Anzeiger fiJr Sch idlingskunde Journal of Pest Science 72. J a h r g a n g 9 H e f t 3 - J u n i 1 9 9 9
Anz. Sch~idlingskunde/]. Pest Science 72, 57-61 (1999) 9 1999, Blackwett Wissenschafts-Verlag, Berlin ISSN 1436-5693
Forest Research Institute, Sofia, Bulgaria and Biological Fac,:lry of the University =St. KL Ohridski', Sofia. Bulgaria
New Ichneumonidae (Hymenoptera) parasitoids of forest insect pests in Bulgaria By G. GEORGIEV and J. KOL.~ROV Abstract During the period 1989-1998 investigations were carried out on the parasitoids of some forest insect pests in Bulgaria. Twenty-one ichneumonid species are reported for the first time in Bulgaria as parasitoids of different coleopteran, lepidopteran, and hymeuopteran hosts. From these, 6 parasitoids are new records for the parasitoid complexes of the hosts: Exochus deeoratus Holmgr. on Eudemis profundana (Den. & Schiff.) and Gelechia tut~ella (Den. & Schiff.); Lissonota culiciformis Gray. - on Paranthrevze tabaniformis (Rott.); Lissonota unicineta Holmgr. - on G. turpella; Xorides graciEcornis (Gray.) - on Xylotrechus sp.; and Eriborus terebrator Aubert on Clostera anastomosis (L.). Most parasitoids developed as primary parasitoids in the hosts, hoplectis alternans (Gray.) is a primary parasitoid of Nycteola asiatica (KruL) and a hyperparasitoid of E. terebrator. Acropimpla pictipes (Gray.) is secondary parasitoid on Anacampsis populella (CL). With the exception of two species of Olesicampe genus, which destroyed over 50 % of Stauronenuztus compressicornis (E) and Pristophora conjugata (Dahlm.) larvae, and E. terebrator which kil~ led 15.4 % of C. anastomosis population, the rest of the parasitoids occurred in" low densities, and did not play an important role in reducing the number of their hosts. 1 Introduction
The forest trees and shrubs are related trophically with many phymphagous insects. Most of these herbivore populations occur in low densities and usually do not act as pests. There are also species, which periodically increase in density and cause serious damage to the forest stands. Their number is limited by different natural abiotic and biotic - factors. Parasitoids occupy a special position in the biotic limiting complex since they regulate the population densities of the pests at a relatively low number, thus being one of the main factors for the sustainability of the forest ecosystems. The Ichneumonidae family is the most numerous parasitic insect group, including over 4000 valid species in the Western Palaearctic (TowNES, 1969). Many faunistic investigations have been carried out in Bulgaria on this family (GREGOR, 1933; HEiNRICH, 1936; CANKOV, 1968; KOLAI~OV, 1997; etc.). The hosts of some ichneumonid species in the forest ecosystems and in the agricultural plantations have been investigated as well (ZAPIqANOV, 1985, 1989; GANCHEV, t990; etc.). However, it should be noted that the trophical relationships of the ichneumonids with the phytophagous insects in the forests
of the country as a whole have not yet been well stu-died. This paper presents new parasitoid-host relationships in Bulgaria between some species of Ichneumonidae and forest insect pests. 2 Materials and methods The investigations discussed here were conducted during 1989-1998 and were part of series of studies on the parasitoids of forest insect pests in Bulgaria. Phytophagous hosts were collected in larval and pupal stage on different forest tree and bush species and parasitoids were reared in the laboratory. After collection, phytophagous larvae and pupae were transported to the Forest Research Institute laboratory, in Sofia where they were separated according to species and reared at room temperature (18-22 ~ The iarvae of the defoliators were fed with fresh leaves of the host plants in glass dishes as the specimens pupated. The pupae were placed individually in test tubes and closed with cotton stoppers. The larvae of xylophagous hosts were reared within cuttings of shoots, branches and stems of approximate length 25-30 cm. The sections of the cuttings were covered with paraffin, and each cutting was reared individually in a glass cylinder or in an entomological box. The samples were observed daily for emergence of parasitoids and hosts. At the end of ~he observation period, a detailed study of either individual host was performed in order to determine the cause of mortality and to reveat the characteristics of the parasite-host relationships. Emerged insects were killed with etylacetate, identified and deposited in the author's collections. 3 Results
