No abstract

The Platygastroidea comprises two families of parasitoids, Scelionidae and Platygastridae, and nearly 4500 described species. They parasitize a diverse array of insects as well as spiders. Idiobiont endoparasitism of eggs is the putative ground plan biology, as reflected by all scelionids, but most Platygastridae are koinobiont endoparasitoids of immature Auchenorrhyncha, Sternorrhyncha, and Cecidomyiidae. The superfamily is demonstrably monophyletic but its phylogenetic position remains uncertain. Relationships within the Platygastroidea are also poorly known and the group is in need of comprehensive phylogenetic study. Significant information is available on host relationships and biology, although much of this is biased to a few genera of Telenominae that are employed as biocontrol agents. Hosts for many genera are unknown, in particular those that inhabit leaf litter or parasitize solitary host eggs. The Trissolcus basalis-Nezara viridula parasitoid-host association has become a favored model system in ecological, behavioral, and physiological research on insects.

The skeletomusculature of the head and mesosoma of the parasitoid wasp family Scelionidae is reviewed. Representatives of 27 scelionid genera are examined together with 13 non-scelionid taxa for comparison. Terms employed for other groups of Hymenoptera are reviewed, and a consensus terminology is proposed. External characters are redescribed and correlated with corresponding apodemes, muscles and putative exocrine gland openings; their phylogenetic importance is discussed. 229 skeletal structures were termed and defined, from which 84 are newly established or redefined. 67 muscles of the head and mesosoma are examined and homologized with those present in other Hymenoptera taxa. The presence of the cranio-antennal muscle, an extrinsic antennal muscle originating from the head capsule, is unique for Scelionidae. The dorsally bent epistomal sulcus and the corresponding internal epistomal ridge extend to the anterior margin of the oral foramen, the clypeo-pleurostomal line is absent and the tentorium is fused with the pleurostomal condyle. The frontal ledge is present in those scelionid genera having the anterior mandibular articulation located on the lateral margin of the oral foramen. The ledge corresponds to the site of origin of the mandibular abductor muscle, which is displaced from the genal area to the top of the frons. The protractor of the pharyngeal plate originates dorsally of the antennal foramen in Scelionidae. All scelionid genera have a postgenal bridge developed between the oral and occipital foramina. The propleural arm is reduced, muscles originating from the propleural arm in other Hymenoptera are situated on other propectal structures in Scelionidae. The profurcal bridge is absent. The first flexor of the fore wing originates from the posteroventral part of the pronotum in Scelionidae and Vanhorniidae, whereas the muscle originatesfrom the mesopleuron in all other Hymenoptera. The netrion apodeme anteriorly limits the site of origin of the first flexor of the fore wing. Three types of netrion are described on the basis of the relative position of the netrion apodeme and the posterior pronotal inflection. The occlusor muscle apodeme is absent in basal Scelionidae, the fan-shaped muscle originates from the pronotum. In Nixonia the muscle originates posterior to the netrion apodeme. The skaphion apodeme crosses the site of origin of the longitudinal flight muscle. The lateral and dorsal axillar surfaces and the axillar carina are defined and described for the first time in Platygastroidea. The retractor of the mesoscutum is reported in Scelionidae and the variability of the muscle and corresponding skeletal structures within the family is described. The term sternaulus is redefined on the basis of the site of origin of the mesopleuro-mesobasalare muscle. The term speculum is adopted from Ichneumonidae and Cynipoidea taxonomy on the basis of the site of origin of the mesopleuro-mesofurcal muscle. The remnants of the mesopleural ridge, sulcus and mesopleural arm and pit and the putative border between the mesepisternum and mesepimeron is discussed. The mesopleural depressor of the mesotrochanter sensu Gibson 1985 originates from the anterior extension of the mesofurca and therefore the muscle is redefined and referred to in the present study as the lateral mesofurco-mesotrochanteral muscle. In Nixonia, Sparasion, Idris and Gryon both the lateral and median mesofurco-mesotrochanteral muscles are present. The lateral mesofurco-mesotrochanteral muscle is present in Platygastridae. The second flexor of the hind wing at least partly originates from the posteriorly delimited area of the mesopectus in Scelionidae similarly to some other Proctotrupomorpha and Chalcidoidea. The serial homology of this area and the netrion is discussed. The possible serial homology of the medially elevated area of the metanotum and mesoscutellum and the usage of the term metascutellum in Apocrita is discussed with the descriptions of correlated internal structures. The anterior metanotal wing process is located on the independent humeral sclerite in Scelionidae, similar to other Apocrita except Cynipoidea. The metanotal depressor of the metatrochanter originates from the humeral sclerite in Scelionidae as well as in some other Proctotrupoidea. The metapleuron is extended secondarily dorsally of the metapleural ridge and corresponding metapleural sulcus in Scelionidae. In Telenominae, Gryonini and Baeini the metafurca is located posteriorly on the metadiscrimenal lamella.

