Type specimens of the Hymenoptera Symphyta described by V. M. Ermolenko and deposited in the collection of the I. I. Schmalhausen Institute of Zoology,the National Academy of Sciences of Ukraine (Kiev)

A list of type specimens of 20 species of 18 genera belonging to 5 sawfly families (Cimbicidae, Tenthredinidae, Pamphiliidae, Xiphydriidae, and Cephidae), described by V. M. Ermolenko, is presented.     

Morphology of the pretarsus of the sawflies and horntails (Hymenoptera: 'Symphyta')

The pretarsal structures have been studied in representatives of 13 families of 'Symphyta' by means of light microscopy. The pretarsal sclerites (manubrium, planta, and unguitractor) vary in shape among different families. The shape of the manubrium is triangular in representatives of Xyelidae and Orussidae and bifurcated in those of Tenthredinoidea. For representatives of Siricomorpha, an elongated shape of the manubrium is typical with such variations, as distally expanded, proximally expanded, clavate, spear-shaped. Plantae of different Symphyta vary in shape and level of sclerotization. In representatives of Siricidae, the female manubrium and arolium are significantly reduced, and arcus and dorsal plates are completely absent. Siricid males possess all pretarsal sclerites and a well-developed arolium. Auxiliary sclerites are absent in representatives of Orussidae. Trichoid sensilla are absent on the plantae in representatives of Cephidae and Orussidae. Other studied Symphyta possess two trichoid sensilla on the planta. Representatives of all investigated families bear two campaniform sensilla on the manubrium, with the exception of Siricidae having three sensilla. Kinematics of the pretarsus with bifurcated manubrium are modeled and discussed.     

The phylogeny of lower Hymenoptera (Insecta), with a summary of the early evolutionary history of the order

A cladistic analysis of the lower Hymenoptera, including all the ‘symphytan’ families and the apocritan families Stephanidae, Megalyridae, Trigonalyidae, Ibaliidae, Vespidae and Gasteruptiidae, has been undertaken. A total of 98 characters were scored for 21 taxa. Twenty equally parsimonious minimum-length trees were obtained. The phylogenetic status of the Xyelidae is uncertain: they might be monophyletic. or the Xyelinae might be the sistergroup of the rest of the Hymenoptera. The non-xyelid Hymenoptera are probably monophyletic; the phylogeny Tenthredinoidea + (Megalodontoidea + (Cephidae + (Anaxyelidea + (Siricidae + (Xiphydriidae + (Orussidae + Apocrita)))))) is proposed for this clade. The Blasticotomidae are probably the sistergroup of all othe Tenthredinoidea, but tenthredinoid phylogeny is otherwise uncertain. Substantial homoplasy occurs within the ‘siricoid’ families, making the relative positions of the Anaxyelidae and Siricidae uncertain. The Stephanidae might be the sistergroup of the rest of the Apocrita; the phylogeny of the remaining apocritan taxa included is insufficiently elucidated. The phylogeny proposed here supports the hypothesis that the appearance of parasitism in the Hymenoptera took place in the common ancestor of Orussidae + Apocrita, the host of which was probably wood boring insect larvae. The exact larval mode of feeding of the ancestral hymenopteran cannot be determined due ot the diversity of lifestyles in the basal lineages of the order.     

Phylogeny and classification of the extant basal lineages of the Hymenoptera (Insecta)

