我国12种蚊幼虫上颚形态和鉴别特征的研究

本文对8种库蚊和按蚊、伊蚊、阿蚊及杵蚊各属代表种的4龄幼虫上颚进行扫描电镜观察.概述了上颚的外部形态,并提出了各蚊种的鉴别特征.指出幼虫上颚具有显著的种间差异,具有重要的分类学意义,讨论了上颚的结构与功能的关系.通过对上颚结构和取食方式的比较研究,从生物学角度,提出蚊科进化关系.     

Modulation in the feeding prey capture of the ant-lion, Myrmeleon crudelis

Ant-lions are pit-building larvae (Neuroptera: Myrmeleontidae), which possess relatively large mandibles used for catching and consuming prey. Few studies involving terrestrial arthropod larva have investigated prey capture behavior and kinematics and no study has shown modulation of strike kinematics. We examined feeding kinematics of the ant-lion, Myrmeleon crudelis, using high-speed video to investigate whether larvae modulate strike behavior based on prey location relative to the mandible. Based on seven capture events from five M. crudelis, the strike took 17.60 ± 2.92?msec and was characterized by near-simultaneous contact of both mandibles with the prey. Modulation of the angular velocity of the mandibles based on prey location was clearly demonstrated. M. crudelis larvae attempted to simultaneously contact prey with both mandibles by increasing mean angular velocity of the far mandible (65 ± 21?rad?sec(-1) ) compared with the near mandible (35 ± 14?rad?sec(-1) ). Furthermore, kinematic results showed a significant difference for mean angular velocity between the two mandibles (P<0.005). Given the lengthy strike duration compared with other fast-striking arthropods, these data suggest that there is a tradeoff between the ability to modulate strike behavior for accurate simultaneous mandible contact and the overall velocity of the strike. The ability to modulate prey capture behavior may increase dietary breadth and capture success rate in these predatory larvae by allowing responsive adjustment to small-scale variations in prey size, presentation, and escape response.     

Sound production and chorusing behaviour in larvae of Icosium tomentosum

Substrate-borne vibrations produced by the larvae of non-lamiinae longicorn Icosium tomentosum Lucas, 1854 (Cerambycidae: Cerambycinae) are also emitted as loud sounds audible to humans. The vibrations consists of a long sequence of regularly repeated pulses at a rate of 8 pulses per second. The duration of the pulses are 0.061±0.009 s and the interpulse intervals are 0.065±0.015 s. The mechanism of vibration generation is the scraping by strongly sclerotised mandibles against the bark. Chorusing behaviour previously unknown in Cerambycidae larvae have been observed when the larvae feeding in the same or nearby branches starting to produce the audible vibrations in reaction to the vibrations of another larva.     

Development and metamorphosis of the feeding apparatus of the stone crab,Menippe mercenaria (brachyura,xanthidae)

Analysis of the feeding apparatus of the stone crab, Menippe mercenaria (Brachyura, Xanthidae), has demonstrated that substantial internal and external morphological alterations occur at metamorphosis and suggests that the mastication of food shifts from the mandibles to the gastric mill at that time. These changes correspond to the changes in environment and diet that take place at metamorphosis, when the previously planktotrophic larvae begin benthic life. A detailed account of the structure and development of the mandibles is presented. The mandibles of all zoeal stages are similar: The incisor process has a series of teeth and denticles and the prominent molar process appears to be well adapted for grinding food. Megalopal mandibles are transitional but have the form that is typical of all subsequent stages: The expanded incisor process is rounded and toothless and the molar process is less prominent and has lost its grinding denticles. The cardiac stomach of the zoeal stages has no gastric mill; the medial and lateral teeth of the mill first appear in the megalopa. A very simple procedure is described for preparing larval mandibles for scanning electron microscopy using the molted exoskeletons from larval rearing experiments.     

External morphology of the larvae of Ephydra (Hydropyrus) hians (Diptera: Ephydridae)

Scanning electron microscopy is used to describe the ultrastructure of morphological features related to feeding, locomotion, respiration, and pigmentation in second- and third-instar larvae of Ephydra hians (Ephydridae: Diptera). Using larvae fixed with the head extended, the ultrastructural details of the mandibles, maxillary papilli, and antennae are described for the first time. The larvae possess finger-like projections at the anterior spiracle and a distensible bifurcated siphon at the posterior spiracle. Slit-like openings are found on each. The second- and third-instar larvae can be differentiated on the basis of dorsal pigmentation associated with extensive patches of spines. The larvae have regional specializations in spine distribution, particularly on the ventral and dorsal body surfaces, and the prolegs. © 1994 Wiley-Liss, Inc.     

