Phylogenetic position of rhyacophiloid caddisflies (Insecta, Trichoptera): a spermatological analysis of Rhyacophilidae and Glossosomatidae

Most caddisflies (Insecta, Trichoptera) are classified into two suborders, Annulipalpia and Integripalpia. However, the use of the derived characters that are regularly applied in systematic and phylogenetic analyses of Trichoptera is insufficient to determine with certainty the position of the families belonging to Rhyacophiloidea, which are considered by different authors to be either Annulipalpia, or Integripalpia, or even a separate suborder. Rhyacophiloidea comprise four overall similar families: free-living Rhyacophilidae and Hydrobiosidae, saddle-case making Glossosomatidae, and purse-case making Hydroptilidae. It was previously found that Annulipalpia spermatozoa have aberrant axonemes while Integripalpia spermatozoa display the plesiomorph 9 + 2 axoneme. The present spermatological analysis of the families Rhyacophilidae and Glossosomatidae shows that both have spermatozoa with aberrant axonemes lacking the two central microtubules found in the typical axoneme of insect spermatozoa. This is an apomorphic character shared with the superfamily Hydropsychoidea, indicating that from this point of view, Rhyacophiloidae are more closely related to Annulipalpia than to Integripalpia.     

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.     

Waxes and lipids associated with the external waxy structures of nymphs and pupae of the giant whitefly, Aleurodicus dugesii

The nymphs and pupae of the giant whitefly, Aleurodicus dugesii, produce large quantities of external lipids, both as waxy particles and as waxy filaments. The nymphs and pupae extrude filaments from two dorsal rows of five pores each. Filaments can attain lengths of 5-8 cm. The external lipids of nymphs and pupae consist largely of long-chain aldehydes, alcohols, acetate esters and wax esters. Hydrocarbons are minor components. Soon after hatching, the nymph produced an unidentified waxy fringe extruded laterally from its margin. After molting to the second instar, long, hollow, waxy filaments were produced by the immature stages. The major lipid class associated with the filaments was saturated wax esters (89%), mainly C44, C46 and C60. Associated with formation of the filaments were waxy particles in the shape of curls, which peeled off of the extruding filaments. Similar but more tubular-shaped curls were also produced by numerous lateral pores so that, eventually, the curls completely camouflaged the nymph. The major lipid class of the curls was wax esters (50%), mainly C44 and C46. The cuticular surface lipids of the nymphs were mainly long-chain aldehydes (43%) and wax esters (27%). Unsaturated fatty acid moieties constituted 2 and 19% of the wax esters of curls and nymph cuticular surface lipids, respectively. The major lipid classes of pupae and of their palisade were long-chain aldehydes and alcohols. No unsaturated wax esters were detected in the filaments, but 30% of pupal and 21% of palisade surface wax esters were unsaturated in their fatty acid moieties, 16:1, 18:1 and 20:1.     

A multigene phylogeny and timeline for Trichoptera (Insecta)

The Trichoptera, or caddisflies, are traditionally split into two taxonomic subdivisions: the ‘retreat-making’ Annulipalpia and the ‘case-making’ Integripalpia (sensu Ross). The monophyly of these groups is well documented; however, the establishment of a third subdivision, ‘Spicipalpia’, and the positions of the five ‘spicipalpian’ families is much debated. In contrast to previous molecular studies using nuclear ribosomal RNA, a recent trichopteran study (using nuclear protein-coding genes) placed one of these ‘spicipalpian’ families, the free-living predatory Rhyacophilidae, as the sister taxon to the rest of Trichoptera, a result that has significant implications for both the understanding of trichopteran evolution and its timing. This paper sets out to investigate the relationships of Trichoptera using several newly sequenced genes, together with previously published gene sequences. This dataset is the largest trichopteran dataset to date, covering six independent genes and > 10 000 nucleotides, and containing 185 species representing 49 families. With all data included, likelihood and Bayesian analyses support a monophyletic Annulipalpia and a monophyletic Integripalpia, which includes the ‘spicipalpians’ as a paraphyletic grade at the base of this clade. However, an analysis of the protein-coding data alone using similar analytical methods recovers Rhyacophilidae as the most basal taxon in Trichoptera, with low support. A reanalysis correcting for nucleotide composition bias provides support for the placement of the ‘spicipalpian’ taxa as sister to the Integripalpia, consistent with the total data analysis, suggesting that the basal position of Rhyacophilidae in the uncorrected analysis could be (or is probably) an artefact of base composition. We find it likely that ancestral trichopterans made incipient cases and retreats, and these had independent origins as precocious pupal chambers. Molecular dating analysis in beast , using the birth-death model of speciation, with a relaxed-clock model of sequence evolution informed by 37 fossil constraints, suggests that the most recent common ancestor of Trichoptera appeared in the Permian (c. 275 Ma) in line with the first appearance of Trichoptera in the fossil record, and that vicariance explains the distribution of most trichopteran taxa. A new infraordinal name, Phryganides , is introduced for the tube-case-making families of Integripalpia.     