The phylogeny of the basal hymenopteran lineages, including representatives of all ‘symphytan’ families, is anal; In total, 236 morphological characters were scored for 44 exemplars, including six outgroup, two xyelic tenthredinoid, five pamphilioid, three cephoid, five ‘siricoid’, one orussid, and six apocritan taxa. The datas analysed with parsimony under equal weights and under implied weights. The monophyly of the Hymenopte strongly supported but the sistergroup of the Hymenoptera cannot be identified with confidence. The relations of the ‘symphytan’ lineages are Xyeloidea +(Tenthredinoidea+ (Pamphilioidea + (Cephoidea + (Ariaxyelic (Siricidae + (Xiphydriidae +(Orussoidea+Apocrita))))))). Many of the relationships between the superfamilies, especially in the basal branching pattern, are only weakly corroborated. The monophyly of most superfamilies is supported, and all may be monophyletic except the ‘Siricoidea’, which is clearly paraphyletic. It is difficult to di whether the Siricidae or the Anaxyelidae are the closest relatives of Xiphydriidae + (Orussoidea + Apocrita). support for the sistergroup relationship between the Orussoidea and the Apocrita is substantial, putative apomorphies being provided by most character systems. There is also good evidence in favour of the monophj the Apocrita. The internal phylogeny of the Tenthredinoidea differs considerably from the results of earlier anal The Blasticotomidae are the sistergroup of the Tenthredinoidea s.s. Relationships at the base of the Tenthredini s.s. are weakly supported. It is uncertain whether the Tenthredinidae are monophyletic or comprise a 1 paraphyletic grade within the Tenthredinoidea s.s. The Diprionidae may be the sistergroup to Cimbicidae +(Argidae+ Pergidae). Most relationships within the Cimbicidae + (Argidae + Pergidae) clade are corroborated, with the exception of the monophyly of the Argidae. It is proposed to elevate the Anaxyelidae the Xiphydriida both to superfamily status. The family‐level classification of the Tenthredinoidea will probably have to be changed, but this must await further clarification of the phylogeny of this superfamily.     

Before the wasp-waist: comparative anatomy and phylogenetic implications of the skeleto-musculature of the thoraco-abdominal boundary region in basal Hymenoptera (Insecta)

The skeleto-musculature of the metathorax and first abdominal segment was studied in representatives from all ’symphytan’ families. Forty-three informative characters were coded and scored. The distribution of character states are discussed with reference to recent cladistic treatments of the Hymenoptera. Previously unreported autapomorphies for the Hymenoptera are the separation of the metathoracic trochantins from the metepisterna and metacoxae, the position of the metafurca anteriorly on the discrimenal lamella of the metathorax and the presence of second abdominal sternum (S2)-metacoxal muscles. The absence of metapleuro-S2 muscles is an autapomorphy for the non-xyelid Hymenoptera. Putative autapomorphies of the Tenthredinoidea are: (1) the presence of transverse metanotal muscles, (2) the subdivision of the second phragmo-third phragmal muscles, part of which arises from the metalaterophragmal lobes, (3) the posterior thoracic spiracle occlusor muscles arising from the mesepisterna, (4) the absence of trochantins and metanoto-trochantinal muscles and (5) the presence of elongate lateral metafurcal arms. Having the paracoxal sulci extending along the anterior margins of the metepisterna and the anterior metafurcal arms reduced are synapomorphies for all tenthredinoid families excluding Blasticotomidae. The presence of transversely extended cenchri with hooks on their entire surface is a putative synapomorphy for Diprionidae + Cimbicidae + Argidae + Pergidae. The clade Cimbicidae + Argidae + Pergidae is supported by the absence of metanoto- metabasalar muscles, the fusion of the first abdominal tergite (T1) with the metepimera and the absence of posterior metapleuro-metafurcal muscles. Autapomorphies of the Cimbicidae are the absence of the metalaterophragmal lobes and the metalaterophragmal-metafurcal muscles. Having the mesoscutello-metanotal muscle inserting on a projection from the anterior margin of the metanotum, surrounding the tendon with sclerotised cuticle, is a synapomorphy for the Argidae and Pergidae. Autapomorphies of the Cephoidea are the absence of cenchri, the presence of distinct articulations between T1 and the metepimera, and having the paracoxal sulci extending subparallel with the metafurcal discrimen. The monophyly of the Siricidae is supported by the absence of the anapleural clefts and the presence of an elongate mesospina projecting posteriorly between the anterior metafurcal arms. The presence of a membranous pouch ventrally of T1 and of large T1-metafurcal muscles is unique to Xiphydria camelus among the taxa examined. The absence of hind wing tegulae, posterior metapleuro-metafurcal, metanoto-trochantinal and anterior metanoto-metacoxal muscles, and the presence of elongate lateral metafurcal arms are synapomorphies for Xiphydriidae + Orussidae + Apocrita. The Orussidae greatly resembles the Apocrita in the region studied, a synapomorphy for the two taxa being the presence of metepisternal depressions. An autapomorphy for the Apocrita is the fusion of T1 with the metapleural arms; these structures closely abut in Orussidae. The fusion of T1 with the metepimera was preceded by the reduction of the posterior parts of the metepimera, as observed in Anaxyelidae, Xiphydriidae, and Orussidae. This makes the lines of fusion between T1 and the metepimera confluent with the metapleural sulci in the Apocrita. There is no compelling evidence for considering the configuration of T1 and the metepimera in Cephoidea to be incipient in the formation of the propodeum in Apocrita. The close association between the meso- and metathorax and the integration of T1 in the metathorax evolved gradually twice within the basal hymenopteran lineages, culminating in the Apocrita and the Cimbicidae + Argidae + Pergidae clade. Accepted: 2 September 1999     

