The morphology of the larval head of Tipulidae (Diptera, Insecta) - The dipteran groundplan and evolutionary trends

External and internal head structures of the larva of Tipula montium are described in detail. The results are compared to conditions found in other representatives of Tipuloidea and other dipteran and antliophoran lineages. Despite of the conceivably basal position of Tipulomorpha within Diptera, the larvae are mainly characterised by derived features. The partially retracted head, the specific hemicephalic condition and several other derived character states support the monophyly of Tipuloidea. A clade comprising Tipuloidea excluding Pediciidae is suggested by the strongly retracted head, by deep dorsolateral incisions of the head capsule, by a distinctly toothed anterior premental margin, by the loss of the second extrinsic maxillary muscle, and possibly by the loss of the pharyngeal filter. Eriopterinae and Hexatominae are characterised by a tendency towards an extreme reduction of the head capsule. Limoniinae, Cylindrotomidae, and Tipulidae form a clade supported by the presence of a premaxillary suture. This implies the non-monophyly of Limoniidae. A feature shared by Cylindrotomidae and Tipulidae is the presence of a movable lacinia mobilis. However, this is arguably a plesiomorphic feature, as it also occurs in Nannochoristidae. Features of the larval head of Trichoceridae, which were included in Tipulomorpha, do not show affinities with those of Tipuloidea. Trichocerid larvae share a specialised subdivided mandible with larvae of psychodomorph groups. Tipuloidea are a highly specialised group. The characters examined did not reveal plesiomorphic features supporting a basal position, and features suggesting closer affinities with Brachycera are vague. The evolution of dipteran larval head structures was apparently strongly affected by the loss of legs and the tendency to live in cryptic habitats. Diptera are the group of Endopterygota with the highest number of apomorphic features of the larval head. The appendages are generally simplified and the muscular apparatus is strongly reduced. Specialised features evolving within dipteran lineages include specifically arranged brushes of hairs on the labrum and epipharynx, movable messores, subdivided mandibles, different mandibular brushes, and a far-reaching reduction of labial parts.     

The complete mitochondrial genome of Nephrotoma scalaris parvinotata (Brunetti 1918) (Diptera: Tipulidae) and insights into the phylogeny of Tipulomorpha

Craneflies (Tipuloidea or Tipulidae sensu lato) are one of the most diverse groups of true flies (Insecta, Diptera). The Tipuloidea and perhaps the Trichoceridae formed the infraorder Tipulomorpha, which is traditionally considered the most basal group of Diptera. Relationships among Tipulomorpha and the phylogenetic position of this infraorder within the whole Diptera remain to be settled. A mitochondrial genome (mitogenome) phylogeny of Diptera was produced to test the relationships within Tipulomorpha and its phylogenetic position. A complete mitogenome of Nephrotoma scalaris parvinotata (Tipuloidea, Tipulidae) was firstly sequenced with a next-generation sequencing approach. Compared with the published mitogenomes of Tipuloidea, the new mitogenome had a larger genome size (17,862 nt), due to a longer non-coding control region. The gene order was identical to Drosophila yakuba. Phylogenetic reconstructions using different inference methods recovered Tipulomorpha as monophyletic. And the Tipulomorpha was retrieved in a relatively basal position in Diptera. Within Tipulomorpha, the Tipuloidea and the Trichoceridae were strongly supported as reciprocally monophyletic. Relationships within Tipuloidea were resolved as (Pedicidae + (Limoniidae + (Cylindrotomidae + Tipulidae))). Well supported relationships include: Pedicidae was the sister group of (Limoniidae + (Tipulidae + Cylindrotomidae)); Limoniidae was paraphyletic with respect to (Tipulidae + Cylindrotomidae); Cylindrotomidae was the sister group of Tipulidae. The newly sequenced N. scalaris parvinotata clustered with other two Nephrotoma species at a derived position in Tipuloidea.     