As a result of this investigation 23 parasite-host relationships between 21 ichneumonid species and 17 forest insect pests were recorded for the first time in Bulgaria (table 1). The new parasitoids were found in various localities of the country, (fig. 1). The parasitoids belong to 15 genera of 7 subfamilies of Ichneumonidae family as follows: Pimplinae: Acropimpla piccipes (Gray.), Itoplectis akernans (Gray.), [toplectis rnaculator (Fab.), and Scambus vesicarius (Ratz0; Xoridinae: Xorides gracilicornis (Gray.); Cryptinae: Agrothereutes adustus (Gray.), and Pleolophus basizonus Gray.; Banchinae: Apophua bipunctoria (Thunb.), Lissonora caliciformis Gray., and Lissonota unicinera Hotm.; Ctenopelmatinae: Rhinotorus sp.; Campopleginae: Rhimphoctona (R.) grandis B. de Fons., Nerneritis sp., Tra-
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G. GEORGIEVand J. KOLAROV,New parasitoids of forest insects in Bulgaria
58
noserna rostralis (Brischke), Diadegrna aposmta (Gray.), Olesicampe sp. 1, Olesicampe sp. 2, Lathrostizus tugens (Gray.), Eriborus terebrator Aubert, and Eriborus sp.; Metopiinae: Exochus decoratus Holm. Two species - E. terebrazor and R. grandis are new reports for the fauna of Bulgaria (table 1). The parasitoids were reared from coleopteran, lepidopteran, and hymenopteran hosts, which belong to 8 families (table 1). Six ichneumonids are new records for the parasitoid complexes of the hosts. E. decoratus was found for the first time on Eudernis profundana (Den. & Schiff.) and Gelechia turpella (Den. & Schiff.), L. culMformis - on Paranthrene tabaniformis (Rott.), L. unicincta - on G. turpella, X. gracilicornis - on Xylotrechus sp., and E. terebrator- on Clos~era anastomosis (L.) (table 1). All of the parasitoids found on the hosts were solitary. Most of them developed as primary paraskoids. I. alternans was observed as a primary parasitoid of Nyczeola asiatica (Krul.) and as a hyperparasitoid of E. terebrator (primary parasitoid of C. anastomosis). A. pictipes was secondary parasitoid, it was reared from one unidentified specimen of Ichncumonidae family on Anacampsis pop,della (C1.). Two species of Olesicarnpe caused high mortality levels of the hosts. In Petrich Olesicampe sp. 1 destroyed 63.2 % of Stauronematus compressicornis (E) larvae (table 1). In Sofia 66.7 % of the larvae of Pristiphora conjugata (Dahtm.) were parasitized -52.4 % by Olesieampe sp. 2, and 14.3 % by Rhinotorus sp. E. terebrator was responsible for killing of 15.4 % of the C. anastomosis population in Kokaliane. However, L ahernans hyperparasitised a significant portion (25.0 %) of E. terebrator larvae, thus limiting the potential impact of the primary parasitoid. The rest of the parasitoids were in relatively low densities, and did not play an important role in reducing the number of their hosts.
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4 Discussion
E. terebrator is distributed in Mediterranean and Central Europe (HoRSTMANN, 1987). It is recorded for the first time on C. anastomosis in this study. No other hosts of E. terebrator have been found in the entomological literature. R. grandis belongs to a small holarctic genus including about 10 species in Europe (MEDvEDIEV, 1981). The representatives of this genus are known as parasitoids of Cerambycidae and Raphidiidae (To~'NES, 1970). R. grandis is a very rare species. ]t was already recorded in other countries as a parasite of Saperda carcbarias (L.) (OZOLS, 1928; STROJNu 1954). However, STROJNY(t954) reported R. grandis under the synonym Rhimphoctona fulvipes Holmgr. A. pictipes has been previously reported in Bulgaria (KOLAROV, 1984b) and observed as a parasitoid of Tortficidae sp. (GANTCHEV, 1977). S. vesicarius has been reared in Bulgaria only from larvae o f P tabaniformis (KoLAa.OV & GEO~.GIEV, 1997) but in other countries it is known as a parasitoid of many hymenopteran and lepidopteran species (FH-rON et aL, 1988). A. adustus has been previously reported in Bulgaria (HEINRICH, 1936; CANKOV, 1968) and found as a parasitoid of Diprion pini (L.) (BoCHEV & GEORGIEV, 1996; GEORGIEV & BOCHEV, 1996). However, the species is well known as a parasitoid of Neodiprion serrifer (Geofft.) (PSCHORN-\YgALCHER,1982). P. basizonus is established in Bulgaria as a parasitoid of .~: sertifer (ZANKOV & DASK,XLOVA, 1971) and has been previously reported in the c o u n t ~ by KOLAROV(t990a). It parasitizes Diprzon similis (Htg.), D. pini, Gilpinia frutetorum (Fabr.), G. polytorna (Htg.), G. pallida (Klug), N. sertifer, and Microdiprwn pallipes (Fall.) (Hymenoptera: Diprionidae) (PscHORN-WALCHER, 1982).
