Head anatomy of adult Sisyra terminalis (Insecta: Neuroptera: Sisyridae) – Functional adaptations and phylogenetic implications

The external and internal head anatomy of Sisyra terminalis is described in detail and compared with data from literature. A salivary pump consisting of a peculiar reservoir and a hitherto unknown muscle, M. ductus salivarii, is newly described for Neuroptera. The upward folded paraglossae form a secondary prolongation of the salivary system. These structures are discussed as functional adaptations for feeding on aphids and desiccated honeydew. In a phylogenetic analysis the basal position of the Sisyridae within Neuroptera is retrieved. The following new synapomorphies are postulated: (1) for Neuropterida, the presence of a M. submentomentalis and prepharyngeal ventral transverse muscles, and the absence of a M. submentopraementalis; (2) for Neuroptera and Sialidae, the presence of a mandibular gland; (3) for Neuroptera, the presence of four scapopedicellar muscles; (4) for Neuroptera exclusive Nevrorthidae and Sisyridae, the weakening of dorsal tentorial arms, the presence of a M. tentoriomandibularis medialis superior and the shifted origin of M. tentoriocardinalis.     

Cladistic analysis of Neuroptera and their systematic position within Neuropterida (Insecta: Holometabola: Neuropterida: Neuroptera)

A phylogenetic analysis of Neuroptera using thirty‐six predominantly morphological characters of adults and larvae is presented. This is the first computerized cladistic analysis at the ordinal level. It included nineteen species representing seventeen families of Neuroptera, three species representing two families (Sialidae and both subfamilies of Corydalidae) of Megaloptera, two species representing two families of Raphidioptera and as prime outgroup one species of a family of Coleoptera. Ten equally most parsimonious cladograms were found, of which one is selected and presented in detail. The results are discussed in light of recent results from mental phylogenetic cladograms. The suborders Nevrorthi‐ formia, Myrmeleontiformia and Hemerobiiformia received strong support, however Nevrorthiformia formed the adelphotaxon of Myrmeleontiformia + Hemerobiiformia (former sister group of Myrmeleontiformia only). In Myrmeleontiformia, the sister‐group relationships between Psychopsidae + Nemopteridae and Nymphidae + (Myrmeleontidae + Ascalaphidae) are corroborated. In Hemerobiiformia, Ithonidae + Polystoechotidae is confirmed as the sister group of the remaining families. Dilaridae + (Mantispidae + (Rhachiberothidae + Berothidae)), which has already been proposed, is confirmed. Chrysopidae + Osmylidae emerged as the sister group of a clade comprising Hemerobiidae + ((Coniopterygidae + Sisyridae) + (dilarid clade)). Despite the sister‐group relationship of Coniopterygidae + Sisyridae being only weakly supported, the position of Coniopterygidae within the higher Hemerobiiformia is corroborated. At the ordinal level, the analysis provided clear support for the hypothesis that Megaloptera + Neuroptera are sister groups, which upsets the conventional Megaloptera + Raphidioptera hypothesis.     

The larval head of Nevrorthidae and the phylogeny of Neuroptera (Insecta)