On the edge of parasitoidism: a new Lower Cretaceous woodwasp forming the putative sister group of Xiphydriidae + Euhymenoptera

The fossil woodwasp Cratoenigma articulata gen. et sp.n. (Insecta: Hymenoptera) is described from the Lower Cretaceous Crato formation of Brazil. This fossil cannot be placed in any existing superfamily, but its putative phylogenetic position within Hymenoptera is discussed in detail on the basis of relevant thoracic, abdominal and wing venation characters. These characters are critically evaluated and compared with those of extant and fossil Hymenoptera. The phylogenetic position of C. articulata sp.n. is investigated relative to extant Xyelidae, Tenthredinoidea s.l., Pamphilioidea, Cephidae, Siricoidea, Xiphydriidae, Orussidae and Apocrita, and also to Mesozoic Gigasiricidae, Myrmiciidae, Daohugoidae, Sepulcidae, Anaxyelidae, Paroryssidae and Ephialtitidae. Based on the presence of a synapomorphic transscutal articulation, a plesiomorphic unconcealed mesopostnotum and autapomorphic hindwing venation (cu‐a distinctly basal to fork between M and Cu), C. articulata sp.n. most likely forms the sister group of Xiphydriidae + Euhymenoptera. This would place it well within Unicalcarida, i.e. the clade in which the transition from endophytic to parasitoid lifestyle evolved.     

Phylogeny of the symphytan grade of Hymenoptera: new pieces into the old jigsaw(fly) puzzle

The Hymenoptera constitutes one of the largest, and ecologically and economically most important, insect orders. During the past decade, a number of hypotheses on the phylogenetic relationships among hymenopteran families and superfamilies have been presented, based on analyses of molecular and/or morphological data. Nevertheless, many questions still remain, particularly concerning relationships within the hyperdiverse suborder Apocrita, but also when it comes to the evolutionary history of the ancestrally herbivorous “sawfly” lineages that form the basal, paraphyletic grade Symphyta. Because a large part of the uncertainty appears to stem from limited molecular and taxonomic sampling, we set out to investigate the phylogeny of Hymenoptera using nine protein‐coding genes, of which five are new to analyses of the order. In addition, we more than tripled the taxon coverage across the symphytan grade, introducing representatives for many previously unsampled lineages. We recover a well supported phylogenetic structure for these early herbivorous hymenopteran clades, with new information regarding the monophyly of Xyelidae, the placement of the superfamily Pamphilioidea as sister to Tenthredinoidea + Unicalcarida, as well as the interrelationships among the tenthredinoid families Tenthredinidae, Cimbicidae, and Diprionidae. Based on the obtained phylogenies, and to prevent paraphyly of Tenthredinidae, we propose erection of the tribe Heptamelini to family status (Heptamelidae). In particular, our results give new insights into subfamilial relationships within the Tenthredinidae and other species‐rich sawfly families. The expanded gene set provides a useful toolbox for future detailed analyses of symphytan subgroups, especially within the diverse superfamily Tenthredinoidea.     

Simultaneous analysis of basal Hymenoptera (Insecta): introducing robust-choice sensitivity analysis