Medicago truncatula-derived calcium oxalate crystals have a negative impact on chewing insect performance via their physical properties

Plant structural traits often act as defenses against herbivorous insects, causing them to avoid feeding on a given plant or tissue. Mineral crystals of calcium oxalate in Medicago truncatula Gaertn. (Fabaceae) leaves have previously been shown to be effective deterrents of lepidopteran insect feeding. They are also inhibitors of conversion of plant material into insect body mass during or after consumption. Growth of beet armyworm, Spodoptera exigua Hübner (Lepidoptera: Noctuidae), larvae was correspondingly greater on calcium oxalate‐defective (cod) mutants of M. truncatula with lower levels of crystal accumulation. Data presented here show that insects feeding on M. truncatula leaves with calcium oxalate crystals experience greater negative effects on growth and mandible wear than those feeding on artificial diet amended with smaller amorphous crystals from commercial preparations. Commercial calcium oxalate can be added to insect artificial diet at levels up to 7.5‐fold higher than levels found in wild‐type M. truncatula leaves with minimal effect on insect growth or lepidopteran mandibles. These data suggest that negative impacts of calcium oxalate in the diet of larvae are due to physical factors, and not toxicity of the compound, as high levels of the commercial crystals are readily tolerated. In contrast to the dramatic physical effects that M. truncatula‐derived crystals have on insect mandibles, we could detect no damage to insect peritrophic gut membranes due to consumption of these crystals. Taken together, the data indicate that the size and shape of prismatic M. truncatula oxalate crystals are important factors in determining effects on insect growth. If manipulation of calcium oxalate is to be used in developing improved insect resistance in plants, then our findings suggest that controlling not only the overall amount, but also the size and shape of crystals, could be valuable traits in selecting desirable plant lines.     

The Morphology of the Mandibles in Zoea I Larvae of the Burrowing Shrimp Genera <Emphasis Type="Italic">Upogebia</Emphasis> (Gebiidea) and <Emphasis Type="Italic">Nihonotrypaea</Emphasis> (Axiidea)

The mandibles in the first zoeal stage of five species of the burrowing shrimp genera Upogebia (infraorder Gebiidea) and Nihonotrypaea (infraorder Axiidea) have been examined by scanning electron microscopy. The general shape of the mandibles in Upogebia zoeae is similar to that in Anomura larvae; in Nihonotrypaea, it is intermediate between the mandibles of anomuran and caridean shrimp larvae. The asymmetry of the mandibles, which is more pronounced in Nihonotrypaea, is confirmed. Species-specific features of the structure of the incisor process are found in three Upogebia species, while two Nihonotrypaea species almost do not differ in the mandible structure in their zoea I larvae. The morphological features of the mandibles indicate differences in the diet of Upogebia and Nihonotrypaea larvae. Under natural conditions, zoea I of the studied Nihonotrypaea species may feed on diatoms, which should be taken into account when rearing these decapod larvae in the laboratory.     

Larval host plants of two lizard beetles in the genus Tetraphala (Coleoptera,Erotylidae, Languriinae,Languriini) from Taiwan,with a host plant list of Languriini

Lizard beetles (Erotylidae, Languriinae, Languriini) are known as stem borers of plants and contain agricultural pests and endangered species, but their species–host plant associations have been poorly documented. Here we investigated the larval host plants of two species of the genus Tetraphala Strum, T. collaris (Crotch) and Tetraphala sp. occurring in Taiwan. Females of T. collaris excavated living leafstalks and stems of the herbaceous dicot, Sambucus chinensis (Adoxaceae) using their mandibles for oviposition. We observed the eggs and early-instar larvae inside and nearby oviposition holes and late-instar larvae inside stems, suggesting that T. collaris uses living leafstalks and stems of S. chinensis as oviposition substrate and the larvae tunnel into stems with feeding on the tissues. Similarly, females of Tetraphala sp. excavated living leafstalks of the fern, Pteris wallichiana (Pteridaceae) using their mandibles for oviposition. We observed the eggs and early-instar larvae inside and nearby oviposition holes. When reared in laboratory, a larva reached adulthood inside the leafstalk. These results indicated that Tetraphala sp. uses living leafstalks of Pt. wallichiana as oviposition substrate and the larvae complete their development within. This study revealed that the genus Tetraphala contains both fern- and dicot-users during larval period. Further study is needed to clarify the evolutionary process of host plant use of languriines. Additionally, the host plant list of Languriini is provided.     