The adult head morphology of the hessian fly Mayetiola destructor (diptera,cecidomyiidae)

The adult head of the Hessian fly Mayetiola destructor was examined and described in detail. Morphological features are evaluated with respect to phylogenetic implications and possible effects of miniaturisation. Preserved groundplan features of Diptera are the orthognathous orientation of the head, the vestiture of small microtrichia (possible autapomorphy), filiform antennae inserted frontally between the compound eyes, the presence of a clypeolabral muscle (possible autapomorphy), the presence of labellae (autapomorphy), and the presence of only one premental retractor. Potential synapomorphies of the groups assigned to Bibionomorpha are the origin of M. tentorioscapalis medialis on the frons and the loss of M. craniolacinialis. Further apomorphies of Cecidomyiidae identified in Mayetiola are the unusually massive anterior tentorial arm, the absence of the labro‐epipharyngeal food channel, the absence of the lacinia, and the presence of antennal sensilla connected by a seta, a feature not known from any other group of Diptera. The very large size of the compound eyes (in relation to the entire head surface) and the complete loss of ocelli are possible effects of miniaturization. The large size of the brain (in relation to the cephalic lumen), the unusual shape of the optic lobes, and the absence of the frontal ganglion as a separate structure are probably also linked with size reduction. J. Morphol. 274:1299–1311, 2013. © 2013 Wiley Periodicals, Inc.     

First μ‐CT‐based 3D reconstruction of a dipteran larva—the head morphology of protanyderus (tanyderidae) and its phylogenetic implications

The larval head of Protanyderus was examined and documented using innovative techniques, with emphasis on internal structures. A chart listing all head muscles of dipteran larvae and other holometabolan groups is presented in the Supporting Information. The results are compared to conditions found in other nematoceran lineages. The larval head of Protanyderus is characterized mainly by plesiomorphic character states such as the complete and largely exposed head capsule, the long coronal suture, V‐shaped frontal sutures, lateral antennal insertion areas, a transverse labrum, a nearly horizontal plane of mandibular movements, mandibles lacking a movable distal part, a mesal hook and mesal or distal combs, separated maxillary endite lobes, a comparatively complete array of muscles, and a brain only partly located within the head capsule. An anteriorly toothed hypostomal plate and dense labral brushes of microtrichiae are also likely groundplan features of Diptera. The pharyngeal filter is a possible apomorphy of Diptera excl. Deuterophlebiidae (or Deuterophlebiidae + Nymphomyiidae). The messors have also likely evolved early in the dipteran crown group but are absent in the groundplan. The phylogenetic interpretation of externolateral plates with growth lines is ambiguous. Autapomorphies of Tanyderidae are differences between the third and fourth instar larvae, the roof‐like extension above the antennal insertion area, the dorsal endocarina, and the posterodorsal internal ridge. The phylogenetic position of Tanyderidae is controversial, but features of the larval head do not support a proposed sistergroup relationship between Tanyderidae and Psychodidae. Both groups differ in many features of the larval head, and we did not identify a single potential synapomorphy. Larval characters alone are insufficient for a reliable phylogenetic reconstruction, though they vary greatly and apparently contain phylogenetic information. The evaluation of these features in the context of robust molecular phylogenies will be a sound basis for the reconstruction of complex evolutionary scenarios for the megadiverse Diptera. Diptera. J. Morphol. 2012. © 2012 Wiley Periodicals, Inc.     