External and internal head structures of larvae of Nevrorthidae were described in detail. The results were compared to conditions found in other representatives of Neuroptera and the other two neuropterid orders. The cladistic analysis supported the monophyly of Neuroptera, Neuroptera exclusive of Nevrorthidae, Hemerobiiformia, and Myrmeleontiformia. Neuroptera exclusive of Nevrorthidae are supported by the formation of an undivided postmentum and the presence of cryptonephric Malpighian tubules. The highly specialized articulation of the neck (Rollengelenk) and the absence of a salivary duct are autapomorphies of Nevrorthidae. Ithonidae and Polystoechotidae form a clade and are the sister group of the remaining Hemerobiiformia, which are characterized by the complete lack of a gula and a terminal filament of the antenna. Within this lineage, a clade comprising Mantispidae, Dilaridae, Berothidae, and Rhachiberothidae is well supported. Larvae of Myrmeleontiformia are characterized by a complex transformation of head structures, with a hypostomal bridge, a small triangular gula, largely reduced maxillary grooves, and anteriorly shifted posterior tentorial grooves. The slender finger‐like mid‐dorsal apodeme is another autapomorphy of the group. Psychopsidae are placed as the sister group of the remaining Myrmeleontiformia, which are characterized by a conspicuous, protruding ocular region (often less distinct or even absent in Nemopteridae). Ascalaphidae are the sister group of Myrmeleontidae. Larvae of both families share the fusion of the tibia and tarsus in the hind leg. The larval characters analysed were not sufficient for full resolution of the myrmeleontiform and hemerobiiform lineages. The position of several families such as Osmylidae, Sisyridae, and Coniopterygidae remains uncertain. The results are in agreement with an aquatic ancestor of Neuroptera and secondarily acquired terrestrial habits within the lineage (Neuroptera exclusive of Nevrorthidae), and another invasion of the aquatic environment by Sisyridae. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 158 , 533–562.     

The First Mitochondrial Genomes of Antlion (Neuroptera: Myrmeleontidae) and Split-footed Lacewing (Neuroptera: Nymphidae), with Phylogenetic Implications of Myrmeleontiformia

In the holometabolous insect order Neuroptera (lacewings), the cosmopolitan Myrmeleontidae (antlions) are the most species-rich family, while the closely related Nymphidae (split-footed lacewings) are a small endemic family from the Australian-Malesian region. Both families belong to the suborder Myrmeleontiformia, within which controversial hypotheses on the interfamilial phylogenetic relationships exist. Herein, we describe the complete mitochondrial (mt) genomes of an antlion (Myrmeleon immanis Walker, 1853) and a split-footed lacewing (Nymphes myrmeleonoides Leach, 1814), representing the first mt genomes for both families. These mt genomes are relatively small (respectively composed of 15,799 and 15,713 bp) compared to other lacewing mt genomes, and comprise 37 genes (13 protein coding genes, 22 tRNA genes and two rRNA genes). The arrangement of these two mt genomes is the same as in most derived Neuroptera mt genomes previously sequenced, specifically with a translocation of trnC. The start codons of all PCGs are started by ATN, with an exception of cox1, which is ACG in the M. immanis mt genome and TCG in N. myrmeleonoides. All tRNA genes have a typical clover-leaf structure of mitochondrial tRNA, with the exception of trnS1(AGN). The secondary structures of rrnL and rrnS are similar with those proposed insects and the domain I contains nine helices rather than eight helices, which is common within Neuroptera. A phylogenetic analysis based on the mt genomic data for all Neuropterida sequenced thus far, supports the monophyly of Myrmeleontiformia and the sister relationship between Ascalaphidae and Myrmeleontidae.     

The function and phylogenetic implications of the tentorium in adult Neuroptera (Insecta)

Despite several recent analyses on the phylogeny of Neuroptera some questions still remain to be answered. In the present analysis we address these questions by exploring a hitherto unexplored character complex: the tentorium, the internal cuticular support structure of the insect head. We described in detail the tentoria of representatives of all extant neuropteran families and the muscles originating on the tentorium using 3D microCT images and analyzed differences in combination with a large published matrix based on larval characters. We find that the tentorium and associated musculature are a source of phylogenetically informative characters. The addition of the tentorial characters to the larval matrix causes a basad shift of the Sisyridae and clearly supports a clade of all Neuroptera except Sisyridae and Nevrorthidae. A sister group relationship of Coniopterygidae and the dilarid clade is further corroborated. A general trend toward a reduction of the dorsal tentorial arms and the development of laminatentoria is observed. In addition to the phylogenetic analysis, a correlation among the feeding habits, the development of the maxillary muscles, and the laminatentoria is demonstrated.     