Morphometric changes during soldier differentiation of the damp-wood termite Hodotermopsis japonica (Isoptera, Termopsidae)

Summary. To clarify the allometric development of body parts accompanying soldier differentiation in termites, we measured 16 body parts of soldiers, presoldiers, pseudergates (workers), nymphs and larvae of the damp-wood termite Hodotermopsis japonica. Principal component analysis (PCA) was performed using these parameters, which revealed that differentiation into soldiers differed distinctly from development into adult (reproductive) individuals. In particular, the anterior body parts enlarged during development of soldiers. Similarly, elongation of the apical portion of both mandibles was noted during soldier differentiation. X-ray analysis of mandibles revealed sclerotization of the soldier mandibles after differentiation into terminal soldiers. These morphological changes during soldier differentiation are associated with changes in their roles within the colony. Through soldier differentiation, the morphology of this caste of termite becomes functionally suited for attacking predators, and unsuitable for feeding on wood using their mandibles. Based on these data, we suggest that there must be some morphogenetic factors leading caste specific morphology such as soldier mandibles.     

Phylogenetic relationships and the larval head of the lower Cyclorrhapha (Diptera)

We examined final‐stage larvae of all currently recognized lower cyclorrhaphan (= Aschiza) families, except Ironomyiidae and Sciadoceridae, and those of the higher cyclorrhaphan (= Schizophora) families Calliphoridae, Conopidae, Lonchaeidae, Muscidae, and Ulidiidae, and compared them with larvae of two out‐group families, Rhagionidae and Dolichopodidae, paying particular attention to structures of the head. A set of 86 morphological characters were analysed phylogenetically. The results show that the lower Cyclorrhapha is paraphyletic in relation to the higher Cyclorrhapha. The monophyly of the Cyclorrhapha is strongly supported. The lower Cyclorrhapha is resolved into two clades, based on the Lonchopteridae. Within the Syrphidae the traditional three‐subfamily system is supported, based on the Microdontinae. Within the lower Cyclorrhapha, the larval head is variable in form and arrangement of components. In Lonchopteridae, the mouth lies at the back of an open trough or furrow, comprising ventrally an elongate labium and laterally the maxilla. This arrangement of components appears to facilitate scooping food in water films. In Platypezoidea there is no furrow, and the dorsolateral lobes bearing the antennae are connected by a dorsal extension of the pseudocephalon. The main food‐gathering structure is the hooked apex of the labium, but in Phoridae the mandibles may also be important. In Eumuscomorpha the mandibles are at the apex of the head skeleton. The pseudocephalon is extended and infolded dorsally to form an oral pocket over the mouth. In the Pipunculidae, and the Microdontinae and Syrphinae of the Syrphidae, ventrally it forms a V‐shaped groove or guide along which the mandibles project. The labium is sclerotized apically, and forms a plate or tapered projection. This arrangement of components facilitates holding, piercing and extracting prey tissues. In Eristalinae the pseudocephalon is attached to the mandibles and is formed into a pair of cirri bearing mandibular lobes that lie either side of the mouth. Furthermore, the epipharynx is produced anteriorly in relation to the hypopharynx, and the labium is attached to the anterior part of the epipharynx to form a cavity or atrium. This arrangement is suited to fragmenting and imbibing solid food in Eristalinae with hooked mandibles, and when the mandibles are reduced and the mandibular lobes are inverted and sclerotized, these structures form a filter for separating fluid‐suspended particulate food. In higher Cyclorrhapha an atrium is present as in Eristalinae, but a connection between the pseudocephalon and the mandibles is absent. Instead, the pseudocephalon is bifurcate dorsally and forms a pair of cephalic lobes that ventrally ensheath each mandible. The surface of the sheath may be coated in cirri and other food‐gathering structures. The cephalic lobes, mandibular sheaths and the head skeleton are maneuverable and retractile to a higher degree than in lower Cyclorrhapha. This arrangement of components facilitates feeding on both solid food, in which the mouthooks may extend from the sheath to break the food up, and particulate and suspended food, in which the food‐gathering structures of the sheath scoop up the food. In many higher Cyclorrhapha, maneuverability is enhanced by a break between the labium and the basal sclerite, to which it is fused in all lower Cyclorrhapha. Intermediate characters and states for the structures of the higher cyclorrhaphan larval head are present in out‐groups, and lower Cyclorrhapha and homologies are discussed. Liquidity of the food is an important factor explaining the structure of the larval head in Cyclorrhapha. © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society, 2008, 153 , 287–323.     