Molecular characters are analysed on their own and in combination with morphological data to examine the phylogenetic relationships of the basal lineages of Hymenoptera ('Symphyta'). This study covers 47 sawfly genera and nine apocritan families and includes molecular sequences from five genes − 12S, 16S, 18S and 28S ribosomal genes and cytochrome oxidase 1 − as well as 343 morphological characters. A robust-choice sensitivity analysis is performed with the data. First, the simultaneous analysis is repeated three times, each time employing a different step matrix for weighting the transformations of the molecular characters. Then, the results of all three simultaneous analyses are summarized in a strict consensus in order to avoid basing the conclusions on a narrow set of assumptions. This methodology is discussed in the paper. The relationships among superfamilies largely confirm previous hypotheses, being (Xyeloidea (Tenthredinoidea s.l. (Pamphilioidea (Cephoidea (Siricoidea (Xiphydrioidea (Orussoidea Apocrita))))))), where Siricoidea is understood as Siricidae+Anaxyelidae. However, the relationships within Tenthredinoidea s.s. proposed here are novel: ({Argidae Pergidae}[ Athalia {(Diprionidae Cimbicidae) Tenthredinidae minus Athalia }]).  © 2003 The Linnean Society of London . Biological Journal of the Linnean Society , 2003, 79, 245–275.     

Checklist of the species of the aseptate gregarine families Aikinetocystidae,Diplocystidae, Allantocystidae,Schaudinnellidae, Ganymedidae,and Enterocystidae

The genera and species in six families of the eugregarine suborder Aseptatorina Chakravarty, 1960, are reviewed and the presently accepted ones are listed: Aikinetocystidae Bhatia, 1930 (two genera and two species); Diplocystidae Bhatia, 1930 (one genus and eight species); Allantocystidae tocystidae Bhatia, 1930 (one genus and one species); Schaudinnellidae Poche, 1913 (one genus and one species); Ganymedidae Huxley, 1910 (one genus and one species); and Enterocystidae Codreanu, 1940 (one genus and eight species). A list of 22 synonyms and lapsi calami is also given. Species which might be of value in the biological control of disease vectors are indicated.     

Mouthpart evolution in adults of the basal, 'symphytan', hymenopteran lineages

We review feeding biology and mouthpart structure generally among adults of the basal hymenopteran, or ‘symphytan’, lineages (sawflies, woodwasps, horntails and their relatives). These insects feed on a wide range of materials: floral and extrafloral nectar, pollen, plant (floral and leaf) tissues, plant (angiosperm) sap, the juice of ripe fruit, die spermatial fluid of rust fungi, sternorrhynchan bug honeydew, and insect tissues. Adults show feeding‐related mouthpart specialization either for consuming pollen (the Xyelidae only) or for consuming ‘concealed’ floral nectar (several families). Seven functional types of elongated proboscis or ‘concealed‐nectar extraction apparatus (GNEA)’ have previously been recognized among Hymenoptera. We identify an additional type, which appears to be unique among Hy‐menoptera and has probably evolved direcdy from unspecialized mouthparts (labiomaxillary complex). In total, three types of CNEA are known to occur in ‘Symphyta’. Type 1 occurs in Pamphiliidae, Megalodontesidae, Argidae, Pergidae, Tenthredinidae, Cimbicidae and Cephidae. Type 5 occurs in Pergidae (in two unidentified species of Euryinae). Type 8 occurs in Tenthredinidae (in the genus Nipponorhynchus Takeuchi). CNEA of some type or other has arisen at least twice within the family Tenthredinidae and at least twice widiin die pergid subfamily Euryinae. Evolutionary parallelism in CNEA structure has occurred between the basal, ‘symphytan’, hymenopteran lineages and die Apocrita, a phenomenon hitherto not mentioned in the literature. Within the ‘Symphyta’, possession of Type 1 CNEA appears to be a ground plan feature of each of the following taxa: the pergid genus Eurys Newman, the megalodontesid genus Megalodontes Latreille (the only extant representative of the Megalodontesidae) and the tenthredinid genus Cuneala Zirngiebl, while possession of Type 8 appears to be a ground plan feature of die tenthredinid genus Mpponorhynchus Takeuchi. However, in general among ‘Symphyta’, possession of CNEA is characteristic of only small and taxonomically subordinate groups, suggesting that CNEA has evolved independendy many times within the basal hymenopteran lineages rather than being inherited from a common ancestor early in the evolutionary history of the Hymenoptera. In other words, ecological expediency radier than phylogenetic history mainly accounts for its distribution pattern within the basal lineages. The results of a morphological survey of ‘Symphyta’ indicate that the habit of exploiting ‘concealed nectar’, by means of CNEA, is fairly     

Composition and age of the Daohugou hymenopteran (Insecta, Hymenoptera = Vespida) assemblage from Inner Mongolia, China

