one instead of two pair of setae each on generic limits are satisfactorily clarified. the scutum and scutellum (Fig. 7). Genera assigned to the tribe in addition to Doiranio Key to species of Doirania include OUgosita, Megaphragma, Prestwi- (Traits pertain to females unless indicated) chia, Epoligosita, Prosoligosita, Chaetos- 1. Ovipositor elongate, V4-V3 longer than hind tib- trichella, Hayatia, Eteroligosita, and Pro- ia, extending slightly beyond cerci (Fig. 9). brachista. De Santis (1997) also assigned Male genitalia elongate, ca. '/, longer than hind his new genus Brachistagrapha to this tribe tibia, with apodemes curving laterally at base (Fig. 17). Forewings with a small but distinct but, known only from females, its place- fumate cloud near apex ofstigma. Known from ment requires confirmation. Papua New Guinea and Ambon, Indonesia . . Doirania is separated from all other oli- D. leefinansi gositine genera by the following combina- - Ovipositor shorter, its length ranging from dis- tion of characters: Foramen magnum placed tinctly less than to subequal to hind tibial length, not quite attaining level of cerci (Fig. near top of head (Fig. 1); antenna (Fig. 4) 8). Male genitalia shorter, length only 0.5-0.6 with a single club segment and a transverse that of hind tibia, with apodemes straight, not funicle; three or more metasomal terga with curving laterally at base (Fig. 16). Forewing a longitudinally striate posterior section (Fig. 15) at most slightly darkened at apex of stigma, without a distinct fumate cloud 2 (Figs. 13, 14); ovipositor relatively short, 2. Metasomal terga with longitudinally striate not extending beyond apex of metasoma; posterior section distinct, at least second and male genitalia simple (Figs. 16, 17), tubular, third visible terga with striate section ca. twice without complex apodemes basally. Certain the length of uniformly sclerotized anterior PROCEEDINGS OF THE ENTOMOLOGICAL SOCIETY OF WASHINGTON 354 Figs. 1-6. 1. Doirania elegans, posterior view of head. 2, Epoligosita sp. (same). 3, Doinmia elegans, rigiit maxillary palp (ventral). 4, D. elegans. antenna (lateral). 5, D. elegans, sensilla on dorsum of forewing disk anterior to retinaculum (see arrow in Fig. 15 for location). 6, D. leefniansi (same). — section (Fig. 13). Male club distinctly longer Description. Female: Body length than scape. New World D. elegans, new species 0.44-0.75 mm. Medium to dark brown in Meta.somal terga with longitudinally striate color except face, legs and antenna lighter posterior section relatively indistinct, sclero- tized striae poorly distinguished from adjacent brown; forewing only slightly fumate be- membrane, terga with striate section, at most, neath venation. Head: Antenna (Fig. 4) subequal in length to uniformly sclerotized an- with toruH at level of ventral margin of terior section (Fig. 14). Male club shorter than eyes; scape and pedicel together 1.2X com- scape. Palaearctic D. longiclavata bined length of funicle and club; club 1- segmented; mean length/width of antennal Doirania elegans Pinto, new species segments as follows: scape, 2.76; pedicel, (Figs. 1, 3-5, 7, 8, 11-13, 15, 16) 1.95; funicle, 0.67; club, 2.24; relative Two forms (A & B) of this species are length of antennal segments in same order: recognized (see Variation). The description 47/37/14/56; club 1.2X as long as scape, based on North American specimens of with