Larval development of Lynceus brachyurus (Crustacea, Branchiopoda, Laevicaudata): redescription of unusual crustacean nauplii, with special attention to the molt between last nauplius and first juvenile

The larval development of "conchostracans" has received only scattered attention. Here I present the results of a study on the larval (naupliar) development and the metamorphosis of Lynceus brachyurus, a member of the bivalved branchiopod order the Laevicaudata. Lynceus brachyurus is the only species of the "Conchostraca" in Denmark. The phylogenetic position of the Laevicaudata has traditionally been a source of controversy, and this study does not solve the question completely. This work focuses on features potentially important for phylogeny. The general appearance of the larvae of L. brachyurus has been known for more than a century and a half, and some of its unique features include a large, larval dorsal shield; a huge, plate-like labrum; and a pair of immovable, horn-like antennules. However, many details relating to limb morphology, potentially important for phylogeny, have not been studied previously. Based on size categories, five or six larval stages can be recognized. The larvae approximately double their length and width during development (length: 230-520 microm). Most morphological features stay largely unchanged during development, but the antennal coxal masticatory spines are significant exceptions: they become bifid after one of the first molts. In all larval stages only the antennae and the mandibles actively move. In late naupliar stages the trunk limbs become visible as rows of laterally placed, undeveloped, and still immovable lobes. Swimming is performed by the antennae, whereas the mandibles appear to be involved mainly in feeding, as in other branchiopod larvae. The last naupliar stage undergoes a small metamorphosis to the first juvenile stage, the details of which in part were studied by following the premolt juvenile condition through the cuticle of the last stage nauplius. Among other changes there is a characteristic change in the shape and morphology of the univalved dorsal naupliar shield to a bivalved juvenile carapace. The general morphologies of the antennae and the mandibles are very similar to those of other branchiopod larvae and fall well within the "branchiopod naupliar feeding apparatus" recognized as a branchiopod synapomorphy by Olesen (2003), but some specific features shared with the larvae of other "conchostracans" are also identified. These special "conchostracan" features include: 1) a similar antennular setation; 2) a similar comb-like setulation of the bifid antennal coxal processes; and 3) mandibular palpsetae with setules condensed. In light of recent suggestions concerning branchiopod phylogeny (Cyclestheria as a sister group to the Cladocera), these similarities probably do not support a monophyletic "Conchostraca" but rather are symplesiomorphies of this taxon. A final decision must await a phylogenetic analysis of a more complete set of characters.     

Feeding behavior and related functional morphology of the mayflyEphemerella needhami (Ephemeroptera: Ephemerellidae)

The feeding behavior and functional morphology associated with feeding in Ephemerella needhamiMcDunnough larvae were studied using videomacroscopic techniques, gut content analysis, and scanning electron microscopy. Two stereotypic feeding cycles were employed by the larvae. In the maxillary brushing cycle, the maxillae are the primary food-gathering organs, with the main food being detritus deposited on the filamentous alga Cladophora.In the mandibular biting cycle, the mandibles are the primary food-gathering organs used to bite Cladophora filaments.Epiphytic diatoms on Cladophorawere another important part of the diet. Behavioral similarities are apparent in the choreography and synchronization of mouthpart movements among mayflies from several families. Functional morphological comparisons are drawn with hypognathous E. needhami, Cloeon dipterum, Baetis rhodani,and Siphlonurus aestivalis, aswell as the prognathous Heptageniidae. Differences in mouthpart usage and structure are related to the relative development of setal fields and combs and the feeding microhabitat.     