A longstanding entomological problem finally solved? Head morphology of Nannochorista (Mecoptera,Insecta) and possible phylogenetic implications

External and internal head structures of Nannochorista species were examined and described in detail. The characters are discussed with regard to their functional and phylogenetic implications. The structure of the mouthparts indicates that adults of Nannochorista feed on fluids. The loss of the mandibular muscles and the precerebral pharyngeal dilators are presumptive autapomorphies of the genus. A possible clade comprising Nannomecoptera, Siphonaptera and Diptera is supported by the presence of a labral food channel, the absence of the galea, a sheath for the paired mouthparts formed by the labium, very strongly developed labial palp muscles and cibarial dilators, and the presence of a well‐defined postcerebral pharyngeal pumping chamber. Closer affinities of Nannomecoptera with Diptera are suggested by the presence of a unique sensorial groove on the third maxillary palpomere. Further potential synapomorphies are the presence of a frontal apodeme and a primarily lamelliform mandible without teeth. The presence of a salivary channel on the laciniae and a subdivided labrum are shared derived features of Nannochorista and Siphonaptera. A derived condition present in Mecoptera including Boreidae but excluding Nannochoristidae is the secretion with a strongly developed intrinsic muscle of the salivary duct. The loss of the lateral labral retractor, the cranial muscle of the cardo, and of two of the three premental retractors, and the absence of transverse epipharyngeal muscles are potential autapomorphies of Antliophora. The formation of a maxillolabial complex is a possible synapomorphy of Hymenoptera and Mecopterida.     

Substructure of the axoneme of pterygote insect spermatozoa: Phylogenetic considerations

Spermatozoa from a great number of insect species were fixed in a tannic acid-containing fixative and the ultrastructure of the flagellar axoneme was examined in a search for apomorphies. Most of the examined species, representing a majority of insect orders. have accessory tubules outside the axoneme (hence a 9 + 9 + 2 pattern), and these consist of 16 protofilaments. Some important apomorphies concern the number of protofilaments in the accessory tubules: 13 (plus 7 inner elements) in Ephemeroptera, 13 in the (elliptic) tubules of Psocoptera + Anoplura + Mallophaga (thus a synapomorphy), 13 in Tipulidae + Brachycera, 15 in the dipteran families Dixidae + Chironomidae (with a 9 + 9 + 2 axoneme) and Culicidae + Bibionidae (with a 9 + 9 + “1” axoneme), 17 in Phasmatodea, and 17–20 in Trichoptera. Other apomorphies concern the appearance of the so-called intertubular material outside the microtubular doublets, the appearance of the interior of the various microtubules, and the loss, in some taxa, of outer or inner dynein arms of both dynein arms. In some cases, the flagellum is completely abnormal; the sperm tail of Thysanoptera, for example, consists of 27 elements of 3 different kinds. The different taxa within orders Diptera and Trichoptera have sperm tail axonemes of different appearances, where those from other orders have a rather uniform appearance. The conclusions that can be drawn from this spermatological study, generally agree with data from classical studies, except with some variations, in some cases.     

The head morphology of Clambidae and its implications for the phylogeny of Scirtoidea (Coleoptera: Polyphaga)

External and internal structures of the head of adults of Clambus are described and illustrated in detail. The results are compared with structural features found in the clambid genus Calyptomerus, in representatives of other scirtoid families, and also in species of other coleopteran suborders, notably Myxophaga. The results tentatively support the monophyly of Scirtoidea and a close relationship between Clambidae and Eucinetidae is suggested by one shared derived feature of the mandible, a long and slender apical tooth with a serrate edge. The monophyly of Clambidae is very strongly supported and Acalyptomerus is probably the sistergroup of a clade Calyptomerus + Clambinae. Potential scirtoid autapomorphies are the loss of the dorsal tentorial arms, a bulging gula, a strongly transverse labrum, and a ridge separating the mediostipes from the lacinia. However, all these features are homoplasious. The monophyly of Clambidae is supported by modifications of the head capsule which is strongly flattened and broadened, by a deep clypeofrontal incision enabling vertical antennal movements, and a series of antennal features. Synapomorphies of Clambinae + Calyptomerus (Clambidae excluding Acalyptomerus) are the conglobate body form with the ventral side of the head capsule in contact with the mesocoxae, and compound eyes integrated in the contour of the head. The completely subdivided eye is an autapomorphy of Clambus. An entire series of features is shared by Clambidae (or Scirtoidea) and Myxophaga. Most of them are apomorphies that apparently evolved independently in both groups. However, the presence of well‐developed maxillary and labial glands is arguably a retained groundplan feature of Coleoptera, with parallel loss in Archostemata, Adephaga and various groups of Polyphaga. J. Morphol. 277:615–633, 2016. © 2016 Wiley Periodicals, Inc.     