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G. GEORGIgV and J. KOLAROV,New paraskoids of forest insects in Bul~aria
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G. GEORGIEVand J. KoI.,~ROV,New parasitoids of forest insects in Bulgaria
L alternans, I. rnaculator, A. bipunctoria and D. aposrata were recorded from a wide range of hosts (MEDvEDIEW 1981). In Bulgaria, L alcernans was found in many tepidopteran species - Yponomeuta matlinellus Zeti. (Yponomeutidae), Ostrinia nubitalis (Hb.) (Pyralidae), Anarsia lineatella Zell. (Gelechiidae), Acleris bergmanniana (L.), Cnephasia pasiuana (Hb.), Cydia molesta (Busck), Lobesia botrana (Den. & Schiff.), Torwix viridana L. (Tortricidae) and Euprocris ch~ysorrhoea (L.) (Lymantriidae) (KoLAROV, 1997). I. maculator was recorded in Bulgaria as a parasitoid of Pieris brassicae (L.) (Lep.: Pieridae), Lymantria dispar (L.) (Lymantriidae), Archips rosana (L.) and T. viridana (Tortricidae) (KOL.~ROV, 1997). A. bipunctoria is known in Bulgaria as a parasitoid of A. bergmanniana CI'scHO~ADj~EV, 1933), Agonopterix ocellana (E) (Lep., Depressariidae), Pandemis cerasana (Hb.) (= P ribeana Hb.) (Lep., Tortricidae) (NIKoI_ovA, 1962), T. viridana, A. xylosteana (GA>rrCHEV, 1977) and Pandemis dumetana Cir.) (Lep., Tortricidae) (ZAPRjANOV, 1985). D. apostata has been previously reported in Bulgaria by KOLAROV(I 990a) and found as a parasitoid of Cnaemidophorus rhododactyla (Den. & Schiff.) (Lep, Pterophoridae) (NIKOLOVA, 1954), Cydia funebrana (Treitschke) (Lep., Tortricidae) (ToSHKOVA-TsVETKOVA, 1960), A. xylosteana (KoLEV, 1971) and Tortricidae sp. (GANTCHEV, 1977). L. lugens is reported (with synonymous name Angieia vestigialis Ratz.) in Bulgaria as a parasitoid of L. botrana (HARIZANOV, 1979). L lugens is distributed in Central Europe and it is connected mostly with Nematus oligospilus F6rster (Hym., Tenthredinidae) (MEDVEDIEV,1981). This parasitoid is connected also with Pontania capreae (Lep.) and other Pontania species (HoRSTMANN, 1971). In our investigations L. lugens has been reared from Pontan/a sp. (viminalis-group). In Europe the viminalis-group from this genus includes many monophages on different willows (ZI.Novj~v, 1995). The rest of the parasitoids were found in Bulgaria only in faunistic studies. L. culiciforrnis was reported by KOLAROV(1984a, 1998); L. unicincta bv GREGOR (1933); X. graciticornis by KOLAt~OV(1997); T.. rostralis by KOLAROY (1990a, b); and E. decoratus by GEP,MA_,','OV(1980) and KOLAROV (1990a). In other countries of Europe L. unicincta is known as a parasitoid of Agonopterix thapsiella (Z.) (Lep., Oecophoridae) (AUBERT, 1978). This species is reared also from a unidentified host in strobides of Picea abies (L.) Karst, (Plsma & PETCU, 1972). L. culiciformis parasitizes some xylophagous insects, Tortrix sp. and S. ocellana (AuBERT, 1978). X. gracilicornis is distributed in Central and South Europe (MI~DVEI31EV, 1981). Until now, no hosts of X. gracilicornis and T. rostralis have been recorded. E. decoratus is distributed in all Holarctis (MEDVEDIEV, 1981), but there is no data about its hosts in the entomological literature. In conclusion, most of the parasitoids occurred in low densities and they were not important as limiting factors of the forest insect pests. However, new records increase the species strength of the Bulgarian fauna and enrich the host ranges of some ichneumonid species.
Acknowledgements We are grateful to Dr. N. VELCHEVA,Plant Protection Institute - Kostinbrod, and S. BESHKOV,National Museum of Natural History - Sofia, for identifying some lepidopteran hosts of
the parasitoids. We also thank Dr. FERNANDOE. VEGAand Dr. FRANCK HERARD, European Biological Control Laborato,'?, Montpelier - France (Agricultural Research Service, United States Department of Agricukure), for critical reading and revising the English version of the manuscript.
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G. Gt.o~talEv and J. KOLAROV,New parasitoids o{ forest insects in Bulgaria
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Authors' addresses: Dr. GEORGI GEORC.I~-;v,Forest Research Institute, 132 Kliment Ohridski Blvd., 1756 Sofia, Bulgaria; Dr. J^NKO KOLagOV, Biological Faculty, University of Sofia "St. KI. Ohridski", 8 Dragan Zankov Bird., 1421 Sofia, Bulgaria
Heinrich Hofmeister
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