Hymenopteran fossils from Daohugou, Inner Mongolia, China are assigned to 17 families. These include, in decreasing order of importance, Ephialtitidae, Xyelidae, Siricidae, Xyelydidae, Anaxyelidae, Karatavitidae s.l ., Mesoserphidae, Megalyridae and Praeaulacidae. Analysis of the taxonomic composition suggests that the assemblage is of Mid Jurassic age. The rather low abundance of Xyelidae suggests that the climate in Daohugou during the Mid Jurassic might have been thermally intermediate between that of peri-Baikal Siberia during the Early/Mid Jurassic transition and southern Kazakhstan during the early Late Jurassic. A new family, Protosiricidae fam. nov., is established herein and the family Gigasiricidae is reduced in rank to Gigasiricinae and referred to the Siricidae.     

中国两栖、爬行动物更新名录

本文在2015年发表的爬行动物名录及同年《中国两栖类信息系统》发布的两栖动物名录的基础上, 通过整理新发表的分类学研究及先前名录遗漏的部分早期文献, 更新了截至2019年底中国现生本土两栖、爬行动物物种名录。2015-2019年间, 中国两栖动物新记录1科, 新描述2属, 恢复1属有效性, 新记录1属, 新描述或恢复有效种74种, 新增国家纪录18种; 另6属、8种的有效性未得到近年研究证据支持(在此视为次定同物异名而未做收录, 后同)。同期, 中国爬行动物新恢复5科, 新描述1亚科, 新描述1属, 恢复3属有效性, 新记录3属, 新描述、恢复或提升有效种43个, 新增国家纪录10种; 另有5属、4种的有效性未得到近年研究证据支持, 并移除1属、4种在我国的分布纪录。此外, 通过整理2015年前文献, 爬行动物增补3属, 提升3亚种至种级地位, 增补国家新纪录3种, 另有3属、2种的有效性未得到近年研究证据支持, 同时移除1种在我国的分布纪录。综上, 截至2019年底, 我国共记录现生本土两栖动物3目13科62属515种(蚓螈目1科1属1种, 有尾目3科14属82种, 无尾目9科47属431种), 爬行动物3目35科135属511种(鳄形目1科1属1种, 龟鳖目6科18属34种, 有鳞目蛇亚目18科73属265种、蜥蜴亚目10科43属211种)。此外, 本文还对先前名录中部分爬行动物的中文名提出了修改建议, 建议恢复部分物种的惯用中文名。2015-2019年, 新物种及新纪录已知物种数量占现两栖、爬行动物物种总数的17.1%和10.2%。近年来, 我国发表的两栖、爬行动物新物种和已知物种的新纪录数量持续增加, 分类体系也在研究中不断完善, 建议今后及时地进行阶段性总结, 同时对存在的问题提出讨论, 以推动中国两栖、爬行动物分类学研究工作的进一步开展。     

Sperm structure and ultrastructure in the Hymenoptera (Insecta)

A light and electron microscopical survey of spermatozoan gross morphology and ultrastructure in the Hymenoptera is presented. Details are provided for the first time for members of the families Xyelidae, Argidae, Tenthredinidae, Diprionidae, Cephidae, Figitidae, Proctotrupidae, Diaprii- dae, Heloridae, Eurytomidae, Leucospidae, Perilampidae, Torymidae, Braconidae, Dryinidae, Sphecidae, Pompilidae and Vespidae. Spermatozoan length ranged from 8 μ m in some Braconidae to 500 μm in one chalcidoid. Considerable variation in gross morphology and ultrastructure were observed between taxa. Several phylogenetically informative characters were noted. Very small spermatozoa characterized most of the non-cyclostome subfamilies of Braconidae; spirally twisted axoneme and mitochondrial derivatives occur in the Eulophidae, Eurytomidae and Pteromalidae; spermatozoa with virtually indistinguishable head (nucleus and acrosome) regions characterized the Vespinae and Polistinae. The presence of well-developed spermatodesmata in the vas deferens and seminal vesicle characterize the Symphyta and were largely absent from other groups though they are occasionally present in some bees.     