Phylogenetic synthesis of morphological and molecular data reveals new insights into the higher‐level classification of Tipuloidea (Diptera)

Tipuloidea, the crane flies, are a diverse lineage of true flies (Insecta: Diptera) whose phylogenetic classification and taxonomy remain a challenge. Here we present the results of a quantitative phylogenetic analysis of Tipuloidea based on combined morphological characters (adult, larvae and pupae) and nuclear gene sequence data (28S rDNA and CAD). Forty‐five species, from 44 genera and subgenera, were sampled, representing the four putative families of Tipuloidea (Cylindrotomidae, Limoniidae, Pediciidae and Tipulidae sensu stricto). Analyses of individual datasets, although differing in overall topology, support the monophyly of several major lineages within Tipuloidea. Parsimony and Bayesian analyses using individual morphological and molecular datasets resulted in incongruent topologies. Increased resolution and tree support was obtained when both datasets (morphology and genes) were combined, in both combined evidence parsimony and Bayesian analyses, than when analysed separately. The recovered consensus phylogeny was not consistent with any previously proposed Tipuloidea classification, with previous importance assigned to character states shown here to represent losses and reversals seen as a major factor influencing erroneous classification. The results provided here, together with evidence from previous analyses, were used to append the Tipuloidea classification to supported evolutionary lineages. Tipuloidea is presented as two families: Pediciidae and Tipulidae. Pediciidae is recovered as the sister group to all remaining Tipuloidea. Our current phylogenetic hypothesis is not consistent with the existing subfamilial classification of the ‘Limoniidae’, which is paraphyletic with respect to a well‐supported Tipulinae + Cylindrotominae clade, whereas the three ‘limoniid’ subfamilies are para‐ or polyphyletic. The recognition of ‘Limoniidae’ as a valid monophyletic family is discouraged and the subfamilies of ‘Limoniidae’ are amended and placed within Tipulidae. A revised phylogenetic classification is proposed for the crane flies based on a synthesis of evidence from multiple genes and morphology.     

Global diversity of craneflies (Insecta,Diptera: Tipulidea or Tipulidae <Emphasis Type="Italic">sensu lato</Emphasis>) in freshwater

The Tipulidae s.l.—craneflies—are one of the largest groups of the Diptera containing over 15,270 valid species and subspecies. The immatures of the majority of species live in aquatic or semiaquatic habitats. Some aquatic species live entirely submerged and lack functional spiracles, others come to the surface to take oxygen by using spiracles positioned at the end of the abdomen. Semiaquatic species occur in a wide range of habitats. The semiterrestrial and terrestrial larvae live in environments that are moist or at least humous. All adult craneflies are terrestrial. Conflicting hypotheses on the phylogenetic position of the Tipuloidea within the Diptera continue to exist: some authors consider them to represent one of the oldest lineages of the Diptera, others suppose a close relationship to the Brachycera, the true flies. Current systematic knowledge of the Tipuloidea indicates that the Palaearctic region contains the highest number of genus-group taxa, while the Neotropical region has the highest number of species and subspecies. The Afrotropical and Australasian regions are relatively poor respectively in genera and subgenera and in species and subspecies. The oldest fossils that represent the Tipuloidea date back to the Lower Triassic at about 240 million years. Present-day general distribution patterns of many higher taxa of Tipuloidea probably have a Pangean or Gondwanan origin. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. Guest editors: E. V. Balian, C. Lévêque, H. Segers & K. Martens Freshwater Animal Diversity Assessment.     