The larval morphology of the spongefly Sisyra nigra (Retzius, 1783) (Neuroptera: Sisyridae)

The morphology of mature larvae of Sisyra nigra was studied and documented with a broad spectrum of techniques. Special emphasis is on the cephalic anatomy and on the digestive tract. Cephalic structures are highly modified, with numerous autapomorphic conditions, including a globular head capsule, an extended area with large cornea lenses, a massive tentorium, a strongly developed prepharyngeal pumping apparatus with a horizontal arrangement of dilators, a sharp bend between the prepharynx and pharynx, and an unusual filter apparatus at the entrance of the large crop. The thoracic and abdominal muscle sets, and the legs are largely unmodified. Postcephalic apomorphies are conspicuous tergal setiferous tubercles, trifid setiferous pleural projections, single pretarsal claws, zigzag-shaped abdominal tracheal gills, and a dense vestiture of setae on the terminal abdominal segments. Mandibulo-maxillary stylets curved outwards are an unusual apomorphy also found in the semiaquatic larvae of Osmylidae. Semiaquatic or aquatic habits and secondarily multisegmented antennae are potential synapomorphies of these two groups and Nevrorthidae (Osmyloidea). A sistergroup relationship between Sisyridae and Nevrorthidae suggests that fully aquatic habits of larvae may be a synapomorphy of both families. A specialized terminal antennal seta is a potential groundplan apomorphy of Neuroptera, with secondary loss in Nevrorthidae and Ithonidae + Myrmeleontiformia, respectively. A trumpet-shaped empodium is likely an apomorphy of Neuroptera excluding Coniopterygidae and Osmyloidea, and the secondary loss an apomorphy of Ithonidae on one hand, and Myrmeleontiformia excl. Psychopsidae on the other.     

Phylogenetic relevance of the genital sclerites of Neuropterida (Insecta: Holometabola)

Abstract Segment 9 of male Raphidioptera, comprising tergite, sternite, gonocoxites, gonostyli and gonapophyses, is a benchmark for homologies in the male and female terminalia of the three Neuropterida orders Raphidioptera, Megaloptera and Neuroptera. The segments relating to genitalia are 9, 10 and 11 in males and 7, 8 and 9 in females. Results from holomorphological and recent molecular cladistic analyses of Neuropterida agree in supporting the sister‐group relationships between: (1) the Raphidioptera and the clade Megaloptera + Neuroptera, and (2) the suborder Nevrorthiformia and all other Neuroptera. The main discrepancy between the results of these studies is the nonmonophyly of the suborder Hemerobiiformia in the molecular analysis. The monophyly of the Megaloptera (which has been repeatedly questioned) is further corroborated by a hitherto overlooked ground pattern autapomorphy: the presence of eversible sacs within the complex of the fused gonocoxites 11 in Corydalidae and Sialidae. The recently discovered paired complex of gonocoxites 10 (parameres) in Nipponeurorthus (Nevrorthidae) indicates that the curious apex of sternite 9 of Nevrorthus and Austroneurorthus is the amalgamation of the sclerites of gonocoxites 10 with sternite 9, interpreted as synapomorphic. In the molecular study, the Nevrorthidae, Sisyridae and Osmylidae branch off in consecutive splitting events, a result that is supported by the analysis of male genital sclerites reported here. Extraordinary parallel apomorphies (e.g. excessive enlargement and modification of gonocoxites 10 ending in a thread‐like ‘penisfilum’) in derived representatives of Coniopterygidae, Berothidae, Rhachiberothidae and Mantispidae corroborate the dilarid clade of the morphological analysis and leads us to hypothesize a sister‐group relationship of the Coniopterygidae with the dilarid clade. A re‐interpretation of the tignum of Chrysopidae as gonocoxites 11 means that the structure previously called the gonarcus represents the fused gonocoxites 9. In Hemerobiidae, the corresponding sclerite is consequently also homologized as fused gonocoxites 9. The enlargement of the lateral wings of the gonocoxites in both families is interpreted as a synapomorphy. Excessive enlargement of gonostyli 11 in the Polystoechotid clade and Myrmeleontiformia supports a sister‐group relationship of these two clades. The occurrence of certain serial homologues of female genitalia structures (gonocoxites and gonapophyses), such as the digitiform processus together with the flat appendices in segment 8 of certain Myrmeleontidae, or the wart‐like processus together with the flat circular sclerites in segment 7 of certain Berothidae, as well as the presence of gonocoxites 8 as pseudosternites in certain Nemopteridae and Coniopterygidae, are probably character reversals. The digitiform processus of tergite 9 (pseudogonocoxites) in Rhachiberothidae and Austroberothella (Berothidae) are either independently developed acquisitions with a function in oviposition, or are homologous sclerites, possibly of epipleurite origin.     

