Vibrational Communication in Two Sympatric Species of Mantophasmatodea (Heelwalkers)

The communication via percussion of the abdomen on the substrate for species recognition and mate location of males and females of two sympatric species of the recently described insect order Mantophasmatodea (Heelwalkers) was investigated. Each sex produced a single and distinctive call. The female call consisted of repeated single pulses, whereas the more complex male call comprised repeated pulse trains. The calls of males and females of the two species were of similar general structure, but differed in most temporal characters such as pulse and pulse train repetition time. In behavioral playback experiments females reacted to the call of conspecific males by calling and decreasing locomotion. When stimulated with the call of the heterospecific, sympatric male, females showed no reaction. Males exhibited abdominal rubbing, high tapping rates, increased activity (both movement and active searching) as well as characteristic searching behavior at branch nodes, when presented with the conspecific female call. Being stimulated with the playback of the heterospecific female call and the conspecific male call respectively, males responded with less intense locomotor and searching behavior. The drumming behavior in the control situation (no playback) suggests that males sometimes call in the absence of other individuals.     

Surface structures of the antenna of Mantophasmatodea (Insecta)

The cuticular fine structure of the antenna in Mantophasmatodea (Austrophasmatidae: Hemilobophasma montaguense, Austrophasma gansbaaiense) is described based on SEM images. The armature of sensilla (=s.) on the basiflagellum (14 basal flagellomeres, the distal ones of which are subdivided) and distiflagellum (7 distal flagellomeres) differs strongly. A basiflagellomere has a sporadic vestiture of prominent s. chaetica B as well as distal s. scolopidia and scattered s. coeloconica. The distiflagellum also bears scattered s. chaetica B and s. coeloconica but is also densely covered with sensilla of various other types: numerous s. trichodea and s. basiconica, sporadic s. coelocapitula, and a probably new type of branched sensilla; the distiflagellum is probably the main sensory region, including gustatory and olfactory chemoreception, mechanoreception, and hygroreception. The scape and pedicel also bear s. chaetica B, and s. chaetica A arranged in 4 (scape) or 2 (pedicel) hair-plates. Terminal s. campaniformia are only found on the pedicel. A ‘dark spot’ is present apically on distiflagellomeres 6 (as reported previously) and 1. The two spots are of similar structure and are possibly associated with glands; each comprises a complicated external aperture and a larger internal pouch enclosing a cavity; projections protrude from the pouch walls into the cavity. The surface structure of the basiflagellomeres shows differences that are possibly species specific. An overview is given on antennal apomorphies in Mantophasmatodea.     

Phylogeny of the major lineages of Membracoidea (Insecta: Hemiptera: Cicadomorpha) based on 28S rDNA sequences

Analysis of sequences from a 3.5-kb region of the nuclear ribosomal 28S DNA gene spanning divergent domains D2-D10 supports the hypothesis, based on fossil, biogeographic, and behavioral evidence, that treehoppers (Aetalionidae and Membracidae) are derived from leafhoppers (Cicadellidae). Maximum-parsimony analysis indicated that treehoppers are the sister group of a lineage comprising the currently recognized cicadellid subfamilies Agalliinae, Megophthalminae, Adelungiinae, and Ulopinae. Based on this phylogenetic estimate, the derivation of treehoppers approximately coincided with shifts in physiology and behavior, including loss of brochosome production and a reversal from active, jumping nymphs to sessile, nonjumping nymphs. Myerslopiidae, traditionally placed as a tribe of the cicadellid subfamily Ulopinae, represented a basal lineage distinct from other extant membracoids. The analysis recovered a large leafhopper lineage comprising a polyphyletic Deltocephalinae (sensu stricto) and its apparent derivatives Koebeliinae, Eupelicinae (polyphyletic), Selenocephalinae, and Penthimiinae. Clades comprising Macropsinae, Neocoelidiinae, Scarinae, Iassinae, Coelidiinae, Eurymelinae + Idiocerinae, Evacanthini + Pagaroniini, Aphrodinae + Ledrinae (in part), Stenocotini + Tartessinae, and Cicadellini + Proconiini were also recovered with moderate to high branch support. Cicadellinae (sensu lato), Ledrinae, Typhlocybinae, and Xestocephalinae were consistently polyphyletic on the most-parsimonious topologies, but constraining these groups to be monophyletic did not significantly increase the length of the cladograms. Relationships among the major lineages received low branch support, suggesting that more data are needed to provide a robust phylogenetic estimate.     

