Biodiversity Data Journal :
Taxonomy & Inventories
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Corresponding author: Ivaylo Todorov (i.toddorov@abv.bg)
Academic editor: Simon van Noort
Received: 15 Oct 2024 | Accepted: 18 Nov 2024 | Published: 03 Dec 2024
© 2024 Ivaylo Todorov, Mircea-Dan Mitroiu, Aneliya Bobeva, Peter Boyadzhiev
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Todorov I, Mitroiu M-D, Bobeva A, Boyadzhiev P (2024) Description of Mesopolobus askewi sp. nov. (Hymenoptera, Pteromalidae), with notes on the fauna of Asaphesinae and Pteromalidae (Hymenoptera, Chalcidoidea) collected from foliage of Picea abies (L.) H. Karst. in Bulgaria. Biodiversity Data Journal 12: e139403. https://doi.org/10.3897/BDJ.12.e139403
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Mesopolobus Westwood, 1833 consists of about 135 valid species worldwide. After the fundamental monograph of Graham (1969), 12 species have been described from continental Europe and three species have been described from the Canary Islands and Malta. Amongst them, one species, Mesopolobus blascoi Askew, 1994, has been synonymised under Mesopolobus maculipennis (Mercet, 1923). Only eight species have been reported from Bulgaria to date.
Here we describe a new species, Mesopolobus askewi sp. nov. and present new data on the Bulgarian chalcidoid fauna obtained by sampling in foliage of the Norway spruce, P. abies. Mesopolobus askewi sp. nov. can be distinguished from the most morphologically similar species, M. longicollis Graham, by the following characters: clypeus with deeper emargination, fore wings with basal vein having complete row of setae, head blue to bluish-green, mesosoma bluish-green to green with coppery reflections, legs after coxae mostly fulvous, only distal one-fifth of meso- and metatibiae yellowish, protarsi with fifth segment yellowish, only tarsal claws fuscous, venation pale testaceous. Furthermore, we identified nine valid species of the family Pteromalidae belonging to four genera – Mesopolobus (three spp.), Pachyneuron (one sp.), Stenomalina (one sp.) and Trichomalus (four spp.) and one species of subfamily Asaphesinae (Chalcidoidea, incertae sedis), all represented in our samples by many specimens and none having previously been reported as associated with foliage of the Norway spruce. Three of the species are new records for the Bulgarian fauna.
Chalcidoidea, new species, new records, Bulgaria, mountain fauna, Norway spruce
Norway spruce, Picea abies (L.) H. Karst. (Pinaceae), is a Palearctic coniferous tree species distributed between the Alps in France and the foothills of the Urals. Its typical forests grow from 69°47’N latitude in Norway in the north to 41°45’N in Macedonia and Greece in the south, mostly in mountainous areas in central and south-eastern Europe, but also at lower altitudes in the Scandinavian Peninsula (
Having high economic and ecosystem value in forestry, P. abies has been in the focus of many studies and the insect fauna associated with spruce in Europe has been reported by many authors in the past. However, these investigations have dealt mostly with conophagous and seed species, as well as on saproxylic and xylophagous beetles and their natural enemies (
Pteromalidae are known to form a considerable part of the hymenopterous parasitoid complex of spruce pests. To date 23 species (
Mesopolobus Westwood, 1833 is one of the largest genera amongst all Pteromalidae and consists of about 135 valid species worldwide (
In the present paper, we describe a new distinctive species of genus Mesopolobus, namely Mesopolobus askewi and contribute to the knowledge of the pteromalid fauna associated with P. abies from Bulgaria with 10 new parasitoid-plant associations. The new species is discussed and compared to the most similar ones described in Mesopolobus after Graham’s revision (Graham 1969). Brief data about the known biology and distribution of the rest of the species are also presented.
All samples were collected by sweep netting from the lowest branches of the trees in forest stands of P. abies during July and August in the years 2019, 2020 and 2021. Selected localities were situated between 1014 and 2155 m above sea level in the Western Rodope Mountains and Stara Planina Mountains (= Balkan Mountains), Bulgaria. Gathered chalcidoids were caught individually by aspirator and fixed in 96% ethanol. The rest of the non-target insects in the net bag were released alive back in the field. The materials were dehydrated using absolute ethanol (Merck KGaA, CAS-No: 64-17-5, Germany) in the laboratory, treated with hexamethyldisilazane (Sigma-Aldrich®, USA, 99.9%) for two soaks of 1/2 hour each, air dried and mounted on card points for further observation. The specimens were studied under a Carl Zeiss Discovery.V8 stereomicroscope at 25–80× and photographed using a digital camera Canon EOS 200D attached to the intermediate photo tube by a T2-T2 DSLR 1.6 adapter. Stacking process was generated through Helicon Focus (v.7.5.8 Pro). Specimens used for scanning electron microscopy were mounted on brass stubs and coated with gold. SEM-micrographs were taken with a Lyra I XMU (Tescan) scanning electron microscope (with Quantax 200 Bruker detector) at 10 kV.