Captopodus poschmanni gen. et sp. nov. a new stem-group arthropod from the Lower Devonian Hunsrück Slate (Germany)

A new arthropod from the Lower Devonian Hunsrück Slate is described on the basis of four specimens. The body of Captopodus poschmanni comprises a head, a trunk with an anal portion. The high number of trunk appendages (≥66 segments) is unusual. The function of one pair of cupola-like structures of the head shield is unclear. The presence of large grasping appendages in the head superficially resembles the ‘short great appendages’ of other euarthropods and grasping appendages of thylacocephalans. The phylogenetic position of the arthropod cannot be determined in detail, though several morphological aspects indicate a phylogenetic position as a stem lineage representative of the Euarthropoda, the morphology of the trunk appendages seem to indicate a more advanced phylogenetic position. This new taxon underlines the exceptional diversity of arthropods within the Hunsrück Slate in comparison to other Devonian fossil sites and highlights the significance of the Hunsrück Slate for the evolution of early arthropods.     

Species richness and composition of Neuroptera in the forests fregments of the Taurus Mountains Range,Turkey

In this study, diversity, species richness and composition of Neuroptera has been studied in the forest edges and fragments in the Taurus Mountain Range, southern Turkey. Sampling for species collection was carried out from April 2017 to September 2018 at different distances from the forest center, i.e., (0–500 m), forest mid-interior (501–1000 m), and forest edge (1001–3000 m). A total of 975 adults were collected frequently belonging to the families Ascalaphidae, Coniopterygidae, and Hemerobiidae from the forest edges while Chrysopidae and Myrmeleontidae were most common along the mid-interior regions of the forest. Majority of adutls caught from the mid-interior region comprised of female adults while the males of most species were abundant along the forest edges. Although the forest center shows the largest value for the Dominance species-diversity index and the smallest value for the Shannon index, forest edge was found highest for the Simpson index. The abundance of Neuroptera decreased with wind speed but increased with the temperature in the edge regions. Principal Component Analysis (PCA) indicated that some environmental and habitat variables, e.g. wind speed, temperature, and distance to the forest center, mid-interior and edge, accounted for species distribution patterns in Neuroptera. In the forest center, a linear correlation between wind speed, temperature and specimen abundance was recorded, while these factors were found negatively correlated with specimens abundance in the mid-interior regions of the forest.     

Neuropteroidea--different ovary structure in related groups

Three different ovariole types have been described in the Neuropteroidea. In this review, comparative analysis of their structure and function is presented, and the results are used for phylogenetic considerations. Neuropteran polytrophic ovaries exhibit deviations from the basic polytrophic pattern found in other insects. Asynchronous divisions of germ cells result in a variable and unfixed number of cystocytes per cluster. In contrast to the typically branched system, spatial organization of the cystocyte connections in neuropteran egg chambers is almost linear. A more precise comparative study of ovariole structure and function within Neuroptera brings further support for the placement of Coniopterygidae as an early off-shoot from the main neuropteran phylogenetic lineage. Ovaries of Raphidioptera and Megaloptera: Sialidae represent a distinct type of telotrophic organization. Its almost identical character in both groups favours the concept on the origin of this telotrophy from the common ancestral polytrophic condition. Ovarioles of Megaloptera: Corydalidae are neopanoistic and it is emphasized here that this organization must have evolved independently from the polytrophic background. A hypothesis on paraphyletic origin of Megaloptera is thus supported.     