Phylogeny of the mayfly family Leptohyphidae (Insecta: Ephemeroptera) in South America

Abstract.  A cladistic analysis of the South American members of the Ephemeropteran family Leptohyphidae is presented. A matrix of 73 taxa and 124 morphological characters was analysed under two distinct weighting criteria (implied weighting, which weights characters as a whole, and self-weighted optimization, which differentially weights character state transformations). To assess the monophyly of the Leptohyphidae, representatives of Ephemerellidae, Ephemerythidae, Machadorythidae, Teloganodidae, Tricorythidae, Coryphoridae and Melanemerellidae were also included. Trees were rooted in Ephemerellidae. Conspicuous differences in consensus topology occur when transformation costs among character states are weighted (including asymmetries). The differences in the assessments of character reliability in the two weighting criteria used are discussed. In many cases, self-weighting, in allowing for asymmetries in transformation costs, considered many of the character state transformations as more reliable (= informative) than implied weights (which needlessly down-weighted the whole character). The results confirm the monophyly of Leptohyphidae and support its sister-group relationship with Coryphoridae. The shortest trees do not support the recently proposed division of Leptohyphidae into two subfamilies. Ephemerelloidea higher classification is discussed briefly.     

Phylogeny of Polycladida (Platyhelminthes) based on mtDNA data

A phylogenetic analysis of Polycladida based on two partial mitochondrial genes (cox1 and 16S) is provided. The analysis includes 30 polyclad terminals that represent species from the two taxa which traditionally divide the groups Cotylea and Acotylea. Our phylogenetic analyses produced a well-supported hypothesis that confirms the monophyly of Polycladida, as well as Acotylea and Cotylea. Within Acotylea, there are two lineages not highly supported: on one hand, Leptoplanoidea (excluding Hoploplana elisabelloi) and one Stylochoidea member (Pseudostylochus intermedius) (classification sensu Faubel, 1983, 1984), and on the other hand, Stylochoidea members together with Discocelis tigrina and H. elisabelloi. The genera Stylochus and Imogine are not monophyletic. Within Cotylea, Pseudocerotidae and Euryleptidae are monophyletic, though not highly supported, while Prosthiostomidae is not. Euryleptoidea is paraphyletic. The genera Pseudobiceros and Pseudoceros are monophyletic and highly supported. Our results suggest that, within Acotylea, the prostatoid organs of Discocelis may have been derived from a prostatic vesicle. The genus Hoploplana could be included in Stylochoidea. Within Cotylea, the common ancestor of Euryleptidae and Pseudocerotidae might have been an aposematic animal with tentacles.     

Phylogeny of earwigs (Insecta: Dermaptera) based on molecular and morphological evidence: reconsidering the classification of Dermaptera

Abstract. Dermaptera (earwigs) is a cosmopolitan order of insects, the phylogenetic relationships of which are poorly understood. The phylogeny of Dermaptera was inferred from large subunit ribosomal (28S), small subunit ribosomal (18S), histone-3 (H3) nuclear DNA sequences, and forty-three morphological characters. Sequence data were collected for thirty-two earwig exemplar taxa representing eight families in two suborders: Hemimeridae (suborder Hemimerina); Pygidicranidae, Anisolabididae, Labiduridae, Apachyidae, Spongiphoridae, Chelisochidae and Forficulidae (suborder Forficulina). Eighteen taxa from ten additional orders were also included, representing Ephemeroptera, Odonata, Orthoptera, Phasmida, Embiidina, Mantodea, Isoptera, Blattaria, Grylloblattodea and Zoraptera. These data were analysed via direct optimization in poy under a range of gap and substitution values to test the sensitivity of the data to variations in parameter values. These results indicate that the epizoic Hemimerus is not sister to the remaining Dermaptera, but rather nested as sister to Forficulidae + Chelisochidae. These analyses support the paraphyly of Pygidicranidae and Spongiphoridae and the monophyly of Chelisochidae, Forficulidae, Anisolabididae and Labiduridae.     