Genus and species identification followed the keys in
Total DNA was isolated from an individual insect using the DNeasy Blood & Tissue Kit following the manufacturer’s instructions. The extracted genomic DNA served as a template for amplifying two mitochondrial markers: Cytochrome c oxidase subunit I (COI) and Cytochrome b (CYTB). The primers used for polymerase chain reactions (PCR) were as follows: for COI – forward pF2 5’-ACCIGTDATRATRGGDGGITTYGGDAA-3’ and reverse 2413d 5’-GCTADYCAICTAAAAATYTTRATWCCDGT-3’ (
Five specimens of Mesopolobus longicollis Graham, 1969 - 3 females and 2 males, were provided for us by Dr. Richard Askew for comparison and are currently deposited in the entomological collection of the Institute of Biodiversity and Ecosystem Research. They are all labelled as follows: “England: Ainsdale, Lancashire; collected in 1977; leg Sulaiman Hanapi; em. V. 1978 from gall of Iteomyia major”.
Type specimens of Mesopolobus askewi sp. nov. and most of the specimens belonging to other species obtained in this study are deposited in the entomological collection of the Institute of Biodiversity and Ecosystem Research (Bulgarian Academy of Sciences, Sofia, Bulgaria). Ten specimens of M. askewi sp. nov. are deposited in the personal collection of R. R. Askew. Less numerous materials are deposited in MICO (Mitroiu Collection) in the Faculty of Biology, Alexandru Ioan Cuza University (Iasi, Romania).
Length: 1.7–2.1 mm.
Colouration (Fig.
Mesopolobus askewi sp. nov. Stereomicroscopic images:
Tegument. Head with upper face and vertex reticulate; lower face and genae reticulate to strigulate-reticulate; clypeus striate, striation not extending beyond sclerite margins; supraclypeal area reticulate; antennal scape and pedicel imbricate; Mesosoma: Pronotal collar and mesonotum reticulate, metanotum with lateral panels and dorsellum smooth and shiny; propodeum with median area between plicae weakly sculptured, shiny, median carina complete; propodeal plicae complete, sharp anteriorly and posteriorly, more rounded in the anterior third (Fig.
Head. 1.11-1.16x breadth of mesosoma, in dorsal view 1.94-2.0x as broad as long, temples 0.24-0.27x the length of eye (Fig.
Mesosoma. 1.52-1.58x as long as broad; pronotal collar long medially, about 1/6 to 1/5 (0.17 to 0.2x) length of mesoscutum (Figs
Fore wing. Marginal vein 1.10-1.23x as long as postmarginal vein and 1.60-1.75x as long as stigmal vein (Fig.
Gaster. 1.3-1.7x longer than wide, usually 0.72-0.92x shorter than, sometimes as long as head plus mesosoma; tip of hypopygium situated usually about at middle, rarely slightly before or slightly beyond the middle of gaster length; ovipositor sheaths well visible in ventral view, but hardly or not projecting beyond the last tergite.
Male. Unknown.
Mesopolobus askewi sp. nov. belongs to the group of species that have three anelli, long pronotal collar, which is one-sixth to one-fifth the length of mesoscutum and gaster usually slightly shorter than head plus mesosoma. It runs to couplet 36 in Graham’s key (
Updated key to females of M. askewi sp. nov. and M. longicollis (characters in Bold are interpolated in the couplets designed by
36 (34) |
Pronotal collar (Text-fig. 532) long, medially one-seventh to one-fifth as long as the mesoscutum, coarsely reticulate. Squat species with gaster usually slightly shorter than, rarely as long as, the combined length of head plus thorax, at least slightly less than twice as long as broad. Thorax golden green or bluish-green, head golden green to blue |
37 |
- |
Either the pronotal collar, medially, is at most one-eighth as long as the mesoscutum; or the gaster is about as long as head plus thorax and at least twice as long as broad and the head and thorax are bronze-green to bronze |
38 |
37 (36) |
Anterior margin of clypeus shallowly emarginated (Fig. |
M. longicollis |
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Anterior margin of clypeus moderately emarginated (Fig. |
M. askewi sp. nov. |
38 (36) |
= 37 (36) in the key of |
The first author is pleased to name this species after Dr. Richard Robinson Askew, one of the most prominent experts in the field of entomology, especially in the studies on Chalcidoidea. His works have been an inspiration for me since the beginning of my interest in the family Pteromalidae. In our correspondence Dr. Askew has always demonstrated his responsiveness and natural modesty and that have impressed me many times.
Unknown.
Probably native to Europe or at most to Western Palearctic and later introduced to North America. Records from Afrotropical and Neotropical Regions, as well as those from Greenland, have most likely been based on misidentifications (
Europe and north-western Turkey. New record for the Bulgarian fauna.
Western Palearctic and Nearctic.
Western Palearctic and Nearctic Regions. Probably with Holarctic range, but still not reported from North Africa and north-eastern Asia.