Resolving insect phylogeny: The significance of cephalic structures of the Nannomecoptera in understanding endopterygote relationships

The Nannomecoptera are among the most enigmatic and controversial taxa of endopterygote insects, the phylogenetic resolution of which is crucial to understanding the evolution of neopteran insects. Once considered a subordinate lineage within the Mecoptera, renewed interest in nannochoristids has been prompted by evidence that the Nannomecoptera are not admissible to the clade of extant scorpion flies but are more likely to belong to the clade Siphonaptera + Nannomecoptera + Diptera. The overarching purpose of the present account is to provide novel and extensive morphological character traits in addition to those already existing for adult structures. The aim is to determine if these traits support molecular data sets that have been suggested elsewhere to clarify the phyletic position of Nannochoristidae. This account focuses on nannomecopteran larvae, which unlike those of other mecopterans have received little attention. Thus, the thrust of this investigation is to provide detailed anatomical data on nannochoristid larvae for a targeted inquiry into their phylogenetic affinities. The described characters are discussed and presented in a data matrix comprising representatives of all endopterygote orders. While the study is based primarily on the New Zealand species Nannochorista philpotti, it is proposed that all nannomecopteran larvae will prove to be similar to this taxon in most if not all structural features of significance to a higher-level phylogenetic context.     

On the head morphology of Phyllium and the phylogenetic relationships of Phasmatodea (Insecta)

Friedemann K., Wipfler B., Bradler S. and Beutel R.G. 2011 . On the head morphology of Phyllium and the phylogenetic relationships of Phasmatodea (Insecta). —Acta Zoologica (Stockholm) 00 : 1–16. External and internal head structures of Phyllium siccifolium are described in detail. The findings are compared with conditions found in other phasmatodeans and members of other neopteran lineages. The compiled 125 characters were analysed cladistically. A clade Eukinolabia (Phasmatodea + Embioptera) was confirmed. Synapomorphies of these two taxa are the shift of the origin of M. tentorioparaglossalis to the hind margin of the prementum, the presence of M. tentorioscapalis medialis, and antennal muscles that originate exclusively on the anterior tentorial arms. Within Eukinolabia, the position of Timema remains somewhat ambiguous because of missing anatomical data. However, it was confirmed as sister group of Euphasmatodea in a monophyletic Phasmatodea. Apomorphic groundplan features of Euphasmatodea are salivary ducts with separate external openings, apically rounded glossae, the presence of the galealobulus, and the reduction of the antennifer. The monophyly of Neophasmatidae was confirmed. Autapomorphies are the loss of M. frontobuccalis posterior, the anteriorly or dorsally directed maxillary palps, and the reduction of the mandibular incisivi. The analysis of characters of the head yielded three new autapomorphies of Phylliinae, the presence of a protuberance on the attachment site of the dorsal tentorial arms, dorsoventrally flattened maxillary‐ and labial palps, and possibly the narrow and U‐shaped field of trichomes on the apical part of the galea.     

Cephalic morphology of Hymenopus coronatus (Insecta: Mantodea) and its phylogenetic implications

External and internal head structures of the mantodean Hymenopus coronatus are examined and described in detail. The results are elaborately compared with the literature. Strong crests on the anterior tentorial arms that articulate with the subantennal suture, a parietal suture and glossae and paraglossae with anteriorly bent tips are proposed as new potential apomorphies for Mantodea while a head capsule being wider than long, enlarged compound eyes, the presence of a frontal shield or scutellum, lateral lobes in the anterior tentorial arms, the presence of a transverse and an interantennal suture and the reduction of the mentum are confirmed as apomorphies, As potential apomorphies for Dictyoptera the reduction of Musculus tentoriobuccalis lateralis (M. 49) is newly presented and a “perforate” tentorium, lacinial incisivi that are located in a galeal pouch and the presence of a postmola are confirmed. The present study shows the value of cephalic morphology for phylogenetic analysis but also points out that further studies including evolutionary key taxa are essential for resolving the evolutionary adaptations among dictyopterans.     