Structure and function of the arolium of Mantophasmatodea (Insecta)

All species of the insect order Mantophasmatodea characteristically keep the 5th tarsomere and pretarsus (arolium plus two claws) turned upwards and off the substrate. The unusually large arolium was studied in two species of Mantophasmatodea using bright field light microscopy, reflection microscopy, fluorescence microscopy, TEM, SEM, and Cryo‐SEM. It contains an epithelial gland, numerous tracheoles, and nerves. The gland consists of enlarged epithelial cells with large nuclei, mitochondria, RER, golgi complexes, microtubules, and numerous secretion vesicles. Evidence for exocytosis of the vesicles into the gland reservoir between the epithelial gland and the thick cuticle could be observed. Cryo‐SEM revealed that the ventral side of the arolium and distal part of its dorsal side are covered with a liquid film. Fluid footprints of arolia of individuals walking on a glass plate also indicate the presence of secretory fluid on the arolium surface. Behavioral experiments using animals with ablated arolia showed that representatives of Mantophasmatodea do not need their arolia to detect and respond to vibratory communication signals nor to catch small to medium‐sized prey. Individuals with ablated arolia were not able to move upside down on a smooth glass plate. We conclude that Mantophasmatodea use their arolia for attachment when additional adhesion force is required (e.g. windy conditions, handling large prey, mating). They can bring their arolia in contact with the surface in a very fast reflex (18.0 ± 9.9 ms). The secretory fluid found on the surface is produced by the gland and transported to the outside, presumably through small pore channels, to enhance adhesion to the substrate. J. Morphol., 2009. © 2009 Wiley‐Liss, Inc.     

Postembryonic development of the unique antenna of Mantophasmatodea (Insecta)

The postembryonic antennal development and life cycle of a member of the insect order Mantophasmatodea (Lobatophasma redelinghuysense) was investigated using a series of annulus counts and a time sequence of head capsule measurements. The life cycle comprised six instars. Females achieved significantly larger head capsules from instar 2 onwards, resulting in adult females having a larger mean head capsule diameter (2.58 mm) than males (2.27 mm). Antennae of first instar larvae comprised a smooth four-segmented basiflagellum and a seven-segmented, sensilla-rich distiflagellum. Lengthening of the basiflagellum was achieved by the addition of two annuli per moult, generated by division of the basal annulus (meriston). Annulus number and the unique annulation pattern of the distiflagellum remained constant until adulthood. The segmentation pattern of adult antennae (comprising a basiflagellum and a distiflagellum of 14 and seven annuli respectively) and mode of antennal elongation was consistent for all 11 species examined. Subdivisions in basiflagellar annuli were observed in adults of all species examined, although they are not considered to be true annular divisions. The structure of the mantophasmatodean antenna appears to be autapomorphic within Insecta, bearing little resemblance to that of Grylloblattodea, Dictyoptera or Phasmatodea, all putative sister groups of the Mantophasmatodea. However, the mode of flagellar elongation most closely resembles that of Isoptera, Blattaria and Dermaptera.     

Phylogeny of South African Gnaphalieae (Asteraceae) based on two noncoding chloroplast sequences

The Gnaphalieae are a group of sunflowers that have their greatest diversity in South America, Southern Africa, and Australia. The objective of this study was to reconstruct a phylogeny of the South African Gnaphalieae using sequence data from two noncoding chloroplast DNA sequences, the trnL intron and trnL/trnF intergenic spacer. Included in this investigation are the genera of the Gnaphalieae from the African basal groups, members of the subtribes Cassiniinae, Gnaphaliinae, and Relhaniinae, and African representatives from the large Old World genus Helichrysum. Results indicate that two Gnaphaloid genera, Printzia and Callilepis, should be excluded from the Gnaphalieae. In most trees the Relhaniinae s.s. (sensu stricto) and some of the basal taxa comprise a clade that is sister to the remainder of the tribe Gnaphalieae. The Relhaniinae, which are restricted to Africa, are not a monophyletic group as presently circumscribed, nor are the South African members of Helichrysum, the Cassiniinae and Gnaphaliinae. There is general agreement between our molecular analysis and that of morphology, particularly in the terminal branches of the trees.     