Following their original descriptions, females of most species in the genus Mesopolobus described after Graham’s monograph, can be easily recognised and distinguished from the pair longicollis - askewi by a lot of features which are just partly discussed here. Although a few species share some morphological characters with M. askewi sp. nov., especially in having antennae with three anelli and pronotum with long collar, they can be well differentiated from this species and are probably not closely allied to it. Mesopolobus szelenyii Bouček, 1974 have three anelli and the pronotal collar is a little more than one-fifth the length of mesoscutum (0.18x), but the collar is carinate anteriorly in its middle part, the head is 1.25-1.28x as broad as mesoscutum (1.11-1.16x in askewi) and the fore wings have fuscous cross-fascia attached to darker parastigma (hyaline in askewi). Mesopolobus blascoi Askew, 1994, which was later synonymised under M. maculipennis (Mercet) by
Two mitochondrial sequences were obtained in total. The COI amplicon (663 bp) was successfully sequenced using only the forward primer, while the CYTB amplicon (756 bp) was sequenced with both the forward and reverse primers. The COI sequence showed a difference of 45 base pairs compared to the Mesopolobus amaenus (Walker, 1834) sequence recorded in GenBank, while the CYTB sequence differed by 91 base pairs from Pteromalus puparum (Linnaeus, 1758). Both unique sequences were uploaded to the GenBank database under accession numbers PQ331194 for COI and PQ342001 for CYTB.
Тhe species collected during the present study belong mostly to the family Pteromalidae, with the exception of A. vulgaris, which was recently classified as Asaphesinae incertae sedis in Chalcidoidea (
The collected species have various host preferences within different insect groups. They are mostly larval ectoparasitoids and only S. micans has been proposed as a probable larval endoparasitoid of the Barley Gout-fly, Chlorops taeniopus Meigen (
The three Mesopolobus species have different host associations, but a certain similarity is known for M. dubius and M. tibialis, which are parasitoids in galls of Cynipidae (Hymenoptera, Cynipoidea) on various Quercus species. However, two records of M. dubius associated with the invasive gall-wasp Dryocosmus kuriphilus Yasumatsu (Hymenoptera, Cynipidae) on the sweet chestnut Castanea sativa Mill. have also been published in the past (
The host of the four Trichomalus species are quite different, both in biological and ecological aspects. Three of them, T. bracteatus, T. helvipes and T. perfectus, prefer to parasitise stem-boring larvae living in grasses, while T. inscitus is an oligophagous ectoparasitoid mostly of the flea weevils belonging to genus Orchestes and rarely of other curculionids such as Rhamphus, Rhynchaenus and Stereonychus associated with various tree hosts (
Considering published data on the biology of the species discussed above, it is surprising to find them associated with P. abies. This statement is definitely clear for species like M. dubius and M. tibialis, whose trophic relationships mostly include hosts on oaks, for M. morys which attacks weevils’ larvae in Brassicaceae grass plants and for all Trichomalus spp. having in mind their known hosts living on grasses or deciduous trees. A possible association with conifers has been recorded only for A. vulgaris and M. tibialis with Pinus halepensis Mill. (
In this study, a great number of jumping plant-lice belonging to the psyllid genus Cacopsylla (Hemiptera, Psyllidae) were collected from the lower branches of the Norway spruce in most of the sampling sites. These insects, as well as all Psyllidae, are well known honeydew producers. Their immature to adult life cycle is restricted to one or a few closely-related host-plant species (
Therefore, acknowledging the biology of the discussed chalcidoids and the attraction of many Pteromalidae to honeydew produced by hemipterans (aphids) (
We express our gratitude to Dr. Ilia Gjonov and Monica Pramatarova (PhD student) (Faculty of Biology, Sofia University "St. Kliment Ohridski", Bulgaria) for the identification of the psyllid material.
This study was supported by the grant DN11/13–18.12.2017 (Biodiversity of families Eulophidae and Pteromalidae (Hymenoptera, Chalcidoidea) in mountainous habitats. Barcoding and distinguishing of close species), funded by the Bulgarian National Science Fund (BNSF) of the Ministry of Education and Science of Bulgaria.
All specimens used in this work were digitised as part of the project DiSSCo-BG (Upgrade of the Research Infrastructure “Distributed System of Scientific Collections – Bulgaria”) funded by the National Roadmap for Research Infrastructures, Ministry of Education and Science of the Republic of Bulgaria.
Ivaylo Todorov - Conceptualisation, Methodology, Investigation, Data Curation, Writing - Original draft, Visualisation, Supervision, Funding Acquisition.
Mircea-Dan Mitroiu - Validation, Investigation, Data Curation, Writing - Review and Editing.
Aneliya Bobeva - Methodology, Validation, Investigation, Data Curation, Writing - Original draft, Writing - Review and Editing.
Peter Boyadzhiev - Methodology, Validation, Investigation, Data Curation, Writing - Review and Editing.