Expression of <Emphasis Type="Italic">defective proventriculus</Emphasis> during head capsule development is conserved in <Emphasis Type="Italic">Drosophila</Emphasis> and stalk-eyed flies (<Emphasis Type="Italic">Diopsidae</Emphasis>)

Hypercephaly, in the form of lateral extensions of the head capsule, is observed in several families of Diptera. A particularly exaggerated form is found in Diopsid stalk-eyed flies, in which both eyes and antennae are laterally displaced at the end of stalks. The processes of early development and specification of the head capsule in stalk-eyed flies are similar to those in Drosophila melanogaster. In Drosophila the homeobox gene ocelliless (oc) shows a mediolateral gradient of expression across the region of the eye-antennal imaginal disc that gives rise to the head capsule and specifies the development of different head structures. The genes and developmental mechanisms that subsequently define head shape in Drosophila and produce hypercephaly in stalk-eyed flies remain unclear. To address this, we performed an enhancer trap screen for Drosophila genes expressed in the same region as oc and identified the homeobox gene defective proventriculus (dve). In the eye-antennal imaginal disc, dve is coexpressed with oc in the region that gives rise to the head capsule and is active along the medial edge of the antennal disc and in the first antennal segment. Analyses of dve expression in mutant eye-antennal discs are consistent with it acting downstream of oc in the development of the head capsule. We confirm that orthologues of dve are present in a diverse panel of five stalk-eyed fly species and analyse patterns of dve sequence variation within the clade. Our results indicate that dve expression and sequence are both highly conserved in stalk-eyed flies.M. Carr and I. Hurley contributed equally to this work.     

Head morphology of Caurinus (Boreidae, Mecoptera) and its phylogenetic implications

External and internal head structures of Caurinus dectes were examined and described in detail. The features are compared to conditions found in other groups of Antliophora. Caurinus is obviously crucial for the reconstruction of the mecopteran and antliophoran groundplan. It displays a remarkable series of plesiomorphic character states such as a complete clypeolabral suture, the presence of M. hypopharyngomandibularis (M. 13) and M. frontohypopharyngalis (M. 41), a subdivided clypeus, a short head without rostrum, a dorsal tentorial arm attached to the head capsule, the absence of a cranial dilator of the antenna, and large mandibles with a well developed apical tooth, two distinct subapical teeth, and a basal molar part. The first three plesiomorphic features render potential autapomorphies of Mecoptera in the traditional sense invalid. Autapomorphies of Caurinus are the distinctly flattened labrum, the absence of the labroepipharyngeal muscle, the very large size of M. 13, the strongly enlarged penultimate palpomeres, the partition of M. 41, the very strongly developed precerebral sucking chamber, strongly curved optic lobes, the presence of a large protocerebral extension in the genal region and deep posterior excavations of the protocerebrum. The maxillolabial plate, the absence of cardines as separate structures, the reduction of ocelli, and the origin of maxillary palp muscles on a median ridge or area of the maxillolabial plate are likely autapomorphies of Boreidae. Another potential autapomorphy of the family is the presence of longitudinal furrows on the mandibles. However, they are absent in Boreus. The thick strongly sclerotised, median ridge of the maxillolabial plate, the missing retractibility of the prementum, the absence of extrinsic labial muscles, and the presence of a median ridge on the prepharyngeal roof suggest a clade Boreus + Hesperoboreus. The origin of extrinsic maxillary muscles from the clypeus has probably evolved independently in Boreus and Hesperoboreus, and in Panorpa, respectively. The absence of M. craniolacinialis and the presence of a row of several subapical mandibular teeth are autapomorphies of Boreus. The presence of a specific intrinsic muscle of the salivary duct and a membranous galea enclosing the labrum and mandibular base are derived features shared by Boreidae and Pistillifera (galea absent in Nannochorista, Siphonaptera and Diptera). The loss of M. frontolabralis (M. 8) is a potential apomorphy of Mecoptera incl. Siphonaptera. A sister group relationship between Boreidae and Siphonaptera is not supported by characters of the adult head. Head structures of Siphonaptera are extremely modified in correlation with ectoparasitic habits.     