Updated taxonomic list and conservation status of chondrichthyans from the exclusive economic zone of Venezuela,with first generic and specific records

Using the last taxonomic review of chondrichthyans of the world, we selected the species distributed in the north-western Atlantic Ocean (NWA) and compared it with the available published literature related to the class Chondrichthyes in the Venezuelan exclusive economic zone. We also revised information from worldwide databases such as: FAO (NWA-31 area), GBIF, iSpecies, IUCN and OBIS, as well as available museum collection databases. The taxonomic validity was checked using the Catalogue of Fishes of the California Academy of Sciences and recent references. The past published Venezuelan lists of chondrichthyans combined included nine orders, 30 families and 108 species. The updated list with 12 orders, 36 families and 122 species increased by three new orders, six families, three shark genera, nine shark species (one replacing another species), one chimaera genus, two chimaera species, three batoid genera and six batoid species (two replacing other species). Four holotype specimens (two sharks and two rays) are deposited in Venezuelan Museums. Most of the species have an IUCN conservation status, including four species catalogued as Critically Endangered, six as Endangered and 18 species as Vulnerable. Deep-sea fisheries, scientific exploration and taxonomic/genetic revisions might add future increments to the Venezuelan chondrichthyan list.     

Simultaneous analysis of the basal lineages of Hymenoptera (Insecta) using sensitivity analysis

The first simultaneous analysis of molecular and morphological data of basal hymenopterans that includes exemplars from all families is presented. DNA sequences (of approximately 2000–2700 bp for each taxon) from the nuclear genes 18S and 28S and the mitochondrial genes 16S and CO1 have been sequenced for 39 taxa (four outgroup taxa, 29 symphytans, and six apocritans). These DNA sequences and 236 morphological characters from Vihelmsen [Zool. J. Linnean Soc. 131 (2001) 393] were analyzed separately as well as simultaneously. All analyses were performed on unaligned sequences, using the optimization alignment (= direct optimization) method. Sensitivity analysis sensu Wheeler [Syst. Biol. 44 (1995) 321] was applied by analyzing the data under nine different combinations of analysis parameter values. The superfamily level relationships of basal hymenopterans as proposed by Vilhelmsen [Zool. J. Linnean Soc. 131 (2001) 393] and Ronquist et al. [Zool. Scr. 28 (1999) 13] are mostly confirmed, except that Pamphilioidea is the sister group to Tenthredinoidea s.l. and that Anaxyelidae (i.e., Syntexis libocedrii) and Siricidae are supported as a monophyletic group, partly reestablishing the traditional concept of Siricoidea. The resulting hypothesis that best represents the combined evidence from morphology and DNA sequences is (Xyeloidea (Tenthredinoidea s.l. Pamphilioidea) (Cephoidea (Siricoidea (Xiphydrioidea (Orussidae Apocrita))))), with Siricoidea = Anaxyelidae +Siricidae. The phylogenetic system within Tenthredinoidea s.l., derived from the combined evidence, is (Blasticotomidae (Tenthredinidae including Diprionidae (Cimbicidae (Argidae Pergidae)))).     

Review of morphological evidence on the phylogeny of basal Hymenoptera (Insecta), with a discussion of the ordering of characters

In a previous study of the phylogeny of basal Hymenoptera, Vilhelmsen (2001; Zool. J. Linn. Soc . 131 : 393–442) compiled an extensive morphological data matrix for a phylogenetic analysis of basal Hymenoptera, comprising 38 hymenopteran genera. In this study, his characters are revised. This results in a cladogram whose relationships largely agree with those proposed by Vilhelmsen, except that the relationships at the base of the Hymenoptera are unresolved. The revised data matrix is expanded by 17 sawfly and three apocritan taxa. Moreover, 112 new morphological characters from different parts of the larval and adult morphology are also added to the data matrix, including 82 from a recent study of the terminal abdominal segments of male Hymenoptera. The addition of the new characters leads to Xyelidae, again, being the sister-group of all other Hymenoptera. The relationships among the sawfly families as proposed by Vilhelmsen are confirmed, except that the relationships among Syntexis , Siricidae and Xiphydriidae + Vespina are unresolved and that the monophyly of Apocrita is not convincingly supported. A separate analysis is performed which includes all extant genera of Xyelidae. The internal phylogeny of Xyelidae is determined as (( Macroxyela Megaxyela ) Xyelecia ( Xyela Pleroneura )).  © 2003 The Linnean Society of London, Biological Journal of the Linnean Society , 2003, 79 , 209–243.     