terminal sensillum (= UPP trichodea is Form A. Unless indicated, quantitative data D of Olson and Andow 1993) setiform (see are based on five specimens from different Variation), 0.45 segment length (Fig. 11), locales; data represent means unless report- placed on a small apical truncate pedestal; MPP ed as a range. longest flagelliform setae (= trichodea — VOLUME NUMBER 106, 2 355 A) 0.65 club length. Maxillary palp narrow- In Form A the terminal club sensillum in ing asymmetrically to apex, with apical sen- females is setiform (Fig. 11) and is similar sillum longer than half the length of adja- in dimensions to the numerous flagelliform cent seta (Fig. 3). Mesosoma: Propodeum setae on the same segment; also the ovi- transverse (Fig. 7). slightly arcuate at mid- positor is relatively short (see above). In dle and slightly longer (<2X) than meta- Form B, the terminal sensillum is broader notum. Hind femur ca. 0.3 as wide as long; and, although tapering, it remains slightly tarsi relatively short, pro-, meso- and meta- truncate at the apex rather than acuminate tarsi ca. 0.80, 0.75 and 0.75 the length of (Fig. 12). Also the ovipositor is longer in their respective tibia; segment I slightly Form B [0.98 (0.87-1.14, n = 12) as long shorter than II and III on fore- and middle as hind tibia], and the discal forewing setae legs, all tarsomeres subequal on hind legs. are usually shorter. I am unable to distin- Forewing (Fig. 15) 2.5-3.OX as wide as guish the males of these variants. Although long, longest fringe setae 0.4—0.5 maximum the two forms are not geographically dis- wing width; sensilla anterior to retinaculum junct there is a degree of character overlap. on dorsal surface of disk relatively large, Additional material and study is required to digitiform, usually clavate (Fig. 5). Hind determine if this variation is taxonomically wing with 2 complete tracks of setae on significant. A disk, a partial third track present at apex in small series from Ecuador (Limonco- some specimens. Metasoma: Terga anterior cha, Napo Province) consisting only of fe- to VII clearly differentiated into an anterior, males is questionably conspecific to D. ele- uniformly sclerotized section and a poste- gans. In these specimens the propodeum is rior longitudinally striate section; striate more distinctly produced at the middle, and section elongate, twice as long as anterior the pedicel is subequal in length to the section on most terga (Fig. 13). Venter (Fig. scape. Ovipositor length and the form of the 8) with all visible sterna except hypogyn- terminal club sensillum are as in Form A. ium narrowly divided longitudinally; hy- Types.—Holotype 9. UNITED STATES. pogynium broadly emarginate; first visible Oklahoma: Red Oak (Latimer Co.); ix- sternum with a distinct posterior longitudi- 1993; flight intercept trap (FIT); K. Ste- nally striate section, others obsolescently phen. Paratypes, 2 (5, 1 9 with same data. striate posteriorly. Ovipositor 0.76 (0.67- Holotype and one male paratype deposited 0.89, n = 10) as long as hind tibia (see in Canadian National Collection, Ottawa Variation). (CNC); the two additional paratypes depos- Male: As in female except antennal club ited in the Entomology Department. Uni- with only 3 placoid sensilla (1 basal, 2 near versity of California. Riverside. Types are apex), and fewer flagelliform setae; club mounted in Canadian balsam on glass longer than scape (1.1-1.4 as long); only slides. Seven carded females from the same anterior 3 metasomal terga with an obvious series are not designated as types. The posterior striate section. Venter with a me- slide-mounted types belong to Form A. dial, posteriorly projecting lobe on antepen- Diagnosis. Doirania elegans is closest tultimate sternum (as in Fig. 10, see Re- to the Palaearctic species. D. longictavata. marks); lobe only slightly longer than wide. It is separated by the more distinct and lon- Genitalia (Fig. 16) gradually but distincdy ger striate section of the metasomal terga widened to apex, length 0.5-0.6 that of hind (see key to spp.). Also, in the male of D. tibia, with basal apodemes straight, not elegans the club is distinctly longer than the curved laterally. scape, not shorter as in D. longiclavata. — Variation. There appears to be two Sensilla anterior to the retinaculum on the & sympatric forms (A B) of this species. dorsal surface of the forewing apparently The description and types refer to Form A. provide an additional difference. In the new PROCEEDINGS OF THE ENTOMOLOGICAL SOCIETY OF WASHINGTON 356 Figs. 7-10. Doirania. 7, D. elegans. mesosoma (dorsal). 8, D. elegans, metasoma (ventral). 9, D. leefiminsi, metasoma (ventral). 10, D. leefmansi, apex of metasoma (ventral). species they are rather elongate, digitiform longiclavata resemble Form A of D. ele- and often clavate (Fig. 5); in D. longicla- gans. vata, as in D. leefmansi as well, they are Although very similar phenetically, it is shorter and typically acuminate apically not yet clear if D. elegans and D. longicla- (Fig. 6). Ovipositor length and shape of the vata are sister species. The only similarity apical antennal sensilla in females of D. which may be derived is the asymmetrically VOLUME NUMBER 106, 2 357 narrowed maxillary palp (Fig. 3). It occurs Highlands Hammock (Highlands Co.); ix- in both species but not in D—. leefmansi. 18-1987; sweep; 2 9; L. Masner (A/1). Geographic distribution. Eastern Unit- Georgia: Athens (Whitehall Forest); ix-14/ ed States, Arizona, southeastern Canada, 28-1987; flight intercept trap, hardwood with a single record of questionable con- forest (beaver swamp); 9; CNC Hym. 1 specifics from Ecuador. Team (A). Sapelo Island; vii-18/ix-l 1-1987, — Remarks. Hosts are unknown. Several ix-9/21-1987, x-15/xil6-1987; Malaise of the records (see below) suggest that D. trap; live oak forest; 14 9, 1 S: CNC Hym. elegans occurs in relatively mesic habitats. Team (A/4). Tifton, 13 km NW; ix-25/x-17- Males of Doirania and of related senera 1985; pan trap; 2 9; M. Keller (A/1). Illi- are characterized by at least one medial pro- nois: Centralia (along roadside: Hwy 51 & longation on the sternal region of the me- Bethel Rd.); yellow pan trap "among weeds tasoma (Pinto and Viggiani, in preparation). nr. soybeans"; ix-12/17-1995; 2 9; S. The few males available of D. elegans and Triapitsyn (A). Centralia, 3 mi N; ix-12/17- D. longiclavota are mounted on slides and 1995; yellow pan trap "in grass nr. pond"; do not allow adequate description of this 1 9 ; S. Triapitsyn. Centralia, 2 mi S (of structure. However, it appears to be similar downtown); ix-13/17- 1995; yellow pan trap to that occurring in D.—leefmansi (Fig. 10). "on edge of forest"; 1 9; S. Triapitsyn. Material examined. 