Phylogeny of caddisflies (Insecta, Trichoptera)

Trichoptera are holometabolous insects with aquatic larvae that, together with the Lepidoptera, comprise the Amphiesmenoptera. Previous phylogenetic hypotheses and progress on our ongoing data collection are summarized. Fragments of the large and small subunit nuclear ribosomal RNAs (D1, D3, V4–5), the nuclear elongation factor 1 alpha gene and a fragment of mitochondrial cytochrome oxidase 1 (COI) were sequenced, and molecular data were combined with previously published morphological data. Equally and differentially weighted parsimony analyses were conducted in order to present a phylogeny of Trichoptera, including 43 of 45 families. Our phylogeny closely resembles that proposed by Herbert Ross with respect to the relationships among suborders, with a monophyletic Annulipalpia at the base of the tree, and a clade consisting of Spicipalpia plus a monophyletic Integripalpia. The monophyly of Spicipalpia is weakly supported in the combined equally weighted analysis, and Spicipalpia is paraphyletic in the differentially weighted analysis. Within Integripalpia, our phylogeny recovered monophyletic Plenitentoria, Brevitentoria and Sericostomatoidea. Leptoceroidea was unresolved in the equally weighted analysis and monophyletic in the differentially weighted analysis. Within Annulipalpia, we recovered a basal but paraphyletic Philopotamoidea and a monophyletic Hydropsychoidea.     

Phylogeny of thrips (Insecta: Thysanoptera) based on five molecular loci

The order Thysanoptera (Paraneoptera), commonly known as thrips, displays a wide range of behaviours, and includes several pest species. The classification and suggested relationships among these insects remain morphologically based, and have never been evaluated formally with a comprehensive molecular phylogenetic analysis. We tested the monophyly of the suborders, included families and the recognized subfamilies, and investigated their relationships. Phylogenies were reconstructed based upon 5299 bp from five genetic loci: 18S ribosomal DNA, 28S ribosomal DNA, Histone 3, Tubulin‐alpha I and cytochrome oxidase c subunit I. Ninety‐nine thrips species from seven of the nine families, all six subfamilies and 70 genera were sequenced. Maximum parsimony, maximum likelihood and Bayesian analyses all strongly support a monophyletic Tubulifera and Terebrantia. The families Phlaeothripidae, Aeolothripidae, Melanthripidae and Thripidae are recovered as monophyletic. The relationship of Aeolothripidae and Merothripidae to the rest of Terebrantia is equivocal. Molecular data support previous suggestions that Aeolothripidae or Merothripidae could be a sister to the rest of Terebrantia. Four of the six subfamilies are recovered as monophyletic. The two largest subfamilies, Phlaeothripinae and Thripinae, are paraphyletic and require further study to understand their internal relationships.     

Phylogeny of the Ecnomidae (Insecta: Trichoptera)

Ecnomidae are a family of seven previously accepted extant genera having a typical Gondwanan distribution, except one genus ( Ecnomus ) being widely distributed also in the Oriental and Palearctic regions. We analysed a molecular data set of 3379 characters representing the sum of four different protein-coding genes (COI, CAD, EF-1a and POL-II). Six equally most parsimonious trees were generated from the combined data set, distributed into two distinct islands. In all maximum parsimony (MP) trees the Ecnomidae is monophyletic when the genus Zelandoptila (Psychomyiidae) is included. The sister group to Ecnomidae including Zelandoptila is Pseudoneureclipsis , previously classified in the other families. This sister-group relationship contradicts earlier findings that the Polycentropodidae are the sister group to Ecnomidae. A Bayesian analysis resulted in a monophyletic Ecnomidae when accepting inclusion of Pseudoneureclipsis , which contradicts the results from the MP analysis by leaving Zelandoptila as the sister group to Ecnomidae including Pseudoneureclipsis . In the majority rule tree from this analysis Polycentropodidae form the sister group to Ecnomidae. We were not able to obtain a monophyletic Ecnomus due to the inclusion of Psychomyillodes . We conclude that the genus Zelandoptila or Pseudoneureclipsis probably belongs to the Ecnomidae, and that Psychomyiellodes and Ecnomus are synonyms. Three additional, as yet undescribed monotypic genera from Australia and New Caledonia remain to be erected in Ecnomidae.
© The Willi Hennig Society 2009.     