Mitochondrial phylogenomics illuminates the evolutionary history of Neuropterida

Neuroptera (lacewings) and allied orders Megaloptera (dobsonflies, alderflies) and Raphidioptera (snakeflies) are predatory insects and together make up the clade Neuropterida. The higher‐level relationships within Neuropterida have historically been widely disputed with multiple competing hypotheses. Moreover, the evolution of important biological innovations among various Neuropterida families, such as the origin, timing and direction of transitions between aquatic and terrestrial habitats of larvae, remains poorly understood. To investigate the origin and diversification of lacewings and their allies, we undertook phylogenetic analyses of mitochondrial genomes of all families of Neuropterida using Bayesian inference, maximum likelihood and maximum parsimony methods. We present a robust, fully resolved phylogeny and divergence time estimation for Neuropterida with strong statistical support for almost all nodes. Mitochondrial sequence data are typified by significant compositional heterogeneity across lineages, and parsimony and models assuming homogeneous rates did not recover Neuroptera as monophyletic. Only a model accounting for compositional heterogeneity (i.e. CAT‐GTR) recovered all orders of Neuropterida as monophyletic. Significant findings of the mitogenomic phylogeny include recovering Raphidioptera as sister to Megaloptera plus Neuroptera. The sister family of all other lacewings are the dusty‐wings (Coniopterygidae), rather than Nevrorthidae. Nevrorthidae are instead returned to their traditional position as the sister group of the spongilla‐flies (Sisyridae) and closely related to Osmylidae. Our divergence time analysis indicates that the Mesozoic was indeed a ‘golden age’ for lacewings, with most families of Neuropterida diverging during the Triassic and Jurassic and all extant families present by the Early Cretaceous. Based on ancestral character state reconstructions of larval habitat we evaluate competing hypotheses regarding the life style of early neuropteridan larvae as either aquatic or terrestrial.     

A Remarkable New Family of Jurassic Insects (Neuroptera) with Primitive Wing Venation and Its Phylogenetic Position in Neuropterida

Background

Lacewings (insect order Neuroptera), known in the fossil record since the Early Permian, were most diverse in the Mesozoic. A dramatic variety of forms ranged in that time from large butterfly-like Kalligrammatidae to minute two-winged Dipteromantispidae.

Principal Findings

We describe the intriguing new neuropteran family Parakseneuridae fam. nov. with three new genera and 15 new species from the Middle Jurassic of Daohugou (Inner Mongolia, China) and the Early/Middle Jurassic of Sai-Sagul (Kyrgyzstan): Parakseneura undula gen. et sp. nov., P. albomacula gen. et sp. nov., P. curvivenis gen. et sp. nov., P. nigromacula gen. et sp. nov., P. nigrolinea gen. et sp. nov., P. albadelta gen. et sp. nov., P. cavomaculata gen. et sp. nov., P. inflata gen. et sp. nov., P. metallica gen. et sp. nov., P. emarginata gen. et sp. nov., P. directa gen. et sp. nov., Pseudorapisma jurassicum gen. et sp. nov., P. angustipenne gen. et sp. nov., P. maculatum gen. et sp. nov. (Daohugou); Shuraboneura ovata gen. et sp. nov. (Sai-Sagul). The family comprises large neuropterans with most primitive wing venation in the order indicated by the presence of ScA and AA1+2, and the dichotomous branching of MP, CuA, CuP, AA3+4, AP1+2. The phylogenetic position of Parakseneuridae was investigated using a phylogenetic analysis of morphological scoring for 33 families of extinct and extant Neuropterida combined with DNA sequence data for representatives of all extant families. Parakseneuridae were recovered in a clade with Osmylopsychopidae, Prohemerobiidae, and Ithonidae.

Conclusions/Significance

The presence of the presumed AA1+2 in wings of Parakseneuridae is a unique plesiomorphic condition hitherto unknown in Neuropterida, the clade comprising Neuroptera, Megaloptera, Raphidioptera. The relative uncertainty of phylogenetic position of Parakseneuridae and the majority of other families of Neuroptera reflects deficient paleontological data, especially from critical important periods for the order, earliest Triassic and latest Triassic/earliest Jurassic.     