The dipteran sperm tail: ultrastructural characteristics and phylogenetic considerations

The sperm tail from representatives of several families of Diptera has been examined by high resolution electron microscopy and a computer analysis that improved the visualization of recorded patterns. A considerable variability in sperm tail structure is found within Diptera, and is actually greater than that of any other insect order. The 'generalized insect sperm axoneme'. which is characterized as a 9+9+2 axoneme and by the accessory microtubules having 16 protofilaments, was found only in some dipterans; these are members of Mycetophilidae. From this fact we conclude that Mycetophilidae is likely to be the most primitive extant dipteran group. Another mycetophilid, Boletina , was seen to have accessory tubules with 15 protofilaments as have members of families Dixidae, Chironomidae, Culicidae, and Bibionidae. The last two families have spermatozoa of a type designated as 9+9+'1' there is a central rod rather than two microtubules. We regard this 9+9+'1'pattern with 15 protofilaments to represent a synapomorphic feature. Representatives of the neatoceran families Tipulidae and Trichoceridae have accessory tubules with 13 protofilaments as do examined members of several brachyceran families. Brachycera is hence likely to be derived from the vicinity of the tipulid family. The intertubular material is small in Mycetophilidae and most nematoceran groups, whereas in Tipulidae and Brachycera it is enlarged; here it bridges the space between the accessory tubules and contains various inclusions.     

The larval head of Exechia (Mycetophilidae) and Bibio (Bibionidae) (Diptera)

Exechia and Bibio have retained several plesiomorphic groundplan features of Diptera and Bibionomorpha, including a fully exposed and sclerotized head capsule, the transverse undivided labrum, the absence of movable premandibles, and undivided mandibles without combs. The fusion of the hypostomal bridge with the head capsule and largely reduced antennae are derived features shared by both taxa. The absence of teeth at the anterior hypostomal margin is a potential autapomorphy of Bibionomorpha. A basal position of Anisopodidae is suggested by a number of plesiomorphies retained in this family. Apomorphies of Bibionomorpha excluding Anisopodidae are the reduction of tentorial elements, the partial fusion of the labrum and clypeus, one-segmented antennae, the absence of a separate submental sclerite, the loss of the labial palpus, and the reduction of the pharyngeal filter apparatus. Head structures of Bibio are largely unmodified. The subprognathous orientation is one of few autapomorphic features. In contrast, the mouthparts of Exechia are highly modified in correlation with the specialized food uptake. The rasping counterrotating movements of maxillae and mandibles with teeth oriented in opposite directions are carried out by strongly developed extensors and flexors of the paired mouthparts. The modified labium mechanically supports the “drill head” formed by the mandibles und maxillae. The necessary stability of the head capsule is provided by the hypostomal bridge which also compensates the far-reaching reduction of the tentorium.     

The implications of function on the origin and homologies of the dipterous wing

Abstract The origin of Diptera, and the homologies of the dipteran wing, are re-examined in the light of recent studies on the flight biomechanics and functional wing morphology of Diptera and of Panorpa. Significant Diptera apomorphies are identified, relevant fossils discussed, and a hypothetical wing ground-plan figured.
The arculus, the modified clavus and the anteroposterior asymmetry of the fly wing seem to be adaptations to a mode of flight in which instantaneous wing pitch and camber are controlled automatically, rather than by muscular action; probably in association with the development of asynchronous power musculature.
Tillyard's Cu2 (=CUP) is believed to be a secondary pseudo-vein, his 1A to be the true CuP and 2A to be 1A.
The late Permian fossil Permotipula Patricia is almost certainly a member of the Diptera stem-group, possibly even of the crown-group. The Mesozoic Laurentipteridae and the Permian Permotanyderidae are other possible, but not certain, stem-group members.     

The larval head structures of Podagricomela shirahatai (Chûjô) (Chrysomelidae,Galerucinae, Alticini) and morphological effects of leaf mining

Head structures of the leaf mining larva of the chrysomelid species Podagricomela shirahatai are described and illustrated. Internal and external structures were reconstructed three dimensionally based on image stacks obtained with microcomputed tomography. The larval head is characterized by prognathism, a dorsoventrally compressed shape, a flattened maxillolabial complex, a completely reduced coronal suture, and the presence of a deep, V‐shaped posterior emargination of the head capsule. Internal structures are not distinctly affected by leaf mining. The cephalic features are compared with conditions found in surface feeding and root feeding alticine larvae and also with characters of chrysomeline larvae of Chrysomela populi Linnaeus. Possible correlations between modifications of the larval head and different feeding behaviors are discussed. Characters are also discussed with respect to possible phylogenetic implications. Some derived features are apparently due to phylogenetic constraints. Apomorphies characterizing alticine larvae with distinctly different life habits are the loss of M. frontoepharyngalis (M. 9), the origin of M. tentoriostipitalis (M. 18) from the head capsule, two insertions of M. tentoriopraementalis inferior (M. 29) and the reduction of stemmata. The study underlines that the anatomical study of chrysomeloid larvae is not only highly desirable in a phylogenetic context, but also crucial for understanding the evolution of different life strategies in this extremely successful group of Coleoptera. J. Morphol. 276:446–457, 2015. © 2014 Wiley Periodicals, Inc.     

The biodiversity of Diptera in Old World rain forest surveys: a comparative faunistic analysis

Aim Identify the taxonomic patterns and the relative importance of particular families of Diptera sampled in comparative biodiversity surveys carried out at seven rain forest locations. We test and quantify the contention that different trapping methods routinely target different families. We identify the south–north (and upland/lowland) patterns and generate a set of hypotheses concerning mechanisms underlying these patterns. Location Australia and Papua New Guinea. Methods A total of 28,647 Diptera collected using canopy knockdown, yellow pan (water) traps and Malaise traps have been sorted to 56 families following these surveys. Comparative analyses across sites from Lamington National Park in south‐east Queensland, Australia to the Kau Wildlife area in Madang Province, Papua New Guinea, of the dipteran assemblages, and separately, of the 14 families which collectively made up 95.8% of the sample, are presented. Results Ordination by multi‐dimensional scaling and analyses of variances showed that the three methods complemented each other in terms of target families and, together, sampled a large proportion of the expected fauna of these sites. Ordinations on a method‐by‐method basis permitted the identification of groups of sites and analyses of variance indicated which taxa differed significantly across these groups. Main conclusions Recurrent patterns and associated hypotheses about their generation emerge from the data. These mirror floristic differences and reflect the biogeographic history of the sites since the Miocene. Clear linkages between the lowland faunas of Papua New Guinea and northern Australia are evident and are reflected in the abundances of the Dolichopodidae, Empididae, Muscidae and Tipulidae (other groupings underlined the essential difference of the New Guinean fauna which had characteristic proportions of Cecidomyiidae, Chironomidae, Dolichopodidae, Phoridae and Psychodidae). A subtropical grouping of families was evident comprising, inter alia, Chloropidae, Mycetophilidae, Drosophilidae and Phoridae which was frequently linked with the higher elevation tropical fauna at Robson's Creek, Atherton Tablelands. The long isolated, high elevation, rain‐forested massif at Eungella, central Queensland often emerged as a unique entity in the analyses, characterized by the high numbers of and proportions of Chironomidae, Psychodidae, Tipulidae and Empididae. This study supports the case for the wider use of Diptera in biodiversity analyses, complementing extensive earlier analyses which have used, predominantly, large coleopteran assemblages. The results indicate the potential power of family‐level analyses at large geographical scales and contribute to the ongoing debate on ‘taxonomic sufficiency’.