Sperm structure of Trichoptera. IV. Rhyacophilidae and Glossosomatidae

The families Rhyacophilidae and Glossosomatidae (Trichoptera) are considered to be the most primitive ones within the order. We examined the spermatozoa of members of these families to see whether their ultrastructure is consistent with an ancestral position. Axonemal structures, after fixation with a tannic acid-containing fixative, have been shown to be particularly useful as taxonomical indicators. It was found that 4 members of Rhyacophilidae, representing 3 subgenera (Rhyacophila, Pararhyacophila, and Hyporhyacophila) all have motile spermatozoa, with a 9 + 9 + 2 axoneme in which inner (but no outer) dynein arms are present. The accessory tubules have a wall consisting of 17 protofilaments, decreasing to 16 near the distal end, whereas the examined member of Glossosomatidae, Catagapetus nigrans, has accessory tubules with 18 protofilaments and a 9 + 9 + 2 axoneme with inner dynein arms and with motility similar to the Rhyacophilidae. Sperm motility is consistent with the inclusion of these 2 families within the suborder Integripalpia, and the axonemal pattern 9 + 9 + 2 indicates that the families indeed occupy a primitive position within Trichoptera.     

The evolutionary history of Trichoptera (Insecta): A case of successful adaptation to life in freshwater

The insect order Trichoptera (caddisflies) forms the second most species‐rich monophyletic group of animals in freshwater. So far, several attempts have been made to elucidate its evolutionary history with both morphological and molecular data. However, none have attempted to analyse the time frame for its diversification. The order is divided into three suborders – Annulipalpia, Integripalpia and ‘Spicipalpia’. Historically, the most problematic taxon to place within the order is ‘Spicipalpia’, whose larvae do not build traditional cases or filtering nets like the majority of the caddisflies. They have previously been proposed to be the sister group of all other Trichoptera or more advanced within the order, with equivocal monophyly and with different interordinal placements among various studies. In order to resolve the evolutionary history of the caddisflies as well as timing their diversification, we utilized fragments of three nuclear (carbamoylphosphate synthethase, isocitrate dehydrogenase and RNA polymerase II) and one mitochondrial (cytochrome oxidase I) protein coding genes, with 16 fossil trichopteran taxa used for time calibration. The ‘spicipalpian’ families are recovered as ancestral to all other caddisflies, though paraphyletic. We recover stable relationships among most families and superfamilies, resolving many previously unrecognized phylogenetic affinities amongst extant families. The origin of Trichoptera is estimated to be around 234 Ma, i.e. Middle – Late Triassic.     

INCORPORATION OF FRESHWATER RHODOPHYTA INTO THE CASES OF CADDISFLIES (TRICHOPTERA) FROM NORTH AMERICA

Cases of larvae and pupae from six caddisfly (Insecta, Trichoptera) genera in three families from North America were observed to contain pieces of freshwater rhodophyte thalli. Seven genera of Rhodophyta, representing 13 species and 35 populations, were observed in this association. Four of the 25 species of Batrachospermum were incorporated into cases of Ochrotrichia ( Hydroptilidae) and Agrypnia ( Phryganeidae). Two of the three freshwater species of Bostrychia were used by Ochrotrichia larvae. Both Compsopogon coeruleus ( Balbis) Mont. and C. prolificus Yadava et Kumano were present in the cases of Hydroptial ( Hydroptilidae) and Ochrotrichia; Compsopogonopsis leptocladus ( Mont.) Krishnamur-thy was observed in the cases of Hydroptila. The more cartilaginous thalli of Lemanea fluviatilis ( L.) C. Ag. and Tuomeya americana ( Kütz.) Papenfuss were used by the brachycentrid larvae of Brachycentrus and Mi-crasema. Lemanea and Paralemanea spp. were also in the cases of Dibusa angata Ross (Hydroptilidae). The architecture of each caddisfly case was studied with light and scanning electron microscopy. Strips of algae were fit together in a transverse, concentric, or spiralled fashion. Based on transmission electron micrographs, cortical cells of Lemanea and Tuomeya in the cases of Brachycentrus and Micrasema appeared to be healthy with intact chloroplasts and typical batrachospermalean pit plugs. Geographic distributions of each rhodophyte-caddisfly association are given .     