The karyotypes ofMicroseris bigelovii,M. douglasii,andM. pygmaea (Asteraceae)

The karyotypes of the three annuals,Microseris bigelovii, M. douglasii andM. pygmaea, consist of 2n = 18, small, submetacentric chromosomes. Length, centromere position, C-banding pattern, silver staining of NOR's, and the use of base specific fluorochromes, allow the identification of four of the nine chromosome pairs. The banding pattern ofM. bigelovii andM. pygmaea is identical, but intraspecific differences are found between strains ofM. douglasii.     

Developmental stages of the hooded beetle Sericoderus lateralis (Coleoptera: Corylophidae) with comments on the phylogenetic position and effects of miniaturization

The first detailed morphological study of larvae, pupae and adults of a species of the hooded beetles (Coleoptera: Corylophidae) – Sericoderus lateralis – is presented. Histological sectioning, scanning and transmission electron microscopy, laser confocal microscopy and 3D-computer reconstruction were used. For the first time we report that according to the morphometric data of S. lateralis, at least some corylophid beetles have three larval stages. A phylogenetic position of Corylophidae within a cucujoid-cleroid clade is confirmed, and also the placement of Sericoderini within a corlyophid subgroup, which does not include Periptycinae and Foadiini. The larvae of Sericoderus are mainly characterized by plesiomorphic features compared to those of other corylophid tribes, notably Peltinodini and Rypobiini. Morphological and developmental consequences of miniaturization are discussed. Corylophid beetles display much less specific and far-reaching morphological consequences of miniaturization compared to Ptiliidae. We report the presence of unique modifications in the neural system not shared with any other insects, such as a distinctly asymmetric supraoesophageal ganglion in first instar larva, and a total displacement of the brain to the thorax in the adult stage. A highly unusual feature of the digestive tract is the sclerotised, V-shaped ventral wall of the pharynx. Developmental and size dependent changes in the relative volume of different organs are addressed. All organ systems change allometrically in the development of S. lateralis. Allometric trends in the volume of organs confirm that the factors limiting miniaturization are the size of the neural system, associated with the number and size of neurons (most critical for first instar larva), the mass of the skeleton, the egg size, and consequently the volume of the reproductive system (for free-living insects).     

The mitochondrial genome of Gatzara jezoensis (Neuroptera: Myrmeleontidae) and phylogenetic analysis of Neuroptera

Phylogenetic relationship within Neuroptera is controversial, particularly for the various hypotheses based on both morphological and molecular evidence. In the present study, we determined the complete mitochondrial genome (mitogenome) of Gatzara jezoensis, which is the second representative of the tribe Dendroleontini. The G. jezoensis mitogenome contained the conserved set of 37 mitochondrial genes and a putative control region, with a conserved gene arrangement which was similar to that of most sequenced neuropteran mitogenomes. All transfer RNAs exhibited the canonical cloverleaf secondary structure, except for trnS^(AGN). The control region contained two conserved elements (ploy-T stretch and ATGGTTCAAYAAAATAAYYCYCTC motif) and abundant microsatellite-like elements. The phylogenetic analysis of sequenced neuropteran mitogenomes using the concatenated protein-coding genes (PCGs) and ribosomal genes recovered the monophyly of Myrmeleontidae, which revealed this dataset could generate the more robust phylogeny of Neuroptera than that of 13 PCGs dataset.     