Effects of diet on female fecundity and larval development in the carrion beetle Necrophila japonica

The carrion beetle subfamily Silphinae (Coleoptera: Silphidae) contains dominant macroinvertebrates of soil ecosystems in temperate zones. However, their feeding habits, which determine the role of each species in the ecosystem, have not been sufficiently studied. Moreover, although a diet shift from necrophagy on vertebrate carcasses to predatory feeding on invertebrates is known to occur in this subfamily, the processes and mechanisms of this shift have also been inadequately addressed. We examined female fecundity and larval development on various diets in a Silphinae species, Necrophila (Eusilpha) japonica (Motschulsky). The experimental diets included a meat diet and various invertebrate diets, which reflect the ‘ancestral’ feeding habit in Silphinae, necrophagy, and the ‘derivative’ feeding habit, predatory feeding. Female fecundity was significantly higher on the meat diet (minced beef) than on an insect larvae diet (mealworms and dipteran larvae) but did not significantly differ from that on an earthworm diet. Larval developmental performance was significantly higher on the earthworm diet than on the meat and insect larvae diets. Our results for larval development were consistent with those of previous stable isotope analyses of the same species, in which isotopic values of larval samples agree with those of hypothetical consumers that utilize earthworms. The consistency of results among different methods indicates that N. japonica larvae are most likely earthworm feeders. In contrast, our results for the female fecundity experiment differed from those of previous stable isotope analyses, in which vertebrate carcasses unlikely serve as the staple diet of adults in the field; thus, the feeding habits of N. japonica adults remain unresolved. Our observations that females and larvae performed best on the meat and earthworm diets, respectively, may indicate that, in Silphinae, the diet shift from necrophagy to predatory habits occurs earlier in larvae than in adults.     

Feeding mechanisms, and their variation in form, of some adult ground-beetles (Coleoptera: Caraboidea)

The structure of the mouthparts and foregut of some caraboid beetles has been correlated with their type of feeding mechanism. These may be adapted to fragmentary feeding, fluid feeding (where pre-oral digestion is important), or to mixed feeding (a large category which ranges from a mainly fluid to a mainly solid intake). Head structures concerned with feeding have been discussed in relation to these methods; they include the mandibles, maxillae, labrum-epipharynx and anterior foregut, proventriculus, labium-hypopharynx and the head floor. Different types of head floor were denned in relation to gular structure, in particular the presence or absence of the mid-gular apodeme. Convergent evolution of feeding mechanisms was noted amongst both fragmentary feeders and fluid feeders; in the latter group, sucking pumps have been evolved in the Carabitae, Scarites , Cicindelidae, Paussini and some other caraboids. It was suggested that head shape in caraboids may reflect locomotory adaptations more frequently than feeding adaptations.     

EVOLUTIONARY LOSS OF LARVAL FEEDING: DEVELOPMENT,FORM AND FUNCTION IN A FACULTATIVELY FEEDING LARVA,BRISASTER LATIFRONS

Species with large eggs and nonfeeding larvae have evolved many times from ancestors with smaller eggs and feeding larvae in numerous groups of aquatic invertebrates and amphibians. This change in reproductive allocation and larval form is often accompanied by dramatic changes in development. Little is known of this transformation because the intermediate form (a facultatively feeding larva) is rare. Knowledge of facultatively feeding larvae may help explain the conditions under which nonfeeding larvae evolve. Two hypotheses concerning the evolutionary loss of larval feeding are as follows: (1) large eggs evolve before modifications in larval development, and (2) the intermediate form (facultatively feeding larva) is evolutionarily short-lived. I show that larvae of a heart urchin, Brisaster latifrons, are capable of feeding but do not require food to complete larval development. Food for larvae appears to have little effect on larval growth and development. The development, form, and suspension feeding mechanism of these larvae are similar to those of obligate-feeding larvae of other echinoids. Feeding rates of Brisaster larvae are similar to cooccurring, obligate-feeding echinoid larvae but are low relative to the large size of Brisaster larvae. The comparison shows that in Brisaster large egg size, independence from larval food, and relatively low feeding rate have evolved before the heterochronies and modified developmental mechanisms common in nonfeeding echinoid larvae. If it is general, the result suggests that hypotheses concerning the origin of nonfeeding larval development should be based on ecological factors that affect natural selection for large eggs, rather than on the evolution of heterochronies and developmental novelties in particular clades. I also discuss alternative hypotheses concerning the evolutionary persistence of facultative larval feeding as a reproductive strategy. These hypotheses could be tested against a phylogenetic hypothesis.     