九华河水生昆虫群落结构和水质生物评价价

1989年6月、8月、10月对安徽九华河水系3、4、5级支流5个基点采用扫网、刷石等综合定性取样法,共采得水生昆虫9目、49科、86属、124种,计6445头。其中:毛翅目12科、41种;蜉蝣目10科、26种;鞘翅目5科、16种;双翅目7科、14种;襀翅目4科、9种;蜻蜓目5科、8种;半翅目4科、5种;广翅目1科、3种;鳞翅目1科、2种。3、4级支流Shannon多样性指数大于4,种丰富度大于60,水质极清洁;5级支流Shannon多样性指数大于3,种丰富度29,水质较清洁。3级支流以毛翅目,蜉蝣目为主,科级水平生物指数最高(2.58—2.59);4级支流以毛翅目、蜉蝣目和双翅目为主,多样性指数最高(5.54);5级支流以蜉蝣目、双翅目为主。本文还根据“河流连续概念”对各支流水生昆虫群落结构、季节性变化、毛翅目取食功能类群与支流级别的关系等作了初步分析,并提供了必要的物理、化学参数。     

毛翅目化石研究进展

本文详细总结和回顾了世界毛翅目化石研究简史,列出已发表的化石种类名录、分布及年代,共37科、193属、661种(包括中国发现的4科9属15种),描述了不同地质时期主要毛翅目化石的分类单元和分布地区。简要介绍了毛翅目分类系统及系统发育、不同地质时期毛翅目化石的产地及时代。初步分析了目前该类群所存在的一些问题,并对今后的研究工作进行了展望。     

On the fauna of chironomidae (Diptera) of the Hrazdan Basin (Armenia)

A faunistic review of larvae and pupae of chironomid midges (Diptera, Chironomidae) from 15 habitats in the Hrazdan River valley (Armenia) is presented. The revealed fauna includes 40 species from 20 genera and 6 families and tribes. Diploid chromosome numbers are specified for 24 species from 13 genera and 4 subfamilies; 23 species from 14 genera and 4 subfamilies are reported from the region for the first time. Predominant oligotrophic status is confirmed for most of the reservoirs studied.     

Phylogenetic relationships among the lepidopteran and trichopteran suborders (Insecta) from the embryological standpoint1

Adopting the cladistic method in comparative embryology, 27 embryonic characters were analyzed to reconstruct the phylogenetic relationships among the lepidopteran and trichopteran suborders, viz., Annulipalpia, Integripalpia, Zeugloptera, Dacnonypha, Exoporia, Monotrysia, and Ditrysia. The resultant cladogram is basically coincident with that proposed by Kristensen . The order Trichoptera and Lepidoptera constitute a monophyletic group on the basis of one synapomorphy, the presence of well developed silk glands in embryos. The Trichoptera are separable from the Lepidoptera by the states of four characters. The Trichoptera, as a whole, are quite homogenous, and embryological data provide no rational ground for the separation of this order into the Annulipalpia and Integripalpia at a subordinal level. On the contrary, the embryonic development of the Lepidoptera becomes divergent from the most primitive condition to a specialized one according to suborders. The Zeugloptera are the sister group of all other Lepidoptera, because they share two apomorphies with the latter. The Dacnonypha are the most primitive next to the Zeugloptera, and have a sister-group relationship with the Exoporia + (Monotrysia + Ditrysia), being held together with the latter by five synapomorphies. Although the Exoporia retain almost as many plesiomorphic characters as the Dacnonypha, they have a sister-group relationship with the Monotrysia + Ditrysia, as inferred on the basis of two synapomorphies. The Monotrysia and Ditrysia have a sistergroup relationship, and are the most advanced groups in the Lepidoptera judging from their shared acquisition of many apomorphic characters.     

Comparative and functional morphology of wing coupling structures in Trichoptera: Annulipalpia

Several orders of morphologically four‐winged insects have evolved mechanisms that enforce a union between the mesothoracic and metathoracic wings (forewings and hindwings) during the wing beat cycle. Such mechanisms result in a morphologically tetrapterous insect flying as if it were functionally dipterous, and these mechanisms have been described for several insect orders. The caddisfly suborders Annulipalpia and Integripalpia (Trichoptera) each have evolved a wing coupling apparatus, with at least three systems having evolved within the suborder Annulipalpia. The comparative and inferred functional morphology of the putative wing coupling mechanisms is described for the annulipalpian families Hydropsychidae (subfamilies Macronematinae and Hydropsychinae), Polycentropodidae and Ecnomidae, and a novel form‐functional complex putatively involved with at‐rest forewing‐forewing coupling is described for Hydropsychidae: Smicrideinae. It is proposed that the morphology of the wing coupling apparatuses of Hydropsychinae and Macronematinae are apomorphies for those clades. J. Morphol. 2009. © 2009 Wiley‐Liss, Inc.     