136 9, 8 (5. Iden- Centralia, 8 mi E; ix-7-1993; sweeping tification of 'form' (A or B) is possible for "open field"; 2 9 ; J. Pinto. Litchfield; x-3- slide-mounted females only. Consequently 1983; sweep; 9,1 S\ J./D. Huber (A). 1 & an indication of 'A' or/and 'B" does not fol- Marion Co. (Myers Rd. nr. hwys. 57 low those records based only on males or 161); ix-12/17-1995; yellow pan trap "in carded females. In cases where both slide- grass in swampy area"; 9, d; S. Triap- 1 1 mounted and carded females are available, itsyn. Kansas: Manhattan, 2 mi S; ix-6- the number of individuals that identification 1983; (sex undetermined); J./D. Huber. 1 W of 'form' is based on is indicated (e.g.. A/ Wauconda Lake (2 mi Glen Elder, 2, signifies that two of the females in the Mitchell Co.); viii-28-1985; sweep; 1 9; J. series were slide-mounted and identifiable Pinto. Maryland: Port Republic; viii/ix- to form). 1986; flight intercept trap; 9 9, 6: M. 1 CANADA. Ontario: Ottawa (Innes Sharkey/Munroe (B/1). Prince Frederick, 7 Point); viii-20/27-1985; 1 9 ; L. Dumochel/ km S; v-7/vii-7-1987; 1 9; CNC Hym. J. Denis (B). Powell's Lake (105 km NE Team. Missouri: Columbia (Hinkston Lake Superior); viii-16-1980; 1 9; M. Creek); ix-8-1987; sweep; 1 9; J. Pinto. Kaulbars. Shirley's Bay; viii-27/ix-10-1985; Williamsville (Wayne Co.); vii-16/viii-8- 9; M. Sanborne/H. Goulet. UNITED 1988, viii-1987, viii-8/31-1988, ix-1/20- 1 STATES. Arizona: Brawley Wash (Pima 1988, ix- 10/26-1987, ix-20/x-20-1988. x- Co.); viii-3-1982; 1 9 ; G. Gibson (A). No- 21/xi-l 1-1987; Malaise trap; 38 9, 2 S\ J. gales (N edge of town); ix-27-1985; sweep- Becker (A/3. B/5). Nebraska: Odessa, 6.8 ing; 1 9 ; J. Pinto (A). Florida: Archbold mi E; viii-29-1983; 2 9; J. Pinto (A). Biological Research Station; x-27/xi-30- Oklahoma: Red Oak (Latimer Co.); 9 9,2 1988; Malaise trap; 2 9 D. Wahl (A/1). 6; (see Types). North Carolina: Whiteside ; Bradenton; x-19/26- 1985; sweep; 9; C. Mtn. (Jackson Co.); ix- 13-1987; sweep; 3 1 Yoshimoto. Everglades National Park 9; L. Masner (B/1). South Carolina: Fran- & (Long Pine Key); vi-6/viii-26, viii/xi- cis Beidler Forest (nr. Harleyville); ix-22- 986; Malaise/flight intercept trap; 6 9 S. 1987; sweep; 9 L. Masner (A). Francis ; 1 ; & km NE J. Peck (A). Gainesville; iv-17/23- 1988; Beidler Forest (10 Harleyville); v- 1 (sex undetermined); D. Wahl. GaWinesville; 26/vi-l 1-1987; flight intercept trap; "bald iv-8/14-1987. xii- 1/7- 1986; 2 9; Mason. cypress swamp"; 1 9. Pendleton (Tangle- PROCEEDINGS OF THE ENTOMOLOGICAL SOCIETY OF WASHINGTON 358 — wood Springs; 34°38.7'S. 82°47.1'W; 225 Material examined. FRANCE. Dept. m); vii-30/viii-20-1987, ix-1/9-1987, ix-15/ Gironde: St. Colombe (nr. Castillon-la-Ba- 30-1987, x-16/xi-3-1987; Malaise trap; 6 taille), 44°54'N, 00°02'W; viii-17-2000; 9; J. Morse (A/1). Pendleton (225 m); vii- suction trap; 1 9 ; M. van Helden. JAPAN. 15/22-1987. vii-29/viii-5-1987; Malaise Kyushu: Fukuoka (Mt. Tachibana); viii-26/ trap; 2 9; CNC Hym. Team (A/1). South 31-1979; yellow pan traps, "primarily ev- Dakota: Pickstown (Charles Mix Co.); viii- ergreen forest"; 4 9; K. Yamagishi. Hon- 26-1985; "sweeping riparian"; 4 ?; J. Pin- shu: Iwate (Mt. Hayachine); 400 m; viii-2/ NW to (A/1, B/1). Texas: Ben Bolt, 8 mi 8-1989; Malaise trap; M. Sharkey. [Several (La Copita Res. Stn.); ix-28/30-1990; Mal- additional Japanese records cited by Yosh- aise trap; 1 9 ; R. Wharton/J. Woolley. Cly- iro 1980]. RUSSIA. Primorskiy Krai: Ta- mer Meadow (Hunt Co.); vii-9-1991; jvaza (30 mi NE Vladivostok); flight inter- sweep; 1 9; J. Woolley (A). College Sta- cept trap "coastal forest"; viii-5-1992; 5 9, tion; viii-26-1987; 1 9; J. Woolley/G. Zol- 1 (5; B. Gill. Krasnodarskiy Krai: Krasno- nerowich (B). College Station (Lick Creek dar, nr. (All Russian Research Institute of Park); vii-30-1987; sweep; 1 9; J. Woolley. Biological Plant Protection); viii-30/31- College Station (Lick Creek Park); x-16/xi- 2001; yello—w pan trap; 1 9 ; V. Kustjukov. 