Morph‐dependent form of asymmetry in mandibles of the stag beetle Prosopocoilus inclinatus (Coleoptera: Lucanidae)

Abstract 1. The form of asymmetry in bilateral organs usually follows the same pattern within single populations. However, some exceptions may occur when a population consists of different phenotypes that are from different ontogenic backgrounds and under different selective pressures. We investigated the asymmetric patterns of mandibles of larvae, females, and males in the stag beetle Prosopocoilus inclinatus. 2. Larval mandibles exhibited directional asymmetry both in length and cross direction, whereas female mandibles showed directional asymmetry in cross direction. These asymmetric structures might be more effective in cutting wood fibres. 3. For the relation of male mandible length to body size, a model with a switch point showed a better fit to the data than a convex curve model. This shows that the males are dimorphic with two distinct morphs. 4. The form of asymmetry in male mandible length differed between the morphs. The smaller males exhibited left‐biased directional asymmetry in common with larvae, whereas the larger males exhibited fluctuating asymmetry. 5. This is a novel finding of a morph‐dependent asymmetry. The morph‐dependent asymmetry in males may be as a result of different selection on each morph or a developmental constraint from larval mandibles to adult ones.     

Comparative morphology of terminal-instar larvae of Cynipoidea: phylogenetic implications

We describe the external morphology of the terminal-instar larvae of 30 species of Cynipoidea (Hymenoptera), with special reference to the head capsule and mouthparts. Twenty-five of the species belong to the Cynipidae and are gall inducers or phytophagous inquilines (guests) in galls, while five represent different insect-parasitic lineages of the Cynipoidea. Although we find only limited variation in body shape, the head sclerites and mandibles offer many characters of potential phylogenetic value. For instance, the mandibles of the parasitoids have one large pointed tooth, with several smaller dents along the inner margin in core figitids, whereas the phytophagous gall inducers and inquilines have mandibles with two or three blunt teeth of subequal size. The mandibles of inquiline larvae are unique in being covered by vertical striations and in having a dominating, broad second tooth. We summarize the qualitative variation among the studied terminal-instar larvae in terms of 33 morphological characters and one life-history trait and examine the phylogenetic implications of these data by running parsimony analyses under uniform character weights and under implied weights (Goloboff weights). The analysis under uniform weights is poorly resolved but the relationships suggested by the implied-weights analysis are largely congruent with previous analyses of adult morphology and molecular data. The larval data support inclusion of the genus Liposthenes in the Neaylax – Isocolus clade, in agreement with the molecular data but in weak conflict with adult morphology. However, the larval data agree with adult morphology and conflict with the molecular data in supporting monophyly of the inquilines.     

Trochophore concepts: ciliary bands and the evolution of larvae in spiralian Metazoa

‘Trochophore’ is a term used in a strict sense for larvae having an opposed-band method of feeding, involving a prototroch and metatroch. Other ciliary bands such as a telotroch and neurotroch may be present. The trochophore has been proposed to represent the ancestral larval form for a group of metazoan phyla (including all members of the Spiralia). The name trochophore is also often applied to larvae that do not conform to the above definition. A cladistic analysis of spiralian taxa (with special reference to polychaete annelids), based on a suite of adult and larval characters, is used to assess several hypotheses: (1) that the trochophore (in a strict sense) is a plesiomorphic form for the Spiralia; (2) that die stricdy defined trochophore is plesiomorphic for members of the Spiralia such as the Polychaeta. The homology of each of the various separate ciliary bands of spiralian larvae, and features such as the apical tuft and protonephridia is also assessed. The results favour the conclusion that the trochophore, if defined as a feeding larval form using opposed bands, should not be regarded as an ancestral (= plesiomorphic) type for the Spiralia, or any other large taxon such as the Polychaeta or Mollusca. The evidence suggests that the various ciliary bands have differing evolutionary histories, and only the Echiura (possibly an annelid group) has members with the classical trochophore. The trochophore is re-defined as a larval form with a prototroch. This broad definition covers a wide variety of larvae, and matches the current usage more accurately than the restricted term. Features such as the neurotroch, telotroch and opposed-band feeding show convergence and reversals. The nature of the metatroch requires further investigation. The presence of a prototroch (and hence trochophore larvae) is used to identify an apomorphy-based taxon, Trochozoa, that includes the first ancestor to have evolved a prototroch and all its descendants. This minimally includes the Annelida [sensu lato), Echiura, Entoprocta, Mollusca and Sipuncula and is a less inclusive taxon than the Spiralia.