Taxonomic studies of the Halosphaeriaceae: Corollospora Werdermann

Taxonomic studies of the Halosphaeriaceae: Corollospora Werdermann. The problems in the classification of the genus Corollospora Halosphaeriaceae, Ascomycotina; are outlined. In Corollospora nine species have been described, five are retained in Corollospora (C. maritima, C. intermedia, C. lacera, C. pulchella, C. luteola ); one species is referred to Arenariomyces (A. trifurcatus ); and two new genera are described to accommodate the remaining species. Arenariomyces trifurcatus is lectotypified and a neotype has been deposited. Key to these taxa are given.     

The preoral cavity of lower Hymenoptera (Insecta): comparative morphology and phylogenetic significance

The skeletal and muscular morphology of the preoral cavity, including the labrum, hypopharynx and labium, was examined in the imago in representatives of all the ‘symphytan’ families as well as the apocritan families Stephanidae, Megalyridae and Trigonalyidae. Xyelidae have complex modifications for masticating pollen, remarkably similiar to those of primitive Lepidoptera. These modifications, collectively termed the triturating basket complex, include an asymmetrical distal epipharyngeal wall with a microtrichial brush and an enlarged infrabuccal pouch with heavy cuticular armature that interacts with the mandibles during feeding. There were striking structural differences between the two subfamilies of Xyelidae in the ligular region; the reduced glossa and clubshaped paraglossae of Macroxyelinae resembles those of primitive Lepidoptera, while the well developed, flattened glossa and paraglossae in Xyelidae are similiar to those of most other ‘Symphyta’. A putative transformation series, leading from a relatively large labrum with unsclerotised distal epipharyngeal wall lying anterior to the mandibles, as seen in Xyelidae and enthredinoidea, to a small and heavily sclerotised labrum and distal epipharyngeal wall lying posterior to the mandibles, as seen in ‘Siricoidea’, Orussidae and the Apocrita, was revealed. These modifications may be adaptations to enable the adult of the families pupating in wood to emerge from the pupal chamber. The Anaxyelidae, Orussidae and Apocrita have similiar configurations of the glossa and nsertions of the ventral premental adductors. This indicates a close affinity of the Anaxyelidae to Orussidae + Apocrita, a hypothesis that is in conflict with other character systems. The Orussidae and Stephanidae share a unique condition in the development of a pair of large apodemes attached to the labrum; this renders the groundplan state of the labrum in the Apocrita uncertain. Twentyfive characters were defined in an attempt to eludicate the ‘Symphyta’–Apocrita transition. A numerical cladistic analysis of the characters was undertaken, resulting in 522 minimum length trees. The characters are also discussed with reference to a cladogram which resulted from an analysis of the characters derived from the present study and a survey of characters from literature.     

Giant sawflies and their kin: morphological phylogeny of Cimbicidae (Hymenoptera)

The Cimbicidae is a small family including the largest extant true sawflies (Tenthredinoidea). It comprises four subfamilies, three of which have a northern hemisphere distribution (Abiinae, Cimbicinae – Holarctic/Oriental; Corynidinae – Palaearctic), whereas the Pachylostictinae are restricted to South America. No previous attempts have been made to evaluate the subfamily classification in a cladistic context. In the present paper, 144 morphological characters from the adult anatomy for a total of 95 species of Cimbicidae and 26 outgroup taxa are scored. All subfamilies and all genera of Cimbicidae except one are represented; all families of Tenthredinoidea are represented in the outgroup. Equal weights (EW) and implied weights (IW) analyses are conducted in tnt . The results largely corroborate the existing subfamily classification, except for Pachylostictinae which are paraphyletic in IW analyses with low K‐values. Abiinae + Cimbicinae is always retrieved and strongly supported; Corynidinae + Pachylostictinae is retrieved in most analyses but weakly supported. Revised diagnoses of the subfamilies are provided. Several genera are retrieved as monophyletic, notable exceptions being Praia and Trichiosoma, which are polyphyletic. The evolution of large body size in Cimbicidae is briefly discussed; possible related phenomena are intrasexual competition and mimicry, i.e. resemblance to large apids or vespids.