17-1987; sweep; 1 9 ; J. Woolley/J. Heraty. Remarks. Hosts are unknown. As with Hallsville, 2 mi W; Wiv-27-1984; sweep D. elegans, D. longiclavata apparently fre- "roadside forbs"; 1 9; Ewart (B). Hear- quents mesic habitats. Yashiro (1980) states ne, 8 mi. E.; x-22/27/1990; Malaise trap; 1 that the species has been collected in "pad- 9.1 d; J. Woolley, et al. Park Hill Prairie dy fields and grassplots." (Collin Co.); vii-9-1991; 2 9 ; J. WoolNleWy km (B/1). Virginia: Blacksburg, 8 Doirania leefinansi Waterston (1000 m); vi-9/19-1987, vi- 19/30- 1987, vii- (Figs. 6, 9, 10, 17) 13/19-1987; Malaise trap; 6 9; CNC Hym. Team (A/2). Doirania leefinansi Waterston 1928: 286; Yashiro 1980: 133; Doutt and Viggiani Doirania longiclavata Yashiro 1968: 499; Viggiani 1971: 209; Caudwell (Fig. 14) 2000: 218. — Doirania longiclavata Yashiro 1980: 131. Diagnosis. Female. Body light brown — Diagnosis. Similar to D. elegans except in color. Antenna with scape subequal in for the more poorly defined striate section length to club. Maxillary palp regular at of the metasomal terga (cf. Figs. 13, 14), apex, not narrowing asymmetrically. Fore- the smaller club/scape ratio in males, and wing with a small fumate cloud directly be- the differently shaped sensilla at the base of hind stigma; sensilla anterior to retinaculum the forewi—ng (cf. Figs. 5, 6). on dorsal surface of disk small, acuminate Types. Holotype 9, from JAPAN, (Fig. 6). Ovipositor elongate, distinctly lon- "Hatadera, Matsuyama City, Ehime Pref., ger than hind tibia, extending beyond cerci Shikoku"; x-19-1977; N. Yashiro; "on (Fig. 9). Male. Antenna with scape also turfs"; presumably in the Entomological subequal to club. Genitalia elongate, ca. '/^ Laboratory, University of Osaka Prefecture longer than hind tibia, with basal apodemes (inquiries regarding the holotype were un- directly laterally (Fig. 17). answered). Types.—Holotype 9, "Ambon (D.E.I.)" — Geographic distribution. Previously re- (currently Indonesia) from "eggs of Sexava corded only from Japan, but probably wide- coriaceaT iv-30-1925, S. Leefmans coll.; spread in Palaearctic. Currently known stated to be in The Natural History Muse- from Japan, eastern Russia, and France. um, London (Waterston 1928) but not lo- VOLUME NUMBER 106. 2 359 Figs. 1 1-17. Doirania. \l. D. elegans. antenna (Form A) (arrow at apical sensillum). 12. D. clegans. antenna (same. Form B). 13. D. elegans. metasoma (dorsal). 14. D. longiclavata, (same). 15, D. elegans. forewing (arrow at location of disk sensillae: see Figs. 5. 6). 16. D. elegans. male genitalia (venter, arrow at basal apodemes). 17, D. leefmansi (same). — PROCEEDINGS OF THE ENTOMOLOGICAL SOCIETY OF WASHINGTON 360 cated (4 9 paratypes with same data as ho- Doutt, R. L. and G. Viggiani. 