Evolution and Diversity of Vibrational Signals in Mantophasmatodea (Insecta)

Vibrational communication for species identification and mate location is widespread among insects. We investigated the vibrational communication signals of 13 species of the insect order Mantophasmatodea (Heelwalkers). Males and females produce percussive signals by tapping their abdomens on the substrate to locate conspecific mates. We show that male and female calls are of similar general structure but differ in temporal characteristics. Using a principal component analysis, we demonstrate that most species can be distinguished by their calls only. Mapping the calls onto an existing molecular phylogenetic tree reveals a slow diverging drift of male call pattern but no specific trend. For females, a trend from faster towards slower pulse repetition times is indicated. Two sympatric species, Karoophasma biedouwense and Viridiphasma clanwilliamense (Austrophasmatidae), exhibit very different call parameters. The latter species produces calls rather different from all other investigated species, which might hint at reproductive character displacement.     

Gryllolattids (Insecta, Grylloblattida) from the Upper Permian of South Africa

A Late Permian fauna of grylloblattid insects (Insecta; Grylloblattida) from the KwaZulu-Natal Province (South Africa) is considered. New taxa, Liomopterites ulterior sp. nov. and L. meridionalis sp. nov. (family Liomopteridae); Normandienoptera serotina gen. et sp. nov. and Afrogrylloblattus disputabilis gen. et sp. nov. (Skaliciidae), are described. Mioloptera stuckenbergi Riek, 1973 and Mioloptoides andrei Riek, 1976 of the family Liomopteridae are redescribed.     

Phylogeny of the Neuropterida (Insecta: Holometabola)

The Neuropterida, with about 6500 known species — living fossils in a way — at the base of the Holometabola (as a sister group of the Coleoptera), comprise Raphidioptera (about 210 species, two families), Megaloptera (about 300 species, two families) and Neuroptera (6000 species, 17 families). Megaloptera + Neuroptera is argued vs. the traditional Raphidioptera + Megaloptera. Raphidioptera are undisputedly monophyletic. Monophyly of Megaloptera is the operational hypothesis, although occasionally questioned. Sucking tubes of the larvae are the most spectacular autapomorphy of Neuroptera. The construction of larval head capsules indicates three evolutionary lines: Nevrorthiformia, and Myrmeleontiformia + Hemerobiiformia. Traditional Myrmeleontiformia is Psychopsidae + (Nemopteridae + (Nymphidae + (Myrmeleontidae + Ascalaphidae))), the present approach is (Psychopsidae + Nemopteridae) + all other Myrmeleontiformia. Hemerobiiformia are based on the ‘maxillary head’ concept. The ithonid clade Ithonidae/Rapismatidae + Polystoechothidae and the dilarid clade Dilaridae + (Mantispidae + (Rhachiberothidae + Berothidae)) are based on robust criteria. Other relationships remain unclear: Hemerobiidae + Chrysopidae (on similarity) and the ‘early offshoot’ concept of coniopterygidae (on autapomorphies) should not be perpetuated. Chysopidae + Osmylidae and (Hemerobiidae + (Coniopterygidae + Sisyridae)) + dilarid clade are discussed. Aquatic larvae, regarded as independent apomorphies of megaloptera and neuropteran Nevrorthidae and Sisyridae for a long time, are re‐interpreted as a synapomorphy of Megaloptera + Neuroptera and thus plesiomorphic within these groups. Terrestrial larvae (with cryptonephry to solve osmotic problems) are consequently apomorphic. Aquatic Sisyridae with cryptonephry of a single malpighian tubule, is conflicting, but larvae may have become secondarily aquatic, after a terrestrial intermezzo.     

Phylogeny of Ptychopteroidea (Insecta: Diptera)

A phylogenetic tree is proposed for the superfamily Ptychopteroidea, reconstructed taking into account both extinct and extant taxa and based mainly on characters of wing venation.     