Global diversity of caddisflies (Trichoptera: Insecta) in freshwater

The not yet uploaded Trichoptera World Checklist (TWC) [], as at July 2006, recorded 12,627 species, 610 genera and 46 families of extant and in addition 488 species, 78 genera and 7 families of fossil Trichoptera. An analysis of the 2001 TWC list of present-day Trichoptera diversity at species, generic/subgeneric and family level along the selected Afrotropical, Neotropical, Australian, Oriental, Nearctic and Palaearctic (as a unit or assessed as Eastern and Western) regions reveals uneven distribution patterns. The Oriental and Neotropical are the two most species diverse with 47–77% of the species in widespread genera being recorded in these two regions. Five Trichoptera families comprise 55% of the world’s species and 19 families contain fewer than 30 species per family. Ten out of 620 genera contain 29% of the world’s known species. Considerable underestimates of Trichoptera diversity for certain regions are recognised. Historical processes in Trichoptera evolution dating back to the middle and late Triassic reveal that the major phylogenetic differentiation in Trichoptera had occurred during the Jurrasic and early Cretaceous. The breakup of Gondwana in the Cretaceous led to further isolation and diversification of Trichoptera. High species endemism is noted to be in tropical or mountainous regions correlated with humid or high rainfall conditions. Repetitive patterns of shared taxa between biogeographical regions suggest possible centres of origin, vicariant events or distribution routes. Related taxa associations between different regions suggest that an alternative biogeographical map reflecting Trichoptera distribution patterns different from the Wallace (The Geographical Distribution of Animals: With a Study of the Relations of Living and Extinct Faunas as Elucidating the Past Changes of the Earth’s Surface, Vol. 1, 503 pp., Vol. 2, 607 pp., Macmillan, London, 1876) proposed biogeography patterns should be considered. Anthropogenic development threatens biodiversity and the value of Trichoptera as important functional components of aquatic ecosystems, indicator species of deteriorating conditions and custodians of environmental protection are realised.     

Morphology of the mandibles in the millipedes (Diplopoda, Arthropoda)

The mouthparts of seven species from five families of Diplopoda have been investigated with scanning electron microscopy. The distal segment of the mandible, the gnathal lobe, is the most complex structure. Although the biting and crushing parts among the examined genera arc always based on the same general scheme, typical modifications of these structures exist which are regarded to be taxon-specific. The density of the teeth on the pectinate lamellae appears to determine the size of the ingested food particles. A well-developed anterior fringe does not seem to be necessary for the ingestion of food.     

PORE CANALS AND RELATED STRUCTURES IN INSECT CUTICLE

The fine structure and the distribution of an esterase have been studied in the cuticle of Galleria larvae, Tenebrio larvae and pupae, and in the wax-secreting cuticle of the honey bee, and compared with those in the cuticle of the caterpillar of Calpodes. In Galleria and Tenebrio the pore canals are spaces passing through the lamellate endocuticle from the epithelium to the epicuticle. They contain a filament from the cells which may be concerned in their formation. The shape of the pore canal is probably determined by the orientation of the fibres making up the lamellae in the endocuticle and is not a regular helix. The pore canals also contain numerous filaments of another sort which pass on through the epicuticle and are believed to be the origin of the surface wax. They are particularly abundant in the pore canals of the honey bee wax-secreting cuticle and extend into the cell in long pockets surrounded by an envelope of the plasma membrane. The esterase is probably concerned with the final stage of wax synthesis, for its distribution is similar to that of the lipid filaments.     