Queens defense by workers in the highly polygynous ant Crematogaster pygmaea (Hymenoptera: Myrmicinae)

Some aspects of the biology of Crematogaster pygmaea, a highly polydomous and polygynous ant, are more commonly found in monogynous species. One such characteristic is the high attractiveness of its queens. In this study, this attractiveness was assessed under varying experimental conditions to investigate the factors responsible for its expression and variation, and to identify the nature of queen attractiveness. It was shown (1) that C. pygmaea queens are highly attractive to the workers that cluster on and around them (retinue), (2) that the attractiveness of C. pygmaea queens is context-dependent, i.e., it increases with increasing degree of potential danger to the queen, (3) that the attractiveness signal of C. pygmaea queens is chemically based, and (4) that this signal is persistent and apparently not colony-specific. The proposed hypothesis is that the C. pygmaea queens constantly release an attractiveness signal that is “read” by the workers, in a dependent way linked to the context, and that the main function of this attractiveness is to protect queens. This protection would have a high adaptive value in the context of the social structure and the reproductive strategies in C. pygmaea.     

Morphological Comparison of Second-Stage Juveniles of Six Populations of Meloidogyne hapla by SEM

External morphology of second-stage juveniles of six populations of Meloidogyne hapla, hclonging to two cytological races (A and B), and one population each of M. arenaria, M. incognita, and M. javanica was compared by scanning electron microscopy (SEM). Race A of M. hapla included three facultatively parthenogenetic populations with haploid chromosome numbers of 15. 16, and 17; race B consisted of three mitotically parthenogenetic populations with somalic chromosome numhers of 45, 45, and 48. The mitotically parthenogenetic populations of M. arenaria, M. incognita, and M. javanica had 54, 41-43, and 44 chromosomes, respectively. Observations were made on head structures, lateral field, excretory pore, anal opening, and tail. Head morphology, including shape and proportion of labial disc and lips, expression of labial and cephalic sensilla, and markings on head region, was distinctly different for each species. M. hapla populations of race A were distinct from each other but showed much intrapopulatiou variation in head morphology. Populations of race B were different from those of race A and were very stable and quite similar in head morphology. Considerable inter- and intrapopulatiou variation made the structure of the lateral field, excretory pore, anal opening, and tail of little value in distinguishing species or populations. The results are discussed in relation to earlier SEM observations on the genus Helerodera.     

Status of Charidotis pygmaea (Coleoptera: Chrysomelidae) as a Biological Control Agent of Lantana montevidensis (Verbenaceae) in Australia

The establishment of the leaf-feeding beetle Charidotis pygmaea Klug and its potential to control Lantana montevidensis (Sprengel) Briquet, a serious pasture weed of central and southern Queensland, Australia, were assessed. C. pygmaea was collected in Brazil from Lantana fucata Lindley, a plant morphologically similar to L. montevidensis. Over 40,000 beetles were released over 3 years by use of caged and uncaged techniques at 25 sites throughout southeast and central Queensland. At 6 of the sites where detailed and frequent monitoring occurred, no adults were found 6 months after the release. At another 2 sites, adults were present for only 12 months. Only a small number of eggs were laid at any single site and few larvae completed development to the adult stage. No signs of insect activity were found at any site after 24 months. Comparative laboratory and experimental field plot trials with both the weedy (field host) and the ornamental (glasshouse host) forms of L. montevidensis did not show significant differences in insect performance. Assessment of nitrogen, phosphorous, potassium, and water contents, leaf hairiness, and leaf toughness of both the weedy and the ornamental forms of L. montevidensis grown under glasshouse and field plot conditions did not show differences between the two plant forms. There were, however, differences in the percentage of adults that developed in the glasshouse trials compared to the field plot trials (55% vs 5%). Field observations in Brazil showed that C. pygmaea was found only on L. fucata and L. tiliifolia Chamisso and was not seen on L. montevidensis growing in the same region. Climate matching with CLIMEX showed that most areas in Australia where L. montevidensis is a major problem are not climatically similar to the collection sites of C. pygmaea in Brazil. Whereas populations of C. pygmaea can be maintained on L. montevidensis under glasshouse conditions, it performs poorly on that species under field conditions. Unsuitable climatic conditions and an incompatible target plant are the most likely factors affecting the poor performance of C. pygmaea. Consequently, field releases of the agent in Australia have ceased and C. pygmaea is not recommended as a biological control agent for L. montevidensis in Australia.