1968. The classification of the Trichogrammatidae (Hymenoptera: Chalci- lotype examined). — doidea). Proceedings of the California Academy Geographic distribution. Known from of Sciences (4th series) 35: 477-586. Indonesia (Ambon) and Papua New Guin- Gibson, G. A. P. 1989. Phylogeny and classification of ea. — Eupelmidae, with a revision of the world genera Material examined. INDONESIA: Am- of Calosotinae and Metapelmatinae (Hymenop- bon (see Types). PAPUA NEW GUINEA tera: Chalcidoidea). Memoirs of the Entomologi- Dami, West New Britain; ix-29-1991; T. M cal Society of Canada. No. 149, 121 pp. 1997. Morphology and terminology. Chap. 2, Solulu; 11 9, 1 6. New Hanover [Isl.] pp.. 16-44. //; Gibson, G. A. P, J. T Huber, and 1932; 'ex. eggs of locustid'; J. L. Froggatt; J. B. Woolley, eds. Annotated Keys to the Genera 9. Culture material reared in Papua New of Nearctic Chalcidoidea (Hymenoptera). NRC 1 Guinea, of unknown origin, 10 9, 6. Research Press, Ottawa, Canada, 794 pp. 1 Hayat, M. and B. R. Subba Rao. 1985. Family Tricho- Remarks. Doirania leefmcmsi is known grammatidae, pp. 239-245, 304-308. In Subba to attack eggs of species of Tettigoniidae Rao et al., eds. The Chalcidoidea (Insecta: Hy- {Segestes spp.), pests of oil palm, in Papua menoptera) of India and the adjacent countries. New Guinea. Although their role in affect- Part I. Reviews of families and keys to families and genera. Oriental Insects 19: 163-310. ing pest populations is questionable, these Olson, D. M. and D. A. Andow. 1993. Antennal sen- wasps continue to be cultured and released silla of female Trichograninia niibilale (Ertle and into oil palm growing areas (Caudwell Davis) (Hymenoptera: Trichogrammatidae) and 2000). comparisons with other parasitic Hymenoptera. International Journal of Insect Morphology and Acknowledgments Embryology 22: 507-520. Pinto, J. D. 1997. Trichogrammatidae. Chap. 22, pp. Gary Platner was responsible for speci- 726-752. //; Gibson, G. A. P, J. T Huber, and J. men and plate preparation, and assisted B. Woolley, eds. Annotated Keys to the Genera of with photographs. This study was supported Nearctic Chalcidoidea (Hymenoptera). NRC Re- by grants from the USDA (NRI) and NSF search Press, Ottawa, Canada, 794 pp. (PEET). Material studied came from nu- . 1999 (1998). The systematics of the North American species of Trichogramma (Hymenop- merous sources, the greatest number from tera: Trichogrammatidae). Memoirs of the Ento- J. Huber of the Canadian National Collec- mological Society of Washington, No. 22, 287 pp. A&M tion and J. Woolley, of Texas Uni- Viggiani, G. 1971. Ricerche sugli Hymenoptera Chal- cidoidea XXVIII. Studio morfologico comparati- versity. vo delTarmatura genitale esterna maschile dei Tri- Literature Cited chogrammatidae. Bollettino del Laboratorio di Entomologia Agraria 'Filippo Silvestri' di Portici Caudwell, R. W. 2000. A sustainable IPM system for 29: 181-222. oil palm in Papua New Guinea. The British Crop Waterston, J. 1928. On a trichogrammid {Doirania Protection Council Conference, Pests & Diseases leefmansi, gen. et sp. n.) reared from eggs ofSex- I: 215-220. ava (Orth.) in the Dutch East Indies. The Annals De Santis, L. 1997. Afeli'nidos y Tricogramatidos de and Magazine of Natural History (10)2: 386-388. la—coleccion del Dr. Alejandro A. Ogloblin (Insec- Yashiro, N. 1980. A new species ofthe genus Doirania ta Hymenoptera). II Segunda Comunicacion. from Japan (Hymenoptera: Trichogrammatidae). Academia Nacional de Agronomia y Veterinaria Transactions of the Shikoku Entomological Soci- 51: 8-17. ety 15: 131-134.