Massive gene rearrangements of mitochondrial genomes and implications for the phylogeny of Trichoptera (Insecta)

Mitochondrial genomes have been widely used for phylogenetic reconstruction and evolutionary analysis in various groups of Insecta. Gene rearrangements in the mitogenome can be informative characters for phylogenetic reconstruction and adaptive evolution. Trichoptera is one of the most important groups of aquatic insects. Prior to this study, complete mitogenomes from Trichoptera were restricted to eight families, resulting in a biased view of their mitogenome structure and evolution. Here, we assemble new mitogenomes for 66 species by high-throughput sequencing. The mitogenomes of 19 families and 47 genera are documented for the first time. Combined with 16 previously published mitogenomes of Trichoptera, we find 14 kinds of gene rearrangement patterns novel for Trichoptera, including rearrangement of protein-coding genes, tRNAs and control regions. Simultaneously, we provide evidence for the occurrence of tandem duplication and non-random loss events in the mitogenomes of three families. Phylogenetic analyses show that Hydroptilidae was recovered as a sister group to Annulipalpia. The increased nucleotide substitution rate and adaptive evolution may have affected the mitochondrial gene rearrangements in Trichoptera. Our study offers new insights into the mechanisms and patterns of mitogenome rearrangements in Insecta at large and into the usefulness of mitogenomic gene order as a phylogenetic marker within Trichoptera.     

Loss of larval parasitism in parasitengonine mites

Larval Parasitengona are typically parasites, yet at least 29 species of water mites and one species of Trombidiidae forgo larval feeding and any association with a host. Species with non-feeding larvae are isolated cases within species groups or genera where the remaining species have parasitic larvae. Species without larval parasitism occur in at least 14 genera, eight families and four superfamilies of water mites; the loss of larval parasitism is presumably polyphyletic, having occurred at least 21 times. Lineages of water mites with non-feeding larvae frequently exist in parallel with almost identical populations or species that have parasitic larvae. Thus, there is tremendous potential for studies comparing the relative merits of the two life history strategies. Comparisons indicate that adults from lineages with non-parasitic larvae produce smaller numbers of larger eggs; the extra nutrition included in larger eggs permits the larvae to forgo feeding. Non-feeding larvae frequently have wider dorsal plates but reduced leg length, setal length and sclerotization when compared to parasitic larvae from sister lineages. The adults of lineages with non-feeding larvae are frequently smaller in comparison to adults of sister lineages with parasitic larvae. There is no apparent pattern in relation to habitat: lineages lacking larval parasitism occur in streams, temporary ponds and the littoral and planktonic regions of permanent lakes. © Rapid Science Ltd. 1998     

Actin localization in male germ cell intercellular bridges in the rat and ground squirrel and disruption of bridges by cytochalasin D

Filaments about 6-7 nm in diameter were seen associated with germ cell intercellular bridges in detergent-permeabilized cells treated with tannic acid. Approximately 40-50 filaments were present subjacent to the bridge density. Filaments encircled the bridge channel in a manner similar to contractile ring actin filaments of dividing cells. NBD-phallacidin and myosin S-1 subfragments were employed to demonstrate that the filaments observed at intercellular bridges are actin. Intratesticular injection of a single dose of cytochalasin D, a specific inhibitor of actin filaments, caused certain intercellular bridges of spermatids to open within 3 hr after injection, leading to the production of symplasts. During bridge opening, remnants of bridge densities were gradually incorporated into the lateral aspect of the plasma membrane of the symplast. Thus actin, present in bridge structures, appeared to participate in maintaining certain intercellular bridges. A model of intercellular bridge structure is presented.     

The first parasitic Trichoptera

Abstract.

• 1 A parasitoid habit is confirmed in larvae of an Australian micro-caddisfly, Orthotrichia muscari Wells, being the first known incidence of this habit in the order Trichoptera.
• 2 Larvae of O.muscari are non-specific parasites of pupae of other caddisfly species.
• 3 O.muscari is in an Australian/New Guinean/SE Asian species group in Orthotrichia, all members of which probably share the habit. Their larvae and pupae have atypical features that are interpreted as adaptations to their uncharacteristic niche.

     

Phylogenesis of spermatogenesis in Annulipalpia caddisflies: An ultrastructural analysis on philopotamidae spermiogenesis

Characters currently used in phylogenetic analyses are insufficient for determining the status of several families of the order Trichoptera (caddisflies). Comparative spermatology can contribute to solving this problem. In the suborder Integripalpia, the sperm axoneme displays the pattern of 9 + 2 pairs of parallel microtubules found in many animal species. In the suborder Annulipalpia, however, axonemes bear remarkable aberrations. Consistently, in Chimarra florida (Philopotamidae, Annulipalpia) we found that the number of central microtubules varies from zero to four in axonemes of the spermatids and that spermatozoa lack axonemes. We propose that, similarly, the axoneme pattern became unstable in the Annulipalpia ancestor, from which branched two phylogenetic lines having different kinds of axoneme aberrations: (a) families in which the number of central microtubules of the axoneme exceeds two (e.g., Philopotamidae, Polycentropodidae) and (b) families in which the number of central microtubules of the axoneme does not exceed two (e.g., Hydropsychidae).