The concept of semantic tagging and its potential for semantic enhancements to taxonomic papers is outlined and illustrated by four exemplar papers published in the present issue of ZooKeys. The four papers were created in different ways: (i) written in Microsoft Word and submitted as non-tagged manuscript (doi: 10.3897/zookeys.50.504); (ii) generated from Scratchpads and submitted as XML-tagged manuscripts (doi: 10.3897/zookeys.50.505 and doi: 10.3897/zookeys.50.506); (iii) generated from an author’s database (doi: 10.3897/zookeys.50.485) and submitted as XML-tagged manuscript. XML tagging and semantic enhancements were implemented during the editorial process of ZooKeys using the Pensoft Mark Up Tool (PMT), specially designed for this purpose. The XML schema used was TaxPub, an extension to the Document Type Definitions (DTD) of the US National Library of Medicine Journal Archiving and Interchange Tag Suite (NLM). The following innovative methods of tagging, layout, publishing and disseminating the content were tested and implemented within the ZooKeys editorial workflow: (1) highly automated, fine-grained XML tagging based on TaxPub; (2) final XML output of the paper validated against the NLM DTD for archiving in PubMedCentral; (3) bibliographic metadata embedded in the PDF through XMP (Extensible Metadata Platform); (4) PDF uploaded after publication to the Biodiversity Heritage Library (BHL); (5) taxon treatments supplied through XML to Plazi; (6) semantically enhanced HTML version of the paper encompassing numerous internal and external links and linkouts, such as: (i) vizualisation of main tag elements within the text (e.g., taxon names, taxon treatments, localities, etc.); (ii) internal cross-linking between paper sections, citations, references, tables, and figures; (iii) mapping of localities listed in the whole paper or within separate taxon treatments; (v) taxon names autotagged, dynamically mapped and linked through the Pensoft Taxon Profile (PTP) to large international database services and indexers such as Global Biodiversity Information Facility (GBIF), National Center for Biotechnology Information (NCBI), Barcode of Life (BOLD), Encyclopedia of Life (EOL), ZooBank, Wikipedia, Wikispecies, Wikimedia, and others; (vi) GenBank accession numbers autotagged and linked to NCBI; (vii) external links of taxon names to references in PubMed, Google Scholar, Biodiversity Heritage Library and other sources. With the launching of the working example, ZooKeys becomes the first taxonomic journal to provide a complete XML-based editorial, publication and dissemination workflow implemented as a routine and cost-efficient practice. It is anticipated that XML-based workflow will also soon be implemented in botany through PhytoKeys, a forthcoming partner journal of ZooKeys. The semantic markup and enhancements are expected to greatly extend and accelerate the way taxonomic information is published, disseminated and used.

No abstract

Trissolcus japonicus (Ashmead) and T. cultratus (Mayr), comb. rev. are under study as classical biological agents to control the brown marmorated stink bug Halyomorpha halys (Stål) in North America. Here we present diagnoses for all Nearctic species of Trissolcus, including T. japonicus and T. cultratus comb. rev., and identification keys to enable separation of these species from the existing fauna. Trissolcus cultratus comb. rev. is removed from synonymy with T. flavipes. Two new species are described, Trissolcus valkyria sp. n. and T. zakotos sp. n. A neotype is designated for T. brochymenae and a lectotype is designated for T. basalis.

An updated classification of the order Hymenoptera is provided with the current numbers of genera and species described so far specified. The order is composed of 2 suborders, 27 superfamilies, 132 families, 8423 extant genera with an additional 685 extinct genera. Considered one of the most species-rich insects orders a total of 153088 extant species have been described, in addition to 2429 extinct species.

Abstract. Parasitoid wasps of the subfamily Telenominae (Hymenoptera: Platygastroidea, Platygastridae) develop as immatures within the eggs of other insects (Lepidoptera, Hemiptera, Diptera and Neuroptera). Rearing records indicate that individual species are restricted to attack hosts within only one of these four main groups. We conducted a phylogenetic analysis of the group using sequence data from multiple genes (18S , 28S , COI , EF-1α) to assess the pattern of shifts among host groups and to test the monophyly of and relationships among genera and species-groups. Telenominae sensu Masner -that is, including only the nominate tribe Telenomini -is not monophyletic. Representatives of the Psix group of genera (Psix Kozlov & Lê and Paratelenomus Dodd) form a monophyletic group that is sister to Gryon Haliday (Scelioninae: Gryonini) and are excluded from the subfamily. The remaining telenomines are monophyletic. The genus Phanuromyia Dodd and the crassiclava group of Telenomus Haliday, both recorded as parasitoids of planthopper eggs (Hemiptera: Auchenorrhyncha, Fulgoroidea), form a monophyletic group that is sister to all other telenomines exclusive of the Psix group. Twenty-nine species of the crassiclava and aradi groups of Telenomus are transferred to Phanuromyia as new combinations. Basal elements of the remaining species are all in groups reared from the eggs of true bugs (Heteroptera), primarily the stink bugs (Pentatomoidea) and seed bugs (Lygaeoidea). A shift to parasitism of lepidopteran eggs evolved within a single clade, occurring either one or two times. From this clade a small group of species, the Telenomus tabanivorus group, subsequently shifted to parasitism of egg masses of true flies (Tabanidae and Stratiomyiidae). Aholcus Kieffer and Platytelenomus Dodd both belong to the clade of lepidopteran parasitoids and are considered as junior synonyms of Telenomus (new synonymy for Aholcus). The monophyletic status of the two core genera, Telenomus and Trissolcus could not be resolved using these data. The phylogenetic pattern of host shifts suggests comparisons among taxa that may be fruitful in elucidating mechanisms by which parasitoids locate their hosts, the proximate factors that determine the host range, and the changes in these factors that influence host changes.