Phylogeny of Oestridae (Insecta: Diptera)

The phylogeny of Oestridae was analysed at the generic level using 118 characters from all developmental stages and including morphology, ontogeny, physiology and behaviour. Four major clades were given subfamilial rank with the phylogenetic relationship (Cuterebrinae (Gasterophilinae (Hypodermatinae + Oestrinae))). The subdermal parasites of the African elephant, Neocuterebra squamosa Grünberg and Ruttenia loxodontis Rodhain, had their most probable affiliation subordinate to the clade of stomach parasites, although their exact position needs further investigation. Genus Ochotonia Grunin, which is known from a single third‐instar larva only, was the probable sister group of all other Hypodermatinae. Twenty‐five oestrid genera were recognised as valid and those containing more than one species were defined through lists of autapomorphies. Cuterebra Clark was proposed as a senior synonym of Alouattamyia Townsend, Andinocuterebra Guimarães, Pseudogametes Bischof and Rogenhofera Brauer. The clade of hypodermatine ungulate parasites (Hypoderma Latreille +Pallasiomyia Rubtzov +Pavlovskiata Grunin +Przhevalskiana Grunin +Strobiloestrus Brauer) remained largely unresolved, and genus Przhevalskiana emerged without defining characters.     

Evolutionary scenarios for unusual attachment devices of Phasmatodea and Mantophasmatodea (Insecta)

Abstract.  The distal parts of the legs of representatives of Phasmatodea and Mantophasmatodea were examined. The condition found in Mantophasma zephyra and Timema nevadense is described in detail. In both species the arolium is highly modified, i.e. strongly enlarged and pan-shaped and densely covered with acanthae. The presence of acanthae on the euplantulae is another very unusual feature shared by the two taxa. A cladistic analysis based mainly on a data matrix from an earlier study of the authors was carried out, with the inclusion of three new characters derived from attachment devices. The results suggest three possible evolutionary scenarios for the features in question. If Phasmatodea are the sister group of Mantophasmatodea, the apomorphic features of the attachment devices may be synapomorphies of both groups, with different degrees of reversal within the suborder Euphasmatodea. A branching pattern Phasmatodea + (Mantophasmatodea + Grylloblattodea) is consistent with the presence of an enlarged pan-shaped arolium and euplantulae with acanthae in the common ancestor of this lineage, with reversal in Grylloblattodea and within Euphasmatodea. The acanthae on the surface of the arolium may or may not have evolved independently in Timema . A placement of Phasmatodea as sister taxon of Orthoptera, Dictyoptera, or a clade comprising both groups implies that the features in question have evolved independently in phasmids and Mantophasmatodea.     

Phylogeny of the treehoppers (Insecta: Hemiptera: Membracidae): evidence from two nuclear genes

We present a molecular systematic investigation of relationships among family-group taxa of Membracidae, comprising nearly 3.5 kb of nucleotide sequence data from the nuclear genes elongation factor-1alpha (EF-1alpha: 958 bp) and 28S ribosomal DNA (28S rDNA: 2363 bp); data partitions are analyzed separately and in combination for 79 taxa. Analysis of the combined sequence data provided a better-resolved and more robust hypothesis of membracid phylogeny than did separate analyses of the individual genes. Results support the monophyly of the family Membracidae and indicate the presence of two major lineages (Centrotinae + Stegaspidinae + Centrodontinae and Darninae + Membracinae + Smiliinae). Within Membracidae, molecular data support the following assertions: (1) the previously unplaced genera Antillotolania and Deiroderes form a monophyletic group with Microcentrini; (2) Centrodontini and Nessorhinini are monophyletic clades that arise independently from within the Centrotinae; (3) Centrotinae is paraphyletic with respect to Centrodontinae; (4) the subfamily Membracinae is monophyletic and possibly allied with the darnine tribe Cymbomorphini; (5) the subfamily Darninae is paraphyletic; (6) the subfamily Smiliinae is paraphyletic, with molecular evidence indicating the exclusion of Micrutalini and perhaps Acutalini and Ceresini; and (7) Membracidae arose and diversified in the New World with multiple subsequent colonizations of the Old World. Our phylogenetic results suggest that morphology-based classifications of the Membracidae need to be reevaluated